Überblick über die Statistik des Gehaltsniveaus für "Legal Affairs Manager in Deutschland"

Speculative application  Skills: Acne, Actinic Keratosis, Acute Myelogenous Leukemia (AML), AIDS, Allergic Rhinitis, Allergy, Alzheimer's, Anaesthetics, Antibiotics, Anti-infectives, Anxiety, arrhythmia, Asthma, Autoimmune diseases, Autoimmune Disorder, Bacterial Vaginosis, Breast Cancer, Cardiology, Cardiovascular, chemotherapy, Chronic Lymphocytic Leukaemia, Chronic Myeloid Leukemia, Chronic Obstructive Pulmonary Disease, Clinical Pathology, CLL, Congestive Heart Failure, COPD, Cosmetics, Cystic Fibrosis, Dementia, Dentistry, Depression, Dermatology, Diabetes, Diagnostics, Dietetics, Endocrine, Endocrinology, Epilepsy, Family Medicine, Fibromyalgia, Gastroenterology, gastrointestinal, Genetic Diseases, GI, Glioblastoma Multiforme (GBM), Gynaecologic, Gynaecology, Gynecology, Haematology, Haemophilia, Heart Disease, Hematology, Hemopure Anemia, Hepatitis, Hepatology, HIV, Hodgkin's disease, Hypertension, IBD, Immunogenicity, Immunopharmacology, Infections, Infectious Diseases, Influenza, Internal Medicine, Joint Replacement, Lymphoma, Mantle Cell Lymphoma, Melanoma, Menopause, Metabolic, Migraine, Multiple Sclerosis, Musculoskeletal, Myelodysplastic Syndrome, Neonatology, Nephrology, Neurodegenerative disorders, Neurology, Neuroscience, NEUROSURGERY, non small cell lung cancer, Non-Hodgkin Lymphoma, nutraceuticals, Nutrition, OA, Obstetrics, Oncology, Ophthalmology, Oral Health, Orphan Diseases, Orphan drug, Orthobiologic Bone graft, Orthopedic Surgery, Orthopedics, Osteoarthritis, Otitis Externa, Otolaryngology, Ovarian Cancer, Paediatric, Pain, Painful Diabetic Neuropathy, Parkinson’s Disease, Physiology, Podiatry, Post-Menopausal Osteoporosis, Primary Immune Deficiency, Primary Sjogren’s Syndrome, Prostate cancer, Prostatic hyperplasia, Psychiatry, Psychology, Pulmonary, Pulmonology, RA, Rare Disease, Respiratory, retinopathy, Rheumatoid Arthritis, Rheumatology, Rhinitis, Rosacea, Schizophrenia, Seasonal Allergic Rhinitis, Severe Hemophilia, Skin Melanoma, Sleep Disorder, Sleep Medicine, Small Lymphocytic Lymphoma, Small Molecule, Smoking Cessation, Solid Tumors, surgery, Systemic Lupus Erythematosus, Systemic Sclerosis, Tissue Ablation, Transplant, Trauma, Traumatology, Type 2 Diabetes Mellitus, Urology, Vaccine, Vaccines, Vascular Diseases, Weight Loss, Women’s Health, Administrative Assistant, Agile Project Manager, Artwork Coordinator, Associate Director Clinical Operations, Associate Project Manager, Auditor, Biomedical Engineer, Biometrics Manager, Biosample Operations Manager, Biostatistician, Biostatistics Associate Director, Brand Team Lead, Business Administration Associate, Business Administration Manager, Business Analyst, Business Development Associate, Business Development Director, Business Development Manager, CEO, Change Manager, Chemical Project Manager, Chemist, Chemistry, Manufacturing & Control Lead (CMC), Chief Financial Officer, Chief Operating Officer, Chief Technical Officer, Clinical Data Associate, Clinical Data Manager, Clinical Data Specialist, Clinical Development Manager, Clinical Engineer, Clinical Lead, Clinical Operations Director, Clinical Operations Manager, Clinical Pharmacologist, Clinical Programmer, Clinical Project Manager, Clinical Research Associate, Clinical Research Director, Clinical Research Manager, Clinical Research Physician, Clinical Research Specialist, Clinical Study Coordinator, Clinical Study Manager, Clinical Supply Coordinator, Clinical Supply Manager, Clinical Trial Assistant, Clinical Trial Educator, Clinical Trial Manager, Clinical Trial Specialist, CMC Manager, Commercial Manager, Communication Manager, Compliance Associate, Compliance Manager, Computer System Validation Specialist, Contract Associate, Contracts Manager, Country Manager, Customer Service Associate, Data Analyst, Data Analytics Assistant, Data Engineer, Data Management Associate Director, Data Management, Manager, Database Programmer_Designer, Demand Planner, Demand Manager, Developer, Diagnostic Specialist, Director of Contracts & Licensing, Dispensary Assistant, Document Specialist, Drug Safety Associate, Drug Safety Director, Drug Safety Manager, Early Access Project Manager, EHS associate, Electronic Data Capture Manager, Electrophysiologist, Employer Engagement Manager, Engineer (out of industry), Epidemiologist, Exploratory Project Manager, Feasibility Manager, Freelance, FSP Clinical Manager, Global Clinical Data Manager, Graduate, Head of Clinical Data Management, Head of Clinical Operations, Head of Risk Management, Health Economist, Health Information Associate, Healthcare Compliance Manager, HR Associate, HR Manager, Imaging Operations Lead, Inhouse Clinical Research Associate, Intern, Investigator, IT Project Manager, Junior Clinical Data Manager, Junior Clinical Research Associate, Junior Pharmacovigilance officer, Junior SAS Programmer, KOL, Laboratory Assistant, Laboratory Manager, Legal Advisor, Licensing Coordinator, Logistics Associate, Logistics Manager, Logistics Supervisor, Manufacturing Manager, Manuscript Editor, Market Access Manager, Market Access Specialist, Market Insights Specialist, Market Research Associate, Marketing Associate, Material Coordinator, Medical Advisor, Medical Assistant, Medical Devices Project Manager, Medical Director, Medical Information Assistant, Medical Information Associate, Medical Information Manager, Medical Manager, Medical Monitor, medical publisher, Medical Representative, Medical Research Associate, Medical Reviewer, Medical Science Liaison, Medical Technologist, Medical Writer, Medico-economic affairs, Meeting Coordinator, MHRA Pharmacovigilance Inspector, Microbiologist, Occupational Therapist, Office Manager, Ophthalmologist, Packaging Associate, Packaging Coordinator, Patient Recruitment Coordinator, Payroll Specialist, Pharmaceutical Physician, Pharmacist, Pharmacokineticist, Pharmacology Director, Pharmacovigilance Manager, Pharmacovigilance Officer, Physiotherapist, Planning analyst, Policy Officer, Post Doctoral Researcher, Preclinical Project Manager, Principal Biostatistician, Principal Scientist, Privacy Officer, Product manager, Production Manager, Production Specialist, Program Development Manager, Programmer Analyst, Programming Associate Director, Project Assistant, Project Manager (other industry), Proposal Developer, Psychiatrist, Psychologist, Publications Manager, QPPV, Qualified Person, Quality Assurance Assistant, Quality Assurance Complaint Specialist, Quality Assurance Director, Quality Assurance Manager, Quality Assurance Specialist, Quality Control Associate, Quality Control Manager, Quality Control Specialist, Quality Engineer, Quality Manager, Quality Specialist, R&D Manager, R&D Project Manager, Record Specialist, Recruitment & Screening Co-ordinator, Registration Specialist, Regulatory Affairs Administrator, Regulatory Affairs Associate, Regulatory Affairs Director, Regulatory Affairs Manager, Regulatory Affairs VP, Regulatory Documentation Scientist, Regulatory Information Specialist, Regulatory labelling specialist, Regulatory Program Manager, Regulatory Site Activation Manager, Remote Site Monitor, Senior, Research Coordinator, Research Funding Manager, Research Team Manager, Resources Manager, Respiratory Physiotherapist, Sales Manager, Sales Rep, Sample Manager, SAS Programmer, Scientific Advisor, Scientific Affairs Associate, Scientist, Senior Associate Supply Chain (GMP), Senior Biostatistician, Senior Clinical Lead, Senior Clinical Research Associate, Senior Clinical Supply Chain Associate, Senior Clinical Team Manager, Senior Clinical Trial Manager, Senior Epidemiologist, Senior Medical Affairs Officer, Senior Nutrition Scientist, Senior Regulatory Affairs Manager, Senior Scientist, Site Engagement Manager, Site Visit Report Reviewer, SOFTWARE DEVELOPER, Software Engineer, Start Up Director, Start-up Manager, Start-Up Specialist, Strategy Lead, Study Authorisation Associate, Study Delivery Operational Specialist, Submissions Manager, Supply Chain Coordinator, Supply Chain Manager, Supply Chain Planner, Surgical Technician, Systems Administrator, Technical Project Leader, Technical Services Specialist, Training Associate, Training Manager, Translator, Validation Engineer, Vendor Manager, Veterinary Nurse, Warehouse Associate, Warehousing & Distribution Leader, BSc, CQA, GMC, MBA, MBChB, MD, MPhil, MRCPsych, MSc, No CRA Certificate, PGDip, Ph.D Statistics, Pharm D, PhD, PRINCE2, Registered Nurse, SAP, Six Sigma, SolTRAQs, Veterinary, 3PL, ADaM, Administration, Adverse Event management, Advocacy plans, Agile, AKTA, Analytical SEC, Animal Health, APICS, Applicant Tracking System Management, APS, ARISg, auditing, Batch release, Batch Review, BHV, Bioequivalence, Bioinformatics, Biologic, Biomarkers, biometrics, Biosamples, Biosimilars, Biostatistics, Biotech, Black Belt, Business Development, C++, Candidate Attraction, CAPA, CDISC, Cell Biology, Cell stem-based therapy, CER, Chemstations, Client communication, Clinical, Clinical Affairs, Clinical Data Management, Clinical Programming, Clinical Research Organisation, Clinical Trial Applications, clinical trials, close out visits, CMC, CMO, Commercialisation, Compassionate Use, Competent Authorities, Computer Systems Validation, Contract, CPIM, CRF Design, CRO, CSR, Data Analysis, data entry, Data Science, Data Warehouse, database design, Datalabs, DHPC, Distribution, Distribution Planning, DMC, Document Management, Downstream, Drug destruction, Drug Development, Drug Safety, DSUR, E2E, Early Access, Early Phase, EC Submissions, ECG, eCRF, EDC, electronic data capture, ELISA, Epidemiology, ePRO, ERP, eTMF, e-TMF, EU Legislation, Eudravigilance, European Federation of Pharmaceutical Industries, Export Management, FDA Audits, Feasibility, Finance, Forecast, FPLC, GCP, GDP, Gene Therapy, Global, Global Regulatory Affairs, GLP, GMP, Government Affairs, GS1 standards, Health Economics, Healthcare, Healthcare Compliance, Healthy Volunteers, Home-based, HPLC, IATA, ICF, ICH-GCP, Imaging, Immunology, IMP, IMPACT, IMPD, Import