Überblick über die Statistik des Gehaltsniveaus für "Specialist Computer System Compliance 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: LinkedIn Facebook Twitter Email

Junior Data Privacy Manager (m/f/d) Pierburg GmbH in Neuss Ref.-Nr.: DE09114 Schedule type: Full Time Contract Type: Permanent Position WHAT WE ARE LOOKING FOR Advising and informing companies and specialist departments in your area of responsibility on all data protection issues Implementing the data protection management system (DSMS) in close coordination with the Data Privacy Officer Support in ensuring operational standards for data protection and in implementing legal data protection requirements Regular reporting on the identification of data protection risks and implementation of data protection measures to the Data Privacy Officer Supporting the Data Privacy Officer Implementation of awareness measures, training courses and workshops Documentation of data protection incidents Supporting the specialist departments in guaranteeing the rights of data subjects Coordination of the (regional) data privacy managers and data protection contact persons in coordination with the Data Privacy Officer WHAT YOU SHOULD BRING WITH YOU Successfully completed studies in the fields of economics, law, business law, EU law, compliance, computer science or similar First professional experience in the field of data protection desirable Basic knowledge of topics such as information security / ISMS, DSMS and integrated management systems Solid IT knowledge and a strong understanding of IT topics (especially IT security) Business fluent in written and spoken German and English Quick comprehension and a good understanding of operational processes and structures in an international group Ability to communicate with target groups and a confident manner Solution-oriented and forward-looking way of working as well as the willingness to take on new topics WHAT WE OFFER YOU We offer you a creative, dynamic working environment in which you will play a central role as (Junior) Data Privacy Manager (m/f/d). We need your expertise to meet the ever-increasing demands in the areas of mobility and security. As an employee in our company, you will benefit from a positive working atmosphere in which you can feel comfortable in the long term. Together with your motivated colleagues, you will work with us on new, exciting and unusual technologies and products for global markets. At our location in Neuss we offer you Attractive remuneration Flexible working time models Fitness and health offers Corporate benefits platform A wide range of individual personnel development opportunities Your strengths and experience count at Rheinmetall. We also value diversity and equal opportunities. Applicants with severe disabilities will be given special consideration if they are equally qualified. We look forward to receiving your application. CONTACT DETAILS Ansprechpartner: Herr Felix Bloch Standort Pierburg GmbH, Neuss

Wir bei der TEXAID-Gruppe finden: Man lebt nur einmal – deshalb ist es so wichtig, Kleidungsstücken ein zweites Leben zu geben. Denn mit dem Recyceln gebrauchter Textilien machen wir Mode für alle Generationen bezahlbar. Und leisten einen wichtigen Beitrag zum Klimaschutz – für zukünftige Generationen unbezahlbar. In Zahlen heißt das: Seit über 40 Jahren sammeln, sortieren und verwerten wir gebrauchte Kleidungsstücke. Heute verarbeiten über 1.000 Mitarbeitende jährlich rund 80.000 Tonnen Alttextilien, unter anderem in einer der größten Sortieranlagen Deutschlands in Apolda. Zudem betreiben wir unter der Marke „ReSales“ die größte Secondhand-Filialkette Deutschlands mit mehr als 80 Shops. Möchtest auch Du in Deinem Arbeitsleben einen nachhaltigen Eindruck hinterlassen? Natürliche Ressourcen schonendes Textilrecycling nach außen tragen? Und Deinen Teil dazu beisteuern, dass der Klimaschutz noch mehr Fahrt aufnimmt? Dann beeindrucke uns nachhaltig mit Deiner Bewerbung und werde Teil von einem der führenden Textilrecycler Europas. Für unser Headquarter in Darmstadt suchen wir zum nächstmöglichen Zeitpunkt eine/nIT Specialist (m/w/d) POS SystemeDein Job:Du bist der Go-to-Guy (oder Girl) für den 1st und 2nd Level Support für unsere Kollegen in den Retail Stores.Unser Ticket System unterstützt Dich bei der Lösung der gestellten Anforderungen. Du bist der Held unseres User Helpdesk für unser Kassensystem.Du knackst Fehlercodes und behebst Probleme, sowohl mit unseren internen Teams als auch mit externen Dienstleistern.Du übernimmst