Überblick über die Statistik des Gehaltsniveaus für "Project Chemist 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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Job Description About the jobThe key responsibilities of the Testing manager is to plan, manage and coordinate the daily activities of a sub-team within the Laboratories Quality team at Northvolt ETT. This includes ensuring the execution of the control plan, both the logistics and successful testing of cells, as well as collaborating with stakeholders from production/quality/logistics/R&D/cell design to support them as best as possible in terms of their daily testing needs and requirements. Additionally, the Testing Manager’s responsibility is to maximise the use of available resources (personnel, equipment, material), build a strong and talented team that can meet the high demands of our internal customers in terms of quality, efficiency, and turn-around time of results. Key responsibilities include but are not limited to:The Quality Control Area Manager has several key types of responsibilities, each with a distinct set of duties and expectations. In addition, this role requires a high degree of flexibility and ability to cope with ambiguity and rapid change in production operations and quality control needs. The main types of responsibilities and expectations thereof are (in no particular order of priority): Direct Management of Employees. This role usually has several direct reports and as such the Area Manager is expected to handle the day-to-day management of these employees, including: Assistance with hiring and onboarding. Attendance. Vacation, holiday, and other time-off management and approvals. Corrective actions for behaviour if required. Ensuring all basic company compliance type training (e.g., safety, company policy) is attended and adhered to. Operations Management of specific QC activities (both employees and throughput). This responsibility is concerned with the actual productivity of the sub-team. Management of the execution of all quality control analyses of the sub-team as per the control plan. Plan and communicate to the team their daily/weekly priorities (immediate to 168-hour timeframe), ensure expectations and responsibilities are clear. Responsible for short-term planning and scheduling of people and resources to achieve optimal throughput, as well as any necessary planning involved with control plan and project changes. Coordinate logistics of incoming/outgoing samples to/from QC lab; immediate collection and reporting of results back to production. Support the team with running analytical testing on a range of instruments. Ensure non-conformities about material deviations are reported and follow up on improvement. Operational Training, Quality, and Safety Compliance of Direct Personnel and Daily Processes. The Area Managers are responsible for ensuring that basic expectations and requirements are met, which includes: Strict adherence to all safety requirements and safe operation/handling of equipment and materials by all team members. ensure the team works in the safest manner possible. Drive continuous improvement of ways of workings and analyses to increase the team’s efficiency and optimize analyses turn-around times. Ensure continuous cross-training within the team; set up training sessions, develop & grow expertise within the team for them to be able to safely and competently perform their tasks. Ensure SOPs and WIs are being followed and continuously updated. This includes strict adherence to Northvolt’s 5S standards. Expect, Plan For, and Manage a Certain Degree of Ambiguity and Constant Change. This job, due to the company still being a start-up environment, requires flexibility and the ability to work well and coordinate with others. It requires the ability to build relationships and trust across boundaries of responsibility, continuously collaborate with all internal customers to ensure to support them as best as needed, so that ultimately the company can operate as a team with a common goal, while still holding each other accountable for their respective expectations.Accountability/AuthorizationBudget responsibility: YesDirect reports: YesAuthorized to decide on investments according to role and policy.The person we are looking for is driven, caring and structured. You thrive by leading others and work towards common goals. You are used to a high paced work environment and got good time management skills. Qualities that we cherish are flexibility, sense of quality, friendliness, motivation to take on new challenges, grit and a sense of humor. Northvolt is an equal opportunity employer. We're a diverse group of individuals, united by a common mission, who recognise that while our actions as individuals have a role to play in driving Northvolt towards its goals, we always seek to move forward as a team. We offer you an open and welcoming atmosphere where we win as a team – and fail as a team. Northvolt is growing at the speed of light and we are a strong believer in internal career development. For us it’s important to look at your skills and potential, please refrain form including your picture and age with your application to help us with this. Apply with CV in english or your complete LinkedIn profile. Full time employment, fixed salary. Planned starting date is asap. Please note that any applications submitted via email or direct messaging will not be considered.

adesta - success is our attitude adesta sees itself as a partner for customers as well as for employees and applicants. Each appreciate the high-quality, individual advice and support which they receive at adesta. On behalf of our client, a world-renowned pharmaceutical enterprise with headquarters in the Rhine Main area, we are looking for aInterim Labeling Manager (m/f/d) in Rhein-Main-