Management, IND, InForm, Informatics, International, Interviewing, Inventory Management, Investigator Payments, in-vitro, in-vivo, IRB Submissions, IRT, ISO 13485, ISO 13485:2003, ISO 14971, ISO 9001, ISO13485, IVRS, Java, Lab, Labelling, Laboratory, LEAN, Line Management, Logistics, MA-CC, Manufacturing, MAPP, Market Access, Market Insights, Market Intelligence, Market Research, Marketing, Marketing authorizations, Materiovigilance, MedDRA, Medical Affairs, Medical Communication, Medical Devices, Medical Information, Medical Writing, Medidata Rave, Monitoring, Monitoring Visit, MS Office, MS Project, My Trials, NMR, Office-based, Oracle, Outcomes Research, Outsourcing, Packaging, Paediatrics, Patient Outcomes, Permanent, PET scans, Pharma, Pharmaceutical, Pharmacodynamics, Pharmacoeconomics, Pharmacoepidemiology, Pharmacokinetic, Pharmacokinetics, Pharmacology, Pharmacovigilance, Pharmacy, Phase I, pipetting, PMP, Policy, Post Marketing, Postdoctoral research, Post-marketing, Preclinical, Pricing & Reimbursement, Pricing and Reimbursement, PROC, Process Excellence, Procurement, Product Management, Project Leadership, Project Management, PromoMats, Protein Characterisation, protocol development, Protocol writing, PSURs, Public Affairs, publishing, Purchasing, QP, Qualification Visit, Quality Assurance, Quality Control, Quality Management, Quality Management System, Radiology, Randomisation, Randomization, Rave, Reactovigilance, Real World Evidence, Recruitment, Regional Monitoring, Regulatory, Regulatory Operations, Regulatory submissions, Regulatory Systems Management, remote monitoring, RFI, Risk Management, risk-based monitoring, RMA, RMP, SAE, SAE reporting, Sales Inventory, Sample size estimation, Samples, SAS, Scrum, SDS-PAGE, SDTM, Serialisation, Shipments, shipping, Simoa, Site contracts, Site Engagement, site payments, SOX, SPC- CCDS, Spectroscopy, S-Plus, SPSS, SQL, Start-up activities, statistical analysis, Statistics, Study Management, Study Medication Labelling, Sunshine Act, Supplier Qualification, Supply Chain Distribution, Supply Chain Management, Supply Chain Planning, Supply Planning, SUSAR, SUSARs, TMF, Toxicogenomics, Toxicology, Trackwise, Training, Transport Management, Unicorn Purification System, UPLC, Upstream, UV-Vis Spectroscopy, validation, Veeva, Vendor Management, Venipuncture, VISIO, Western Blot, ZINC, Bratislava, Slovakia, Afrikaans, Argentinian, Armenian, Belgian, Bosnian, Bulgarian, Cambodia, Cantonese, Catalonian, Chinese, Croatian, Czech, Danish, Dutch, English, Flemish, French, Greek, Gujarati, Hebrew, Hungarian, Italian, Japanese, Korean, Latvian, Lithuanian, Luxembourgish, Macedonian, Malayalam, Mandarin, Montenegrin, Norwegian, Persian, Punjabi, Romanian, Russian, Serbian, Slovak, Slovene, Slovenian, Spanish, Swedish, Thai, Turkish, UkrainianLocation: GloballyShare: 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Belstaff was created by and for independent spirits. We know that what we do, and who we do it with matters. Join the team and make an impact as we build a legacy that surpasses our incredible past.Love The Challenge. Find A Way. Go All In. Stand Together. Be The Difference.A bit about BelstaffBelstaff is a functional clothing brand founded to move people forward. Throughout our history we have championed material innovation, collaborating with those who challenge the ordinary and celebrate the joy of the journey. Belstaff has designed protective suits for race-car drivers, windproof smocks for Marines and insulating clothing for mountaineers. One thing is at the heart of all these endeavours: An Independent Spirit. Today, this energy prevails and unites the people who bring the Belstaff brand to life, providing the best products to our customers – both old and new. We are committed to building a team of curious, conscious individuals dedicated to showing up, standing together, and being the difference between a good day and a great day.We are searching for a Sales Associate to join our Neumunster team for a full time role, to work 40 hours a week.As Sales Associate you will be at the forefront of establishing and maintaining relationships with clients in order to maximise revenue through the sale of Belstaff products. Along with your team, you will build a strong client base and deliver exceptional customer service including maintaining excellent standards throughout your store. We are looking for someone who will be responsible for;Helping to create and be part of a dynamic and positive team in order to maintain an environment in the store conducive to generating salesGreeting and helping clientsAssisting and anticipating clients on the best products to suit their needs, consistently meeting and exceeding company expectationsConfidentially and professionally answering questions and queries from clientsCross selling across all product offers in store, ensuring the client is walked through the in store collectionMaking the client the main focus at all times and being a role model for a standard that exceeds the benchmark for customer service within the luxury retail industry. This includes being fully conversant with all products and services available including product care, waxing, customisation, aftersales and stock availabilityDelivering after sales services efficientlyBeing up to date on local events and current affairs in order to promote conversation with clientsDeveloping good internal customer service with all other Belstaff Stores and Head OfficeProfessionally handling customer complaints and issuesUnderstanding Belstaff’s Global and International positioningBeing aware of Company and Store Security procedures and adhering to themProtecting stock, being alert to the possibility of theft and following Company procedures to minimise the opportunity for theftMaintaining standards of storing stock on the shop-floor and back of houseParticipating in all audits and countsMaintaining visual merchandising in line with the Belstaff image and the commercial objectives of the storeLiaising with Store Manager, Assistant Store Manager and Supervisor on day to day decisions, regarding safety, profitability and legal issues within the storeBeing aware of and following all company rules and HSE legislationWe are looking for someone who has;a "can-do" attitudean adventurous streakan entrepreneurial spiritan innovative approach to salesstrong commercial awarenessan understanding of how the role contributes to the overall businessWe are looking for someone who is:a great sales person with proven experience in retaila motivated self starter who takes pride in and has achieved great sales figuressomeone who thrives from providing the highest level of customer servicesomeone with the flexibility and drive to help us grow our businesspassionate about Belstaff and you would love to become a brand ambassador a team playerWhere to from here?We are an equal opportunity employer and value diversity at our company. We will not discriminate on the basis of sex, race, marital status, disability, age, sexual orientation or religion. We are committed to a fair and accessible recruitment process for all candidates so if you would like us to make any adjustments to the application or interview process, please let us know and we will be happy to support you. Standort Belstaff, Neumünster

Location: Belgium - Office-basedSchedule: Full Time, Permanent Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for an international CRO can bring? Our team says it's the best of both worlds….   The sponsor-dedicated division of ClinChoice, is searching for a Regulatory Compliance Specialist to join one of our clients, one of the most innovative pharmaceutical companies in the world. ClinChoice is an international CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with their client counterparts.   The Regulatory Specialist assists and supports the Regulatory Affairs department in the execution of regulatory activities to ensure the timely global commercialization of products in compliance with applicable European regulations and international standards.Main Job Tasks and Responsibilities: Partner with the International execution team in the EMEA region.Coordinate, compile, and submit free distribution certificates.Support product registration internationally; Gather and collate information from the manufacturer as required.Provide support to the international team as requested in the development of relationships with RA affiliates, contribute to the development and implementation of the local registration strategy.Act as the EU regulatory Subject Matter Expert for the portfolio under his or her responsibility, supporting the day-to-day Regulatory Affairs activities.Develop strategic guidance and recommend regulatory requirements relevant to the Franchise.Review internal and external communications of the EMEA that refer to products and/or disease state information (Copy Review Process) and represents the department in relevant forums.Advise and provide regulatory impacts to Supply Chain initiatives for the department, be the Primary Point of Contact for the regulatory distribution controls of medical devices and support associated processes and system development.Write, review, and revise company SOPs, recommend efficiencies to processes, and drive Engineering Change Orders (including but not limited to SOPs, and EU labeling approval).Support announced and unannounced inspections by external and internal functions.Assist with organizational tasks: departmental meetings (logistics, formatting, minutes) and department POs, handling regulatory fees (Ariba).Work closely with internal partners across the organisation (including Legal manufacturers, importers, distributors, regional regulatory affairs, quality, supply chain, marketing, and medical affairs) to ensure that stakeholder voices are incorporated into strategies for product launches and product changes.Provide solutions to a variety of problems of moderate scope and complexity where data analysis requires the evaluation of intangible variables.Responsible for the communication of business-related issues or opportunities to the next level of management.Responsible for ensuring personal and Company compliance with all Federal, State, local, and Company regulations, policies, and procedures.Perform other duties assigned as needed.  