die Rolle des Mastermind für die Beschaffung und des Rollouts des Kassensystems in ganz Deutschland und perspektivisch in Europa.Ebenso bist Du verantwortlich für die Mitgestaltung der internen Retail IT Prozesse.Deine Skills:Du hast eine abgeschlossene Ausbildung zum Fachinformatiker für Systemintegration oder eine vergleichbare Ausbildung. Alternativ verfügst Du über entsprechende Berufserfahrung in einem ähnlichen Aufgabengebiet.Du bist der Experte für Warenwirtschafts-, Zeiterfassungs- und Kassensysteme sowie Kassenhardware. Idealerweise hast Du Erfahrung in der Kassenführung.Deine Kunden- und Serviceorientierung ist on point. Du liebst es, Dienstleistungen zu erbringen.Du bist ein Schnelllerner mit hoher Lernbereitschaft.Deine sehr guten Deutschkenntnisse, sowie Dein gutes Englisch im Hinblick auf unsere zukünftige europaweite Expansion runden Dein Profil ab.Unsere Benefits:Über 40 Jahre Erfahrung in der nachhaltigen Weiterverwendung gebrauchter TextilienHochmotiviertes Team in einer lockeren und ungezwungenen ArbeitsatmosphäreSinnvolle Arbeit mit einem positiven Beitrag für unseren Planeten – Textilrecycling ist aktiver Klimaschutz​Die besten KollegInnen der Welt: über 1200 weltweit und über 900 deutschlandweit​20 % Zuschuss zur betrieblichen Altersvorsorge​20 % Rabatt in unseren über 80 Secondhand-Stores​ und Online ShopsInteressante Angebote über Corporate BenefitsKontakt:Du findest, dass eine textile Zukunft ohne Nachhaltigkeit Vergangenheit sein sollte? Und Du möchtest Deine diversen Fähigkeiten in einem diversen Umfeld einbringen? Dann überleg nicht lange und bewirb Dich mit einem Kurz-Lebenslauf. Platzangst? Keine Sorge: Solange die Stelle online ist, sind noch Plätze frei.Fragen? Dann „trage“ sie gerne an uns heran.Deine Ansprechpartnerin Nadine Schnell steht Dir gerne zur Verfügung.Über das Unternehmen:TEXAID Group

OverviewArcfield is a leading provider of full lifecycle, mission-focused systems engineering and integration capabilities to the U.S. government and its allies. The company has more than 60 years of proven experience providing advanced engineering and analysis, IT and C5ISR capabilities to support our nation’s most critical national security missions. Headquartered in Chantilly, VA and with 16 offices around the world, Arcfield employs approximately 1,200 engineers, analysts, IT specialists, and other professionals who put our customers’ missions first, helping them solve their most complex challenges through innovations in modeling, simulation and analysis, digital transformation and C5ISR. Visit arcfield.com for more details.ResponsibilitiesAs a Computer Forensic Scientist, you will support US Army Europe/Africa G2 and other Intelligence related mission partners, as a key team member of a complex program that provides professional services in support of advisory and analysis efforts associated with Intelligence Warfighting Function (IWfF)mission areas. The USAREUR-AF Team will research, analyze, and produce near- and long-term all source assessments on terrorism / counterterrorism, and multi-discipline counter-intelligence issues in response to CG USAREUR-AF’s priority intelligence requirements and to enable U.S. and foreign partner counterintelligence operations. You will be a member of a team that supports the Intelligence Directorate of the Army Component Command of both the US European Command and US Africa Command.You will embed in either Wiesbaden Germany OR Vicenza Italy and may travel within the theaters as required.Analyze digital forensic Tactics, Techniques, and Procedures (TTPs) related to the exploitation of digital media captured or seized in support of CI activities. Configure, update, and maintain forensic equipment and software. Prepare specialized technical products, including comprehensive documentation of network topology and information flow processes. Demonstrate a comprehensive understanding of Microsoft (MS) Active Directory, Hypervisors, virtual machines, databases, and Domain management.Exhibit a thorough understanding of Routers, Switches, cable management, and the ability to configure devices to effectively manage traffic flow.Accurately prepare and complete tasks and milestones associated with DoD System Security Plans for the assigned managed domain.Prepare specialized technical products, including comprehensive documentation of network topology and information flow processes.Ensure the configuration, update, and maintenance of forensic equipment and software in compliance with established policies.QualificationsRequired: BS 8-10, MS 6-8, PhD 3-5Must POSSESS and be able to maintain aTS/SCI clearance​Equal Pay ActThis is the projected compensation range for this position. There are differentiating factors that can impact a final salary/hourly rate, including, but not limited to, Contract Wage Determination, relevant work experience, skills and competencies that align to the specified role, geographic location (For Remote Opportunities), education and certifications as well as Federal Government Contract Labor categories. In addition, Arcfield invests in its employees beyond just compensation. Arcfield ’s benefits offerings include, dependent upon position, Health Insurance, Life Insurance, Paid Time Off, Holiday Pay, Short Term and Long-Term Disability, Retirement and Savings, Learning and Development opportunities, wellness programs as well as other optional benefit elections. Min: $92,109.68 Max: $221,338.19EEO StatementEEOArcfield proactively fulfills its role as an equal opportunity employer. We do not discriminate against any employee or applicant for employment because of race, color, sex, religion, age, sexual orientation, gender identity and expression, national origin, marital status, physical or mental disability, status as a Disabled Veteran, Recently Separated Veteran, Active-Duty Wartime or Campaign Badge Veteran, Armed Forces Services Medal, or any other characteristic protected by law. Standort Arcfield, Wiesbaden

Für unsere Abteilung Digital Products and Services – Engineering in Marburg suchen wir aktuell einenBusiness Systems Architect (m/w/x) / R-228696(Vollzeit / unbefristet / Level 7) Ausschreibungsende: 09.04.2024The OpportunityDrawing on your professional experience, you will specialize in understanding the business usage of information technology and allowing technology to contribute to the business. You will have a focus on contributing to the development of enterprise application standards, strategies and plans, and on eliciting requirements and delivering solutions according to identified needs in collaboration with different partners. Based on sound analysis, you will provide technical guidance and lead the technical implementation and support the adoption and ongoing use of application systems while following CSL governance standards. Also, You will contribute to the definition and maintenance of a functional, reliable, and cost-effective technology environment for the areas assigned and for identifying improvements. The colleague in this role will work unsupervised on projects and problems of complex scope and may coordinate the activities of others. May perform as a Developer using an approved software programming language to implement global IT strategy.The RoleAnalyze and Define RequirementsResponsible for the analysis and visualization of complex business processes. Accountable for the elicitation and evaluation of our requirements in collaboration with multiple stakeholders and translates these into functional requirements of the target solution. Establish scope and parameters of systems analysis to define outcome criteria and measure-taking actions. Lead a team using internal and external resources to deliver systems evaluations and solution design. May mentor other Analysts or Developers.Draft and DesigningAccountable and responsible for identifying the design and architecting or coding the target solution and preparing the required system design documentation (architectural specifications, diagrams and charts, functional and configuration specifications) to ensure the visualization of the technical implementation of user requirements, and to provide direction to system programmers. Collaborate with Infrastructure specialists and direct to deliver the target technology environment.Implement the design by means of configuration and software development using internal and external resources. May mentor other Analysts or Developers and perform peer reviews of design solutions or coding to further develop standards.Test and ValidationCompile validation planning in agreement with a Quality position. Manage the implementation of the defined measures in the validation plan. Prepare test cases and coordinates test reports in collaboration with other departments observing CSL defined quality and governance standards and procedures. Collaborate with Process Owners/Business stakeholders to ensure test applicability. Conduct system functional testing with internal or external resources. Contribute to the identification of enterprise standard approaches to