Education and Experience: University/bachelor's Degree or Equivalent (Science, Engineering, Technical or Biomedical field or Law preferred).4-6 years of work experience in Regulatory Affairs or Quality Affairs preferredSkills:Good knowledge of medical device regulatory requirements in the EUAbility to work effectively in a matrixed organisation and to build partnerships with regional and franchise colleagues.Demonstrate project management skills.Proactive identification of new insights and solutionsExcellent communication, influencing, and presentation skills.Strong output orientation and sense of urgencyExcellent written and verbal communication skills in English (required) The Benefits of Working in Belgium:Competitive SalaryGroup and hospitalisation insuranceElectronic meal vouchersInternet reimbursementCompany Car with fuel card depending on the function.Dedicated Line Manager The Application Process Once you have submitted your CV, you will receive an acknowledgment that we received it. If you have the requirements we need, you will be invited for a phone interview as the first step.  Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.  If you would like to discuss the role before applying through the website @https://www.talentsourcelifesciences.com/jobs   please contact mailto:[email protected] for more information. Who will you be working for?   About ClinChoice      CROMSOURCE is now a ClinChoice Company. ClinChoice is a leading full-service CRO dedicated to offering high-quality one-stop service to the pharmaceutical, biotechnology, medical device and consumer products clients. Some of these services include Clinical Operations, Project Management, Biostatistics, Data Management, Regulatory Affairs, Medical Affairs, and Pharmacovigilance. ClinCHoice has established major delivery centres across US, Canada, China, Europe, India, Japan and the Philippines. It has over 4,000 employees globally, with a strong and talented team, and a growing clinical operations presence across Asia, North America, and Europe.      Our Company Ethos Our employees are the most valuable company asset. We value our resources and ensure they work in a friendly, family environment so they are able to develop their skills and talents. Human Resources is the fulcrum around which all CROMSOURCE activities are built, and close management and training is the core instrument to develop and maintain highly qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology.   The success of these core values is evidenced by our below-industry average turnover rates. Keywords: Regulatory Compliance Specialist, RA, Compliance Specialist, Regulatory Specialist, Medical Devices, Regulatory, Regulatory Affairs, Pharmaceutical, Pharma, CRO, Contract Research Organisation, Outsourced, Sponsor-dedicatedSkills: Regulatory Affairs Associate, CRO, Medical Devices, Outsourcing, Pharma, Pharmaceutical, Regulatory, Regulatory OperationsLocation: BelgiumShare: LinkedIn Facebook Twitter Email

This role required candidate to permanently relocate at Dhahran, Saudi Arabia. About the CompanyThis company engages in the exploration, production, transportation, and sale of crude oil and natural gas. It operates through the following segments: Upstream, Downstream, and Corporate. The Upstream segment includes crude oil, natural gas and natural gas liquids exploration, field development, and production. The Downstream segment focuses on refining, logistics, power generation, and the marketing of crude oil, petroleum and petrochemical products, and related services to international and domestic customers. The Corporate segment offers supporting services including human resources, finance, and information technology. The company was founded on May 29, 1933 and is headquartered in Dhahran, Saudi Arabia. Job Summary We are seeking an experienced and highly qualified event planner, public affairs or public relations professional ("Public Relations Specialist") to coordinate, organize and provide logistics support to the Board and Board Committee meetings of the This Company Board of Directors. This role will sit within the Corporate Secretariat function in the Law Organization of This Company. Headquartered in Dhahran, Saudi Arabia, the successful candidate will join the This Company Secretariat & Governance Legal Practice within the Law Organization's Corporate Secretariat function. In this role, the Public Relations Specialist will support the Corporate Secretary and Assistant Corporate Secretary in organizing and managing logistics support for board and board committee meetings (including site location planning, itinerary development and coordination, travel, entertainment, catering, and other associated activities), as well as handling a broad spectrum of related matters that confront a global energy company. This Company's Law Organization is growing in response to a broad corporate initiative that involves the continued growth of its exploration, production, refining and marketing, along with expansion into petrochemicals, renewables, power and other sectors of the energy business. For adventurous individuals who are interested in working at one of the world's most successful companies, This Company offers a challenging and sophisticated in-house opportunity. Responsibilities: Work with senior executives to develop meeting itineraries and finalize detailed planning for professional corporate events. Coordinate decisions necessary for private, top-quality corporate events. Liaise with business teams, government offices, and global vendors to provide logistics support for board and board committee meetings. Organize presenters and written materials to facilitate seamless information presentation to board directors. Coordinate with IT and manage technology interfaces for senior management and board directors, including online board portal software. Provide additional board support as needed. Perform other duties as assigned by supervising attorneys. Requirements: This role required candidate to permanently relocate at Dhahran, Saudi Arabia. Bachelor's Degree from a recognized and approved university 6+ years of diversified experience with a law firm, large corporation, or other sophisticated business organization Experience in delivering top-quality, professional corporate events across various locations and sectors Experience working with senior management, government officials, and/or a board of directors Strong attention to detail and excellent teamwork, negotiation, and communication skills Proficiency in written and spoken communication principles Bonus qualifications: Experience in the energy industry (oil and gas, petrochemical, power, or oil field services), public company experience, and international experience. Standort MatchaTalent, Hamburg

This role required candidate to permanently relocate at Dhahran, Saudi Arabia. About the CompanyThis company engages in the exploration, production, transportation, and sale of crude oil and natural gas. It operates through the following segments: Upstream, Downstream, and Corporate. The Upstream segment includes crude oil, natural gas and natural gas liquids exploration, field development, and production. The Downstream segment focuses on refining, logistics, power generation, and the marketing of crude oil, petroleum and petrochemical products, and related services to international and domestic customers. The Corporate segment offers supporting services including human resources, finance, and information technology. The company was founded on May 29, 1933 and is headquartered in Dhahran, Saudi Arabia. Job Summary We are seeking an experienced and highly qualified event planner, public affairs or public relations professional ("Public Relations Specialist") to coordinate, organize and provide logistics support to the Board and Board Committee meetings of the This Company Board of Directors. This role will sit within the Corporate Secretariat function in the Law Organization of This Company. Headquartered in Dhahran, Saudi Arabia, the successful candidate will join the This Company Secretariat & Governance Legal Practice within the Law Organization's Corporate Secretariat function. In this role, the Public Relations Specialist will support the Corporate Secretary and Assistant Corporate Secretary in organizing and managing logistics support for board and board committee meetings (including site location planning, itinerary development and coordination, travel, entertainment, catering, and other associated activities), as well as handling a broad spectrum of related matters that confront a global energy company. This Company's Law Organization is growing in response to a broad corporate initiative that involves the continued growth of its exploration, production, refining and marketing, along with expansion into petrochemicals, renewables, power and other sectors of the energy business. For adventurous individuals who are interested in working at one of the world's most successful companies, This Company offers a challenging and sophisticated in-house opportunity. Responsibilities: Work with senior executives to develop meeting itineraries and finalize detailed planning for professional corporate events. Coordinate decisions necessary for private, top-quality corporate events. Liaise with business teams, government offices, and global vendors to provide logistics support for board and board committee meetings. Organize presenters and written materials to facilitate seamless information presentation to board directors. Coordinate with IT and manage technology interfaces for senior management and board directors, including online board portal software. Provide additional board support as needed. Perform other duties as assigned by supervising attorneys. Requirements: This role required candidate to permanently relocate at Dhahran, Saudi Arabia. Bachelor's Degree from a recognized and approved university 6+ years of diversified experience with a law firm, large corporation, or other sophisticated business organization Experience in delivering top-quality, professional corporate events across various locations and sectors Experience working with senior management, government officials, and/or a board of directors Strong attention to detail and excellent teamwork, negotiation, and communication skills Proficiency in written and spoken communication principles Bonus qualifications: Experience in the energy industry (oil and gas, petrochemical, power, or oil field services), public company experience, and international experience. Standort MatchaTalent, Frankfurt

We are recruiting an Associate Director Market Access Germany, in which through market access activities the successful candidate will contribute to shape the German market landscape to accept differentiation and create an enhanced positioning for cell-culture and adjuvanted vaccines accepted by payers and by key stakeholders. You will design, develop and implement effective market strategies related to new launches and existing products in the area of pricing and reimbursement, evidence-based medicine review, health technology, and/or health economic modelling (this latter in close collaboration with global and EMEA market access). You will communicate the unique attributes of CSL Seqirus portfolio to external stakeholders to ensure the vaccine's value proposition will be recognized and maximize market uptake. To be successful in this position you will work collectively with national and regional payers, physician associations, pharmacy associations, reimbursement influencers and other decision makers to ensure continuous changing reimbursement systems remain fair to all involved parties and the value of the Seqirus portfolio is recognised. You will actively drive, support and contribute to internal business strategic meetings, budget reviews, HTA submissions, and be the owner of key strategic projects, such as regional and national market access advisory boards, price submissions, health economic analysis and budget impact model tools This role reports to the Country Head DACH, and is a strategic role which requires very close cross-collaboration; locally with medical, marketing, sales teams, and globally with market access team, policy team, Responsibilities include: - Responsible for planning and implementing market access strategy for the Seqirus existing portfolio as well as preparing for new launches Works cross functionally with the country head, with the local marketing, medical and policy colleagues as well as with the global and EMEA market access teams and other key stakeholders to develop the value propositions for the portfolio. Engage key stakeholders as sounding board to validate and optimise the market access strategy Work closely with the global and EMEA market access teams to generate health economic analysis, cost effectiveness and budget impact models in line with the country strategy Provide input into policy shaping dossiers preparation, supporting the achievement of differentiated positioning for the Seqirus innovative vaccines In collaboration with the cross-functional team, generate compelling story flows able to effectively communicate information on product efficacy, on RWE data, on health economics and value propositions to demonstrate advantages of our vaccines Monitors the external environment, customers, and competitors to understand market conditions and identify opportunities to improve value capture. Identify any legislation changes that can have an impact on price and reimbursement and on access in general Input to the future pricing strategy for new launches together with the cross functional team Evaluates pricing and market access risks Take care of annual submission of pricing and price update in the official portals; Builds and maintains relationships with key regional and national key stakeholders, health economic opinion leaders, payers and healthcare groups Engage at regional level with payers, with physician (KV) and pharmacy associations to continue enhance awareness on Seqirus expertise and its portfolio, shape conversations to create acceptance for Seqirus innovative vaccine. Implement strategies and tactics to avoid the barrier of the economic principle, leading as many regions as possible to include cell-culture and adjuvanted under the pricing acceptable new vaccines Ensure frequent meetings with payers and KVs, coordinate meeting to include medical and the GM Develop and execute market access advisory boards, round tables Provide regular update on the changing market access landscape, or new regulations that can affect access keeping the cross-functional team informed Have a close collaboration with EMEA market access and global team, collaborate on the development of HE models, budget impact models and other access tools Create dash boards and update overview to inform the cross-functional team as well as the sales team; collaborate with the regional sales managers and district managers to optimise the communication flow and ensure optimised strategy and results at regional level Input into country strategic meetings, business reviews and budget planning Coordinate market access meetings with medical affairs, ensuring key messages and strategy are always considering the latest stand of the portfolio evidence generation Collaborate closely with policy colleagues and agencies to support achieving a STIKO differentiated recommendation for the Seqirus portfolio Ensure compliance with all internal and external policies, procedures, and regulations e.g., Code of Practice, financial processes Qualifications, skills, and Experience: - Bachelors’ degree in business, health policy, health economics, life sciences or healthcare discipline; 10 years' pharmaceutical industry experience including market access, brand/specialty channel marketing and account management. Must have knowledge of the German healthcare system, relevant legal, compliance and regulatory requirements. Fluent in German and English Holds a driving license valid in Germany. Willing to travel across Germany and internationally according to business needs. Excellent oral and written communication skills in German and English language required. Ability to engage stakeholders at any level Excellent and demonstrated interpersonal skills: Collaborate effectively and demonstrate leadership and teamwork with peers, internal stakeholders and external customers that inspire alignment and partnership on a shared vision or strategy. Be a self-starter, be accountable and have a sense of urgency in delivering results that have payors impact and yield a positive customer experience. Our Benefits We encourage you to make your well-being a priority. It’s important and so are you. Learn more about at CSL. About CSL CSL is a leading global biotechnology company with a dynamic portfolio of life-saving medicines, including those that treat haemophilia and immune deficiencies, as well as vaccines to prevent influenza. Since our start in 1916, we have been driven by our promise to save lives through innovation. Learn more about . We want CSL to reflect the world around us As a global organisation with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about at CSL. Do work that matters at CSL! Standort 0115 Seqirus GmbH, Marburg

Das sind Ihre neuen Aufgaben Von der Planung bis zur Durchführung und Bewertung betreuen Sie die regulatorischen und wissenschaftlichen Aufgaben zur Erbringung der notwendigen klinischen Nachweise für unsere IVD-ProdukteFür die Entwicklung und Leistung unserer IVD-Produkte ermitteln Sie klinische bzw. diagnostische KriterienSie erarbeiten produktspezifische klinische Bewertungsstrategien inkl. statistischer Elemente bei der Planung klinischer Leistungsstudien, stellen die Einhaltung der Pläne sicher, bewerten Änderungen, werten resultierende Daten entsprechend aus und fassen die Ergebnisse in Berichten für die technische Dokumentation zusammenBei der Durchführung der Leistungsstudien stellen Sie die Einhaltung regulatorischer und ethischer Anforderungen sicherDarüber hinaus sind Sie bei der Weiterentwicklung unserer Prozesse zur klinischen Leistungs bewertung sowie zur Analyseleistung beteiligtFür Ihre Kollegen in anderen Fachbereichen, z.B. Entwicklung und Produktmanagement, sind Sie wichtiger Ansprechpartner für Fragestellungen zu Leistungsdaten und durchgeführten Studien Das zeichnet Sie aus Ihr Masterstudium der Ingenieur- oder Naturwissenschaften wie z. B. Medizintechnik, Biologie oder Biotechnologie haben Sie erfolgreich abgeschlossen und idealerweise um eine Promotion im Fachgebiet Immunologie ergänztSie bringen mehrjährige Berufserfahrung im regulatorischen Bereich eines IVD- oder MDR-Herstellers und der Durchführung von analytischen und klinischen Studien mit; idealerweise können Sie zusätzlich Erfahrung mit dokumentierter Literaturrecherche und Statistik vorweisenMit Ihrem analytischen Denkvermögen und Ihrer strukturierten Arbeitsweise fällt es Ihnen leicht, komplexe Sachverhalte schnell zu erfassen und aufzubereitenIhre sehr guten Deutsch- und Englischkenntnisse wenden Sie bei der Dokumentation und im Austausch mit unseren ausländischen Niederlassungen sicher anDank Ihrer Kommunikationsstärke und einem ausgeprägten Teamgeist können Sie zwischen den Fachabteilungen gut vermitteln und Ihren Kollegen als kompetenter Ansprechpartner stets weiterhelfen Das erwartet Sie Ein sicherer Job für die Zukunft - Unbefristete Arbeitsverträge in einer krisensicheren und zukunftsorientierten BrancheEin gutes Gleichgewicht zwischen Beruf und Freizeit - Flexible Arbeits- und Pausenzeiten rund um die Kernarbeitszeit, Stundenkonto, 30 Urlaubstage, mobiles Arbeiten (nach Absprache möglich)Kollegen, bei denen man sich wohl fühlt - Familiäre Arbeitsatmosphäre, Du-Kultur auf allen Ebenen, Onboarding und Patenprogramm, TeameventsGute Arbeit zahlt sich aus - 13 Gehälter, Mitarbeiterempfehlungsprogramm, übergesetzliche Zuschüsse zu Ihrer AltersvorsorgeGesundheit ist das höchste Gut - Ausgewogene Ernährung im Betriebsrestaurant, Getränkeflatrate, Betriebsarzt, Physioservice und Massagen, diverse FirmensportgruppenViel Abwechslung, auch nach Feierabend - Mitarbeiterveranstaltungen, Kreativ-Workshops, Sonderkonditionen für Veranstaltungen, Rabattaktionen für Produkte und DienstleistungenFeedback, das gehört wird - Jährliche Mitarbeitergespräche, regelmäßige MitarbeiterbefragungenUnd vieles mehr! Standort EUROIMMUN Medizinische Labordiagnostika AG, Lübeck