testing and validation applicable to the CSL framework.TrainingPrepare training materials and user manuals. Design and conduct user training sessions, with emphasis on relating the configuration and technical setup to the business requirements and defined CSL enterprise application standards. Help identify enterprise standard approaches to Training as applicable to the CSL framework.Operations and SupportAccountable for the ongoing operation and maintenance of applications for the assigned IT areas, including the definition and monitoring of the measures to ensure system availability. Accountable for the provision of 2nd or 3rd level incident support, change management, and maintaining the upkeep of technical records and documentation. Communicate the status of ongoing daily support and problem resolution. Ensure problem investigations and resolution of issues of complex scope and escalate issues when needed to appropriate levels of IT or Business. May provide off hours support as it relates to the IT functional area.Project WorkDefine or lead a project team for complex, business critical projects. Perform matrix roles as assigned for local and global projects in areas within and outside core area of proficiency. Define scope, plans, and manages projects involving the technical solution including data sourcing, migration, design, implementation, and quality assurance.Teamwork and LeadershipLead by example in working collaboratively with internal employees, vendors, and consultants to implement solutions. Develop mutually productive relationships in the workplace. Use a network of main contacts within and outside the Technology area for the benefit of the team.May contribute to the definition and planning of team targets and strategy and coordinate the activities of others to deliver these. May contribute to departmental budget and resource planning.InnovationDirect and conduct research and evaluation on new solutions, releases, enhancements and considers their applicability to CSL.Lead the identification and implementation of means to improve the qualities and efficiencies of IT processes, systems, and results. Keep informed about current technologies, associated strategies and professional concepts as it relates to the assigned IT functional area.Maintain Regulatory ComplianceFollow global IT procedures and policies as defined by our Quality Management System (QMS). Follow the appropriate global regulatory guidelines and current Good Manufacturing Practice (cGMP).StrategicContribute to the development of enterprise-wide technical strategies, designs, and plan that support Business strategies and the development of the Application Portfolio. Work constructively to support changes to policies, procedures and standards relating to the enterprise application landscape. May define or manage coding standards for Development. Manage relationships with Application vendors according to CSL stakeholders.Enterprise ArchitectureAccountable to Enterprise Architecture for conformance and alignment to EA enterprise-wide systems strategies and standards relating to the enterprise application landscape. Participate in the EA System Architect (EASA) Forum.Your Skills and ExperienceBachelor’s degree or equivalent experience; educational concentration in a computer-based discipline (e.g., Computer Science, Information Systems) or a technical discipline (e.g., Engineering, Mathematics) is preferred.Master’s Degree is preferred.8+ years of experience in IT working within an applicable function that directly aligns with the responsibilities for this position.Pharma/Biotech or similarly regulated environment experience preferred.Work with Microsoft Office products, such as Project, PowerPoint, SharePoint, Excel, and Visio.Knowledgeable working in the Systems Development Life Cycle (SDLC).Ability to develop others on business process, and knowledge across several departments.Business Systems Analyst & Solution Architect related Functional/Technical Skills.Preferred Technologies:JavaJavaScriptOracle PL SQLPostgreSQLApp & Web Development in generalOur BenefitsWe encourage you to make your well-being a priority. It’s important and so are you. Learn more about how we care at CSL.About CSL BehringCSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas. Learn more about CSL Behring.We want CSL to reflect the world around usAs a global organisation with employees in 35+ countries, CSL embraces diversity and inclusion. Learn more about Diversity & Inclusion at CSL.Do work that matters at CSL Behring!