Job IntroductionWe have an exciting (and challenging) opening for a User Helpdesk Operator in Darmstadt. The position is offered as fixed-term contract until 30/06/2025.Dynamic, Energetic, Entrepreneurial, Highly Motivated, Resilient … If this describes you then we would love to hear from you :) Come and join talented diverse Serco team at the European Organisation for the Exploitation of Meteorological Satellites (EUMETSAT) based in Darmstadt, Germany. Discover the offer below and click on ‘Apply’ if you know that your skillset and talents are a suitable match for this opportunity.Serco – The employer of choice for a career within the Space Sector.Serco are a trusted provider of services to National Space Agencies and the European Space Agency (ESA), we have over 40 years’ experience supporting the space sector and providing services for all stages of our customer’s space missions.Join our community of space specialists across EuropeWe are proud to support the European institutional Space landscape: Serco boasts an extensive network of Space professionals located at our offices in Darmstadt, Noordwijk, Frascati, Paris and Madrid, all within close proximity of our two largest space sector customers, European Space Agency/European Space Operations Centre (ESA/ESOC) and European Organisation for the Exploitation of Meteorological Satellites (EUMETSAT).Supporting Women in AerospaceDiversity and Inclusion is extremely important to us. Supporting women's opportunities, development and visibility in the space sector is key and that is why we are proud members and supporters of Women in Aerospace Europe, a dynamic and global network supporting women's careers in Aerospace.Women in Aerospace Europe (WIA-E) – Supporting women in STEM (wia-europe.org) Main ResponsibilitiesThe User Helpdesk Support is an essential interface to the external user community and a key element supporting the enhancement of EUMETSAT’s reputation in the eyes of its external users. The main aim of the User Helpdesk Support is to provide a one-stop-shop for EUMETSAT’s user community by providing an enquiry processing and user registration service. The ideal candidate shall perform the day-to-day activities of the User Helpdesk at EUMETSAT, these tasks include the following:1. User Enquiry Tasks:Registering and tracking user enquiries using a database system;Corresponding with EUMETSAT's user community primarily by e-mail and occasionally by telephone to assist users with their enquiries:Responding directly to the user for simple (off-the-shelf) enquiries in accordance with agreed service specifications and working practice;Assigning internal and external actionees (experts) to provide input for detailed (bespoke) enquiries;Relaying and reformatting the feedback from actionees to the end user and conveying received user feedback to the appointed actionee;Interacting with external helpdesk services within partner organisations to transfer and to receive user enquiries;Monitoring the progress of the all open enquiries until completion, i.e. following up with actionees on their assigned tickets.2. User Registration Tasks:Registering users of data services in a database and assigning services to these users as per their registration;Interacting with experts in the Legal Affairs and Finance Divisions where relevant (i.e. as part of the data licensing and decryption hardware and software payment process);Dispatching decryption hardware and software to users;Monitoring the progress of all open registrations until completion.3. Provision of imagery and analysis support to the International Charter Space and Major Disasters:Circulating incoming requests for satellite imagery to the relevant internal teams;Uploading the resulting imagery to the Charter online tool;Assisting in the recording of Charter Project Manager feedback and Charter end user feedback.4. User Interaction Administration Tasks:Recording and filing correspondence and documentation related to user interactions;Maintaining the content of reports used for analysing user enquiries against agreed service level targets;Maintaining the user contact details and profiles in databases and registration systems and providing inputs to future enhancements of these systems;Assisting in the preparation of customer surveys and the recording of results;Maintaining User Service Helpdesk working practice documentation.5. Attendance at Daily Operations Meetings:Attending operational morning briefings to be aware of events/anomalies effecting the EUMETSAT operational services and to report, as needed, on user feedback received relating to these events/anomalies.The activities of the User Helpdesk Support will involve a significant amount of liaison with other personnel at EUMETSAT as well as partner organisations.Successful CandidateDo you think you are the person we are looking for? See below what experience or knowledge you should bring:Proven experience in using MS Office, including familiarity with the use of MS Word, MS Excel spreadsheets and MS Outlook.Fluency in both spoken and written English.Experience in working within a team.Experience in working as a first-line interface with customers, including responding to customer questions.Experience in using a ticketing tool or equivalent to record customer enquiries or feedback.Interpersonal skills necessary to ensure responses to customers are handled in a professional manner. About The CompanyWhy should you join Serco ?At Serco not only is the nature of the work we do important, everyone has an important role to play.Meaningful and vital work - You’ll contribute to methodologically intercepting challenges whilst achievements will also be recognised and celebrated.A world of opportunity - You’ll be wholeheartedly supported with development and career progressionGreat people - You’ll become an integral member of a well-defined and supportive team who believe passionately in the value of our work. We are a company passionate about diversity and inclusion. About SercoSerco provides the User Helpdesk and Data Centre Operations Service of the European Organisation for the Exploitation of Meteorological Satellites (EUMETSAT), which plays a key role in enhancing the use of EUMETSAT data, products and data services.The main objective of the service is to ensure effective and user-driven service to support the provision of data, both real-time and offline, as well as to provide comprehensive technical information to support all forms of user enquiries relating both to current operational services and to future satellite programmes of EUMETSAT.Important:Any offer of employment is contingent upon you providing documents to verify your identity and employment eligibility, as required by law.Applicants are reminded that they will be requested to produce such documentation during the recruitment process.Please contact a member of the recruitment team if you require further details of acceptable types of documentation required for verification of identity and work authorization. Data Protection:For more information on how the personal data in your application is process, please see the link Data Protection policy here. Package DescriptionWhat we offer if you join our amazing team:• Competitive Salary • Corporate Benefits Package • Support provided to EU Nationals requiring relocation – Information available upon request• Company eventsÜber das Unternehmen:Serco Europe

User Helpdesk Operator (EUMETSAT)Serco is a leading Space Services Provider with thousands of skilled resources that has supported over 50 space missions on behalf of more than 10 Space or Government agencies around the globe, including the ESA and NASA. Serco offers space capability across the full space lifecycle from satellite testing to Launch services, LEOP to spacecraft operations, space surveillance to data management, and supporting downstream application development. With over 55 years history in the space sector Serco is well placed to contribute to National strategies and New Space ventures who want to scale their businesses/organizations with skilled talent.On behalf of our customer EUMETSAT, we are looking for a User Helpdesk Operator to join our team and work on site at our client, in Darmstadt. The User Helpdesk Support is an essential interface to the external user community and a key element supporting the enhancement of EUMETSAT’s reputation in the eyes of its external users. The main aim of the User Helpdesk Support is to provide a one-stop-shop for EUMETSAT’s user community by providing an enquiry processing and user registration service. The ideal candidate shall perform the day-to-day activities of the User Helpdesk at EUMETSAT.The position is offered as a fixed-term contract until 30/06/2025. Responsibilities:User Enquiry tasks:Registering and tracking user enquiries using a database systemCorresponding with EUMETSAT's user community primarily by e-mail and occasionally by telephone to assist users with their enquiries:Responding directly to the user for simple (off-the-shelf) enquiries in accordance with agreed service specifications and working practice.Assigning internal and external actionees (experts) to provide input for detailed (bespoke) enquiries.Relaying and reformatting the feedback from actionees to the end user and conveying received user feedback to the appointed actionee.Interacting with external helpdesk services within partner organisations to transfer and to receive user enquiries.Monitoring the progress of the all open enquiries until completion, i.e. following up with actionees on their assigned tickets.User Registration Tasks:Registering users of data services in a database and assigning services to these users as per their registration.Interacting with experts in the Legal Affairs and Finance Divisions where relevant (i.e. as part of the data licensing and decryption hardware and software payment process).Dispatching decryption hardware and software to users.Monitoring the progress of all open registrations until completion.Provision of imagery and analysis support to the International Charter Space and Major Disasters:Circulating incoming requests for satellite imagery to the relevant internal teams.Uploading the resulting imagery to the Charter online tool.Assisting in the recording of Charter Project Manager feedback and Charter end user feedback.User Interaction Administration Tasks:Recording and filing correspondence and documentation related to user interactions.Maintaining the content of reports used for analysing user enquiries against agreed service level targets.Maintaining the user contact details and profiles in databases and registration systems and providing inputs to future enhancements of these systems.Assisting in the preparation of customer surveys and the recording of results.Maintaining User Service Helpdesk working practice documentation.Attendance at Daily Operations Meetings:Attending operational morning briefings to be aware of events/anomalies effecting the EUMETSAT operational services and to report, as needed, on user feedback received relating to these events/anomalies.The activities of the User Helpdesk Support will involve a significant amount of liaison with other personnel at EUMETSAT as well as partner organisations.Profile:Proven experience in using MS Office, including familiarity with the use of MS Word, MS Excel spreadsheets and MS Outlook.Fluency in both spoken and written English.Experience in working within a team.Experience in working as a first-line interface with customers, including responding to customer questions.Experience in using a ticketing tool or equivalent to record customer enquiries or feedback.Interpersonal skills necessary to ensure responses to customers are handled in a professional manner.Within Serco we believe there is a place here for everyone. Diversity & Inclusion at Serco is based on a culture where every voice is heard, and every employee feels valued. Working together as one team, we can enhance the experience of our people and teams, improve the value of our solutions to better serve the missions of our customers, and make a difference in our world. We are enthusiastic and passionate about our work which is infectious. We allow our employees to take responsibility for their work and promote a positive working culture.What we offer:Competitive Salary.Corporate Benefits Package.Support provided on relocation – Information available upon request.Company Events.About Serco:Serco is a leading Space Services Provider with thousands of skilled resources that has supported over 50 space missions on behalf of more than 10 Space or Government agencies around the globe, including the likes of ESA, CNES, EUMETSAT, EUSPA, ASI and NASA.We offer space capabilities across the full space lifecycle from satellite testing to Launch services, LEOP to spacecraft operations, space surveillance to data management, and supporting downstream application development. With over 55 years history in the space sector Serco is well placed to contribute to National strategies across Europe and the globeWe work within the heart of the space sector so understand the challenges our customers face. When it comes to recruitment we are experts in sourcing the very best talent within space engineering, earth observation, satellite communications and cyber security. We have placed hundreds of people from post graduates through to C-suite executives into space agencies, satellite operators, manufacturers, system integrators, consultancies, earth observation/remote sensing, launch providers and much more. Über das Unternehmen:Serco

If you are a Jazz employee please apply via the Internal Career siteJazz Pharmaceuticals plc (NASDAQ: JAZZ) is a global biopharmaceutical company whose purpose is to innovate to transform the lives of patients and their families. We are dedicated to developing life-changing medicines for people with serious diseases - often with limited or no therapeutic options. We have a diverse portfolio of marketed medicines and novel product candidates, from early- to late-stage development, in neuroscience and oncology. We actively explore new options for patients including novel compounds, small molecules and biologics, and through cannabinoid science and innovative delivery technologies. Jazz is headquartered in Dublin, Ireland and has employees around the globe, serving patients in nearly 75 countries. For more information, please visit www.jazzpharmaceuticals.com and follow @JazzPharma on Twitter.Overview:Jazz Pharmaceuticals is an international biopharmaceutical company focused on improving patients’ lives by identifying, developing and commercializing meaningful products that address areas of unmet medical need. We are continuing to expand our commercial product portfolio and our research and development pipeline in therapeutic areas that can leverage our unique expertise. Our therapeutic areas of focus include neuroscience and hematology/oncology – areas in which we have a deep understanding of the patient journey and a suite of products and product candidates to address critical needs.Brief Description:Reporting to the Country Medical Director for Germany, the Medical Director Oncology is responsible for the development and delivery of the Country Medical Affairs strategy and programs that support the successful development and commercialisation of Jazz Pharmaceuticals products in the hematology/oncology franchise. The incumbent will be responsible for building and leading the Hematology/Oncology Medical Affairs department. He/she will be positioned as the Medical expert lead to both internal and external audiences.The role will demand strong leadership qualities, high levels of cross functional collaboration and the ability to influence across all levels of the organization. The incumbent will need to balance the requirement for strong strategic thinking with a need to execute in a fast moving organization.The incumbent is responsible for ensuring all activities are executed in accordance with regulatory and legal frameworks of the country as well as Jazz Pharmaceuticals Policies and Healthcare compliance procedures.Essential FunctionsLeadership of Hematology/Oncology Medical Affairs DELead, develop and build a high performing Medical Affairs Team (Field-Team and Office-Team)Manage, coach and develop Medical Affairs personnelRole model and exemplify Jazz Cultural valuesBe a strong strategic partner to cross functional colleagues including Commercial and Market AccessEnsure systems, processes and ways of working are in place to facilitate:Effective execution of the medical planDevelopment and maintenance of a high level of knowledge of hematology/oncology medicine related clinical and scientific literature in order to position themselves and the team as experts in the field.Effective planning and utilization of national Key External Experts (KEE)Data generation activities including reactive support of Investigator Sponsored Trial requestsSupport development of partnerships with KEEs through the provision of balanced, scientific information and ensure that decision makers have the appropriate information to position the Jazz portfolio in treatment guidelines and protocols.High standards with regards to PV, compliance and SOPsReview and approval of medical and marketing materials and activities in line with national regulationsDelivery of quality medical information to internal and external customersStrategic and Tactical PlanningEnsure development and delivery of the DE Hematology/Oncology Medical Affairs strategy and plan in close collaboration with business partners and aligned to the EU/RoW strategySet departmental SMART objectives and track, measure and report progress of plans and budgetsEnsure the business needs are effectively communicated to partners in the EU/RoW regional office, so that there is alignment on strategy and plans at all levels External Relationships Develop influential relationships with National Key External Experts through the provision of balanced, scientific information and ensure that decision makers have the appropriate information to position the Jazz portfolio in treatment guidelines and protocols.Attend appropriate scientific congresses to stay abreast of developments and to support National KEE activitiesSupport development of Jazz EU/RoW positioning as the scientific authority on hematology/oncology medicine and support national KEE advocacy through provision of scientific and clinical information via the MSL teamRequired Knowledge, Skills, and Abilities Minimum of 4 years of medical affairs experience in the pharmaceutical industry essentialPrevious line-management experience a plusExperience in hematology/oncologyDeep understanding of the German healthcare systemStrong leadership skills with demonstrable ability to influence at all levels of the organization. Strong inter-personal relationship building skills/collaboration and teamworkAbility to critically analyse complex dataExcellent communication skills, including strong presentation skillsExperience in establishing strong partnerships with academic and patient advocacy societiesFlexible, independent, and proactive working style.Willingness to travel frequentlyExcellent command of spoken and written German and EnglishRequired/Preferred Education and LicensesGraduate with a higher scientific qualification in the life sciences e.g. MD, Pharm D, MSc, PhD. MD preferredJazz Pharmaceuticals is an Equal Opportunity Employer.