Job Description As a Business Analyst in the Life Sciences/Healthcare industry, you will play a vital role in bridging the gap between business needs and technology solutions. You will closely interact with diverse and both internal and external stakeholders including IT teams, Business, Functions and Healthcare professionals. Your primary responsibility will be to understand and analyse the organization's business, processes, workflows, needs and translate them into quality requirements and other artifacts.Key Responsibilities:Requirements Elicitation, Analysis and Documentation:Follow elicitation techniques such as conduct interviews, workshops to understand and confirm end-user needs.Collaborate with stakeholders to analyse and document business requirements in the form of specifications, use cases, user stories, mock-ups.Process Analysis and Mapping:Analyse existing healthcare processes and workflows to identify opportunities for optimization and automation.Create process maps, flowcharts, and business process models to visualize current and future states.Solution Design:Work closely with IT teams and vendors to design technology solutions that align with business requirements.Evaluate and recommend software applications, systems, tools or processes that address specific healthcare challenges.Data Analysis and Reporting:Possess basic knowledge to analyse data and derive meaningful insights to - solve a problem, find root cause, implement improvements.Develop and maintain reports and dashboards to monitor key performance indicators (KPIs) and support data-driven decision-making.Regulatory & Compliance:Stay abreast with healthcare regulations, industry standards, and best practices (e.g., HIPAA, HL7, CFR Part 11, SOX, HIPAA, CSV, GxP, GDPR) to ensure that technology solutions comply with relevant guidelines.Change Management and User Training:Assist in change management efforts by preparing training materials, conducting user training sessions, and supporting end-users during technology adoption.Project Management Support:Collaborate with project managers to define project scope, objectives, and deliverables.Monitor project progress, identify risks, and help resolve issues to ensure successful project completion.Quality Assurance and Testing:Support testing efforts by defining test protocols, test cases, conducting user acceptance testing (UAT), and validating that solutions meet business requirements.Qualifications:Bachelor/Master’s degree in Computer Science, Business Administration, BioChemical, BioMedical, BioInformatics,...Proven experience as a Business Analyst in the healthcare industry. IStrong understanding of healthcare processes, clinical workflows, and terminology.Knowledge of healthcare regulations and compliance requirements (e.g. HIPAA, Meaningful Use).Familiarity with healthcare IT systems, EHRs, and other healthcare applications such as LIMS, CTMS, ERP, CRM, Supply Chain Management systems.Excellent analytical, problem-solving, and communication skills.Proficiency in data analysis and reporting tools.Ability to work effectively in cross-functional teams and communicate complex technical concepts to non-technical stakeholders.Certification in Business Analysis (IREB, CCBA, CBAP)Hard Skills:Able to use Business Analysis techniques and tools in analysis.Familiar with Agile and Waterfall methodologiesExperience with BPMN, UML is an add-onExperience (set-up & use) with tools like Confluence & JIRAExperience (use) with tools like, Visio & TableauExperience with creating wireframes, mock-upsExperience in writing Epics, Features, User Stories or Use CasesSoft skills:Strong communication skills (written and verbal)Communicate proactively. Ability to communicate effectively with stakeholders. Engage with people from different functions.Multi-tasking skills. Ability to work on multiple projects or tasks simultaneouslyOwnership of workWork autonomously and be a value-adding team-playerEntrepreneurship mindedStrong analytical and research skillsNice to have:PhD or equivalent degree in BioChemical, BioMedical, BioInformatics or related field.Knowledge/Experience in ERP (Eg: SAP), CRM (Eg: Salesforce), SQL, Analytics, Web & Mobile applications, Hospital integrations(HL7)Certifications: Scrum Product Owner, SAFe, ITILLanguage and Location:Resident in Belgium or open to relocateFluent oral and written communication skills in English and at least understand and speak French and/or DutchWilling to travel occasionallyWhat we offer:You’ll be joining a great team of people who are passionate about their job. You will be given a lot of trust and freedom. You will learn a lot of new things and will be able to take on new challenges. We also value your personal growth and private life. A lot of flexibility will be provided.We promote a culture of diversity. We believe working with talented individuals from different backgrounds and points of view is a strategic advantage and an ongoing opportunity. Diversity enriches our creative solutions and adds value for our clients.With the digital tech sector growing at a rapid pace and women significantly underrepresented in the industry, we are determined to inspire and recruit more women into technology and build diverse teams that reflect the clients we serve.In exchange for your work and commitment, you will be rewarded with a nice salary, a shiny company car, fuel card, lunch vouchers, eco-cheques, flexible hours, 32 vacation days, a flex plan, a mobility plan, a share ownership plan, hybrid working and so much more.

Job Description Open Application for Future Opportunities:Are you eager to be part of a pioneering initiative in the sustainable energy sector? Northvolt is actively seeking exceptional individuals to join our dynamic Blueprint Team. While specific roles may not be available immediately, we encourage passionate individuals with expertise in various fields to submit their profiles for consideration. We are building a talent pool to draw from as opportunities arise within the Blueprint Team.About the Blueprint Team:The Blueprint Team is on a mission to develop a digital factory blueprint for a scalable, rapidly deployable, highly efficient world-class battery factory. It constitutes a complete solution that spans process, equipment, materials, facility, utilities and people, with guidelines and tools needed for the establishment of a factory.Factory Integration, CSA and MEPIn Factory Design team, especially in CSA & Factory Integration team and MEP & Energy team, we care about the holistic design of the factory. The team is responsible for the creation of standards and guidelines with the main purpose of designing an optimized architectural shell which allows the performance of the whole battery manufacturing process, as the same time we coordinate, assess, and develop during the preliminary stages of the project. *(Senior) Architectural Design Engineer: Key responsibilities included but not limited to:Creation and review of Northvolt architectural design philosophies and guidelines.Collect, coordinate and structure the architectural design requirements from the factory users, amongst all teams and engineering disciplines while ensuring coordination between internal/external stakeholders and design consultants and compliance with environmental requirements.Preparation and review of concept and basic design and provide technical support during Detail Design and Execution phases, acting as the main design authority.The person we are looking for has experience in construction is flexible, curios and eager to learn. You will get the chance to have a real impact on our success story in Sweden (to start with) and see the results of your work. Our organization values great self-discipline and a natural talent to make things happen. Qualities that we cherish are sense of quality, friendliness, grit and a sense of humour.****We believe that you have : Bachelors or Master’s in Architectural Engineering10+ years working experience, preferably in industrial projectsExcellent English written and oral skillsProficiency in 2D/3D software, such as Auto CAD, Revit, 3d Studio MAX, Illustrator, Photoshop, InDesign and/or SketchUpBonus points for: Experience and interest in manufacturing industryFluency in other languages (Swedish, German)Previous experience with large scale projects is strongly desirable but not essential(Senior) Structural Design EngineerKey responsibilities included but not limited to:Creation and review of Northvolt structural design philosophies and guidelines.Collect, coordinate and structure the structural design requirements from the factory users, amongst all teams and engineering disciplines.Ensure coordination between internal/external stakeholders and design consultants and compliance with environmental requirements.Preparation and review of concept and basic design within the Structural discipline.We believe that you have:Bachelors’ Degree in Civil or/and Structural Engineering10+ years working experience, preferably in industrial projectsExcellent English written and oral skillsStrong experience with both 3D and 2D design tools such as Revit Structural, as well as Robot and/or Staad ProBonus points for: Experience and interest in manufacturing industryFluency in other languages (Swedish, German)Previous experience with large scale projects is strongly desirable but not essential(Senior) Civil Design Engineer Key responsibilities included but not limited to: Preparation and review of concept and basic design within the Civil discipline.Provide technical support during Detail Design and Execution phases, acting as the main design authority..Develop and review civil engineering deliverables, including construction document drawings, specifications, and calculations (i.e. roads, grading, drainage, deep piping, layout and design geometric, paving, and site utilities, etc.)We believe that you have: Bachelors’ Degree in Civil Engineering+10 years’ work experience in building industry, preferably designing complex manufacturing/production facilities and its infrastructureStrong experience with Revit, AutoDesk Civil 3D for civil site design or VestraGreat English written and oral skills to ensure smooth and efficient communicationBonus points for: Previous experience with large scale projects is strongly desirable but not essentialFamiliarity with Swedish and European laws and standardsDesign Manager - Building Integration Key responsibilities included but not limited to:Drive and manage, together with a cross-functional team within Northvolt, the design of a key building block in our factory blueprint.Set the direction and drive technical decisions on the design to ensure that the factory designs are competitive (cost/performance), modular, easy to ramp up, and possible to operate in a sustainable way.Organize and manage design reviews, construction design packages and deliverables to support all aspects of construction, including scope of work, kick-off, studies, 30-70-90, etc.We believe that you have: Bachelors’ Degree in Architectural (preferred), civil, mechanical, structural or equivalent.10+ years working experience, preferably coordinating cross-functional teams and managing resources.Excellent English written and oral skills.Experience driving complex industrial projects and broad