Job Description Nordberg Medical is seeking a Medical Affairs Manager DACHAs a Medical Affairs Manager DACH, your role involves providing medical and scientific support for Nordberg Medical’s product. You will act as a subject matter expert for external stakeholders, including key opinion leaders, healthcare professionals, regulatory bodies, and patient advocacy groups. Reporting to the European Medical Affairs Director (with a dotted line to the VP Commercial Operations Central Europe) you will play a pivotal role in supporting the company's growth and expansion efforts. Key Responsibilities include but are not limited to:Strategic and Tactical LeadershipReview scientific literature (mostly medical aesthetics) to inform company strategy, consolidating actionable medical insights. Develop regional medical affairs goals, translating them into tactics for optimal scientific exchange. Manage Key Opinion Leader (KOL) relationships and support faculty development activities. Support clinical research (ISS and SIS) by identifying investigators, managing protocols, and reviewing study data. Ensure compliance with local regulations and review promotional materials. Medical and Scientific LeadershipProvide local scientific perspective to Regional Medical Affairs team.Build relationships with external scientific community and scientific societies. Attend and present at scientific meetings and conferences. Support development of medical educational programs and advisory boards.Regulatory SupportCollaborate with regulatory affairs for submissions and product approvals.Maintain knowledge of regulatory guidelines and assist in resolving regulatory issues.

Job Description Ben jij een ambitieuze professional met expertise in elektrische installaties? Bij Imtech Building Technics in Brussel zoeken we een gedreven Project Manager Elektriciteit om ons Buildings-team te versterken. Onze vestiging is gespecialiseerd in het realiseren van complete elektrische installaties voor kantoren, ziekenhuizen, woonzorgcentra, datacenters, logistieke en semi-industriële gebouwen. Als Project Manager Elektriciteit speel je een cruciale rol in het succesvol uitvoeren van onze projecten. Lees verder om te ontdekken hoe jij kunt bijdragen aan innovatieve en kwalitatieve oplossingen in de gebouwentechniek. Jouw verantwoordelijkheden omvatten:Het organiseren, plannen en controleren van alle activiteiten met betrekking tot jouw projecten.Het vertegenwoordigen van ons bedrijf bij klanten en partners.Het leiden en motiveren van een bekwaam team van medewerkers per project binnen C-tech.Eindverantwoordelijkheid dragen voor jouw projecten in uitvoering, zowel technisch als financieel.Zorg dragen voor het tijdig leveren van betrouwbare, geteste systemen met de vooropgestelde kwaliteit, met optimale inzet van middelen.Zowel technische, organisatorische als commerciële uitdagingen doortastend aanpakken en oplossen.Als jij klaar bent voor deze boeiende uitdaging in de bruisende omgeving van Brussel, dan nodigen we je uit om verder te lezen en te ontdekken hoe jij kunt bijdragen aan ons succesverhaal in de wereld van gebouwentechniek. Wat we zoekenDiploma. Je hebt een Master- of bacheloropleiding elektriciteit of elektromechanica of gelijkwaardig door ervaring.Ervaring. Je hebt minstens 5 jaar ervaring.Goede kennis van het Nederlands en Frans. Engels is een pluspunt.Soft skills. Je bent een klantgerichte en assertieve persoonlijkheid met sterke commerciële en sociale vaardigheden.Teamplayer. Je beschikt over de kwaliteit om je collega's te motiveren en samen met hen aan de slag te gaan.Communicatie. Je hebt de vaardigheid om je ideeën, standpunten en boodschappen op een heldere, overtuigende en gestructureerde manier te communiceren naar verschillende stakeholders.Empathisch vermogen. Je bent in staat om jezelf in anderen te verplaatsen en hun perspectieven en gevoelens te begrijpen.Flexibiliteit. Je hebt een sterk aanpassingsvermogen en bent in staat om snel te reageren en je aan te passen aan nieuwe omstandigheden wanneer deze zich voordoen.Gedrevenheid. Je hebt een proactieve “make it happen”-mentaliteit en bent eindeloos energiek. Je bent doel- en resultaatgericht en hebt het vermogen om kalm te blijven in stresssituaties.Plezier. Je hebt plezier in je werk en straalt dat uit naar je team en collega's. Je hebt een optimistische instelling en bent in staat om kansen te zien, zelfs in uitdagende situaties.Als je niet volledig aan alle gestelde eisen voldoet, maar toch het sterke gevoel hebt dat je de perfecte kandidaat bent voor deze functie, moedigen we je zeker aan om te solliciteren. Bij ons waarderen we initiatief en out-of-the-box denken. We geloven dat diversiteit in achtergronden, vaardigheden en perspectieven ons team verrijkt. Dus als je denkt dat je een waardevolle bijdrage kunt leveren, horen we graag van je en staan we open voor het verkennen van de mogelijkheden.Wat we aanbiedenCompetitief salarispakket. Wij bieden een competitief salarispakket aan gekoppeld aan heel wat extra’s inclusief laptop met professionele software, gsm, benefits@work, Buddyfit, enz.Flexibiliteit. Bij Cordeel Group is het geen "clock in, clock out" bedrijf. Daarom is werken op afstand en flexibele werktijden volledig acceptabel. We waarderen de mogelijkheid om werk-privébalans te creëren en begrijpen dat flexibiliteit belangrijk is voor het welzijn en de productiviteit van onze medewerkers.C-Academy. Bij Cordeel Group hechten we veel belang aan jouw persoonlijke ontwikkeling. Samen stellen we een ontwikkelingsplan op en bieden we je de kans om je talenten verder te ontwikkelen en samen te groeien.Snelheid. Cordeel Group is een team van slimme, snelwerkende en gepassioneerde professionals die zich inzetten voor “Transforming the future as the fastest builder by focussing on innovation to create smart, energy-efficient and low-carbon solutions”. Door deel uit te maken van ons team, laat je ons zien dat je in staat bent om te multitasken en prioriteiten te stellen op de meest efficiënte en effectieve manier.Geen micromanaging. Bij Cordeel Group ben je de eigenaar van je inspanningen - vanaf dag één maak je deel uit van het team en vertrouwen we erop dat je de verantwoordelijkheid neemt voor je taken. Hulp en ondersteuning zullen er zijn wanneer gevraagd en nodig, maar je hebt alle stimulans en mogelijkheden om een echte impact te maken.Unieke groeimogelijkheden. Cordeel Group is een toonaangevende groep van meer dan 50 bedrijven. Wij bieden je een stimulerende en uitdagende functie waarin je de mogelijkheid hebt om zowel binnen je afdeling als binnen het bredere bedrijf te groeien. Bij het openen van een nieuwe functie geven we altijd voorrang aan interne talenten binnen ons bedrijf.Tonnen leuke activiteiten. We organiseren te gekke teambuildings, activiteiten, borrels en regelmatig bedrijfswijde netwerkevenementen.Vous êtes un professionnel ambitieux avec une expertise dans les installations électriques ? Chez Imtech Building Technics à Bruxelles, nous sommes à la recherche d'un Project Manager Electricity motivé pour rejoindre notre équipe Buildings. Notre bureau est spécialisé dans la réalisation d'installations électriques complètes pour des bureaux, des hôpitaux, des centres de soins résidentiels, des centres de données, des bâtiments logistiques et semi-industriels. En tant que Project Manager Electricity, vous jouerez un rôle crucial dans l'exécution réussie de nos projets. Lisez la suite pour découvrir comment vous pouvez contribuer à des solutions innovantes et de haute qualité dans le domaine de la technologie du bâtiment. Vos responsabilités sont les suivantes:Organiser, planifier et contrôler toutes les activités liées à vos projets.Représenter notre entreprise auprès des clients et des partenaires.Diriger et motiver une équipe compétente de collaborateurs par projet au sein de C-tech.Assumer la responsabilité finale de vos projets en cours, tant sur le plan technique que financier.Assurer la livraison dans les délais de systèmes fiables, testés et de qualité prédéterminée, avec un déploiement optimal des ressources.Aborder et résoudre de manière décisive les défis techniques, organisationnels et commerciaux.Si vous êtes prêt à relever ce défi passionnant dans la région dynamique de Bruxelles, nous vous invitons à lire la suite et à découvrir comment vous pouvez contribuer à notre réussite dans le monde de la technologie du bâtiment.Ce que nous recherchonsDiplôme. Vous êtes titulaire d'un master ou d'un bachelor en électricité ou en électromécanique ou d'une expérience équivalente. Expérience. Vous avez au moins 5 ans d'expérience. Bonne connaissance du néerlandais et du français. L'anglais est un plus.Compétences non techniques. Vous êtes une personnalité orientée vers le client et assertive, dotée de solides compétences commerciales et sociales.Esprit d'équipe. Vous avez la qualité de motiver vos collègues et de travailler en équipe avec eux.Communication. Vous avez la capacité de communiquer vos idées, opinions et messages de manière claire, convaincante et structurée à différents acteurs.Capacité empathique. Vous êtes capable