understanding of engineering disciplines.Bonus points for:Proficient in MS Suite.Fluency in other languages (Swedish, German).Experience in multi-cultural environments.Ability to work under high pressure and tight deadlines Design Manager - Site Integration Key responsibilities included but not limited to: Drive and manage, together with a cross-functional team within Northvolt, the design of a masterplan in our factory blueprint.Set the direction and drive technical decisions on the design to ensure that the factory site designs are competitive (cost/performance), modular, easy to ramp up, and possible to operate in a sustainable way.Organize and manage design reviews, construction design packages and deliverables to support all aspects of construction, including scope of work, kick-off, studies, 30-60-90, etc.We believe that you have: Bachelors’ Degree in Architectural, civil, electrical, mechanical, structural or equivalent.10+ years working experience, preferably coordinating cross-functional teams and managing resources.Excellent English written and oral skills.Experience driving complex industrial projects and broad understanding of engineering disciplines.Bonus points for: Proficient in MS Suite.Fluency in other languages (Swedish, German).Experience in multi-cultural environments.Ability to work under high pressure and tight deadlines Global Discipline Lead C&D RoomKey responsibilities included but not limited to:Creation and review of Northvolt Clean and Dry Room design philosophies and guidelines, as collecting, coordinating and structuring the Clean and Dry Room design requirements from the factory users, amongst all the teams and engineering disciplines.Make technical decisions for competitive, modular, scalable, and sustainable designs. This includes facilitating design reviews, managing blueprint upgrades, and reporting results to management.Capture Lessons Learned, establish and drive standards for key design documents, and co-develop/collect design documents such as Technical Equipment Specifications and User Requirement Specifications.We would like to include a proactive, innovative, and curious person who can bring and assess new solutions for C&D room, with solid experience in this environment and with construction experience We believe that you have:Bachelor's Degree in Mechanical or/and Industrial Engineering or equivalentMinimum of 10 years of experience preferably in industrial projects, especially in the Clean and Dry Room scope (Battery Knowledge is a plus)Strong experience with both 3D and 2D design tools such as Revit or AutocadBonus points for:Proficient in MS Suite.Fluency in other languages (Swedish, German).Experience in multi-cultural environments.Ability to work under high pressure and tight deadlinesGlobal Discipline Lead - Electrical + I&C Engineer Key responsibilities included but not limited to: Creation and review of Northvolt Electrical + I&C (EIC) design philosophies and guidelines.Collect, coordinate and structure the EIC design requirements from the factory users, amongst all teams and engineering disciplines.Ensure coordination between internal/external stakeholders and design consultants and compliance with environmental requirements.Preparation and review of concept and basic design within the EIC disciplines.We believe that you have: Bachelors’ Degree or Masters’ in Electrical Engineering or equivalent.10+ years working experience, preferably in industrial projects (such as pharma, data centers, oil & gas, automotive), especially in the EIC scope.Experience with design and/or commissioning in the field of HV, MV, LV and associated control and protection system.Excellent English written and oral skills.Bonus points for: Proficient in MS Suite.Experience with CAD software (AutoCAD…) for electrical and control systems is preferred but not required.Fluency in other languages (Swedish, German).Experience in multi-cultural environments.Ability to work under high pressure and tight deadlines.Familiarity with Swedish and European laws and standardsKnowledge of Instrument & Control (I&C) or Building Monitoring System (BMS) design techniques, tools, and principals involved in production of requirements and concept design deliverables.Electrical Engineer Specialist - Power System CalculationKey responsibilities included but not limited to: Modelling under the ETAP software the internal electrical distribution networks to carry out the electrical studies associated with a project as well as the corresponding calculation notes,Power system calculations and associated reports: load distribution and voltage profile, short-circuit, motor starting, cable calculations, harmonics, dynamic studies, arc flash, discrimination and protection settings,Development and/or validation of the HTB-HTA-LV protection schemes implemented throughout our distribution systems,Analyse the requirements of the system operator (Grid Code) to carry out HTB / HTA connection studies and coordinate the technical requirements with the Electrical Design ManagersWe believe that you have: Bachelors or Master’s in Electrical engineeringMinimum of 4 years experience in electrical design/engineering for heavy industrial, manufacturing or process facilities such as pharmaceutical, data centres, oil & gas, automotive, food & beverage manufacturing, etc.Good theoretical basis for electrical calculations (sizing of cables, transformers, PFC, motor starting, load studies, load flows, short circuit calculations, harmonic studies and earth grid designs)Preference if prior minimum experience using power systems simulation software such as ETAP, Powerfactory, MATLAB power system toolbox etc.Fluency in English. Valuable (but not required) if fluency in other languagesComputer literacy (Word, PowerPoint, Excel, Project)