de vous mettre à la place des autres et de comprendre leurs perspectives et leurs sentiments.Flexibilité. Vous avez une grande capacité d'adaptation et vous êtes capable de réagir rapidement et de vous adapter à de nouvelles circonstances lorsqu'elles se présentent.Dynamisme. Vous avez une mentalité proactive de "faire en sorte que cela se réalise" et vous êtes infatigable. Vous êtes orienté(e) vers les objectifs et les résultats, et vous avez la capacité de rester calme dans des situations de stress.La joie. Vous prenez plaisir à votre travail et vous le transmettez à votre équipe et à vos collègues. Vous avez une attitude optimiste et vous êtes capable de voir des opportunités, même dans des situations difficiles.Si vous ne répondez pas entièrement à toutes les exigences requises, mais que vous avez néanmoins le sentiment fort d'être le candidat idéal pour ce poste, nous vous encourageons vivement à postuler. Chez nous, nous apprécions l'initiative et la pensée créative. Nous croyons que la diversité des parcours, des compétences et des perspectives enrichit notre équipe. Donc, si vous pensez pouvoir apporter une contribution précieuse, nous serions ravis d'avoir de vos nouvelles et d'explorer les possibilités.Ce que nous offronsPackage salarial compétitif. Nous offrons un package salarial compétitif comprenant de nombreux avantages tels qu'un ordinateur portable avec des logiciels professionnels, un téléphone portable, benefits@work, Buddyfit, etc.Flexibilité. Chez Cordeel Group, nous ne sommes pas une entreprise où l'on se contente de pointer à l'horloge. Ainsi, le travail à distance et les horaires flexibles sont tout à fait acceptables. Nous valorisons la possibilité de créer un équilibre entre travail et vie privée et comprenons que la flexibilité est importante pour le bien-être et la productivité de nos travailleurs.C-Academy. Chez Cordeel Group, nous attachons une grande importance à votre développement personnel. Ensemble, nous établirons un plan de développement et vous offrirons la possibilité de développer vos talents et de grandir ensemble.Rapidité. Cordeel Group est une équipe de professionnels intelligents, rapides et passionnés qui s'engagent à « Transforming the future as the fastest builder by focussing on innovation to create smart, energy-efficient and low-carbon solutions”. En faisant partie de notre équipe, vous montrez que vous êtes capable de jongler entre plusieurs tâches et de hiérarchiser de manière efficace et efficiente.Pas de micro-gestion. Chez Cordeel Group, vous êtes responsable de vos efforts - dès le premier jour, vous faites partie de l'équipe et nous avons confiance en votre capacité à assumer vos responsabilités. Une aide et un soutien seront disponibles lorsque demandés et nécessaires, mais vous avez toute la motivation et les opportunités pour avoir un réel impact.Opportunités de croissance uniques. Cordeel Group est un groupe de plus de 50 entreprises. Nous vous offrons un poste stimulant et enrichissant où vous avez la possibilité de grandir à la fois au sein de votre département et de l'ensemble de l'entreprise. Lors de l'ouverture d'un nouveau poste, nous donnons toujours la priorité aux talents internes au sein de notre entreprise.Innovation. Chez Cordeel Group, le développement durable est une façon de faire des affaires et pas seulement une tendance à la mode. Nous nous engageons activement à réduire les émissions de CO2 liées à nos activités et nous souscrivons aux objectifs de développement des Nations unies pour mettre en œuvre la durabilité dans la pratique.De nombreuses activités amusantes. Nous organisons des activités d'équipe géniales, des événements sociaux, des réunions et des événements de réseautage à l'échelle de l'entreprise de manière régulière.

Job Description Nous sommes à la recherche d'un(e) directeur(trice) du service juridique expérimenté(e) et passionné(e) pour rejoindre notre équipe et jouer un rôle crucial dans notre quête d'un avenir plus vert. Ce poste est situé au sein de notre équipe juridique hautement qualifiée et passionnée à Montréal, Québec. En tant que membre important de notre équipe dynamique, vous serez essentiel(le) dans la mise en place et l'expansion de nos opérations en Amérique du Nord, contribuant de manière significative à la création de l'une des premières usines de batteries à grande échelle en Amérique du Nord. Votre expertise et votre leadership seront déterminants dans la formation de cette entreprise révolutionnaire. À propos du posteDans ce rôle clé chez Northvolt Amérique du Nord, vous aurez l'occasion d'établir un cadre juridique robuste et efficace, essentiel pour l'expansion des opérations de Northvolt, non seulement au Canada, mais aussi aux États-Unis et sur d'autres marchés internationaux. Votre arrivée chez Northolt se produit à un moment critique, vous offrant une opportunité rare d'influencer considérablement la croissance à la fois d'une entreprise naissante et d'une industrie émergente. Vos responsabilités engloberont un large éventail de soutien juridique pour nos opérations canadiennes. Cela inclut la gestion des affaires corporatives générales, des accords de vente et de chaîne d'approvisionnement, du droit de la construction, des processus de financement, des problématiques juridiques liées aux RH, des questions de conformité, et de fournir des conseils juridiques continus pendant les phases de production du projet Northvolt à Montréal, Canada. À propos de l'équipeEn tant que principal(e) conseiller(ère) juridique de Northvolt au Canada, vous aurez la responsabilité unique de superviser tous les aspects juridiques de nos opérations canadiennes. En parallèle, vous serez un acteur clé au sein de notre équipe juridique mondiale en pleine expansion, qui compte plus de vingt professionnels expérimentés en Suède, en Pologne, en Allemagne, et désormais au Canada. Ce rôle offre l'opportunité excitante d'allier une expertise locale à une perspective globale. Principales responsabilités:Rédiger, examiner, négocier et conseiller sur les contrats et documents juridiques, en mettant particulièrement l'accent sur les accords de construction et de financement dans le cadre des opérations commerciales de l'entreprise. Fournir des conseils juridiques et des orientations à la direction sur diverses questions juridiques et politiques pertinentes pour l'activité de l'entreprise. Gérer et répondre aux affaires et litiges juridiques, en formulant des stratégies de résolution efficaces. Coordonner les relations avec le département juridique en Suède, ainsi qu'avec des experts juridiques et des avocats externes. Soutenir et améliorer les accords types, la gestion des contrats et les processus juridiques. Mettre en place des systèmes et procédures améliorés selon les besoins. --- DIRECTOR OF LEGAL AFFAIRS – NORTH AMERICAWe are looking for a seasoned Director of Legal Affairs to join our team and play a crucial role in our journey towards a greener future. This position is situated within our highly skilled and passionate legal team in Montreal, Quebec. As part of our dynamic team, you will be instrumental in setting up and expanding our North American operations, contributing significantly to creating one of the first large-scale battery factories in North America. Your expertise and leadership will be pivotal in shaping this groundbreaking venture. About the jobIn this pivotal role as part of Northvolt North America, you will have the chance to establish a robust and efficient legal framework, essential for scaling Northolt's operations not only in Canada but also in the U.S. and other international markets. Your arrival at Northolt comes at a critical juncture, offering you a rare opportunity to significantly influence the growth of both a nascent company and an emerging industry. Your responsibilities will encompass a broad spectrum of legal support for our Canadian operations. This includes managing general corporate affairs, sales and supply chain agreements, construction law, financing processes, HR-related legal issues, compliance matters, and offering continuous legal guidance during the production phases of the Northvolt project in Canada. About the teamAs Northolt's primary legal counsel in Canada, you will have the unique responsibility of overseeing all legal aspects of our Canadian operations. Simultaneously, you will be a key player in our growing global legal team, which boasts over twenty seasoned professionals across Sweden, Poland, Germany, and now including Canada. This role offers the exciting opportunity to blend local expertise with a global perspective. Key Responsibilities:Draft, review, negotiate, and advise on contracts and legal documents, especially focusing on construction and financing agreements within the company's business operations. Provide legal counsel and guidance to management on various legal and policy matters relevant to the company's business. Manage and respond to legal cases and disputes, formulating effective resolution strategies. Coordinate relations with the legal department in Sweden, as well as with external legal experts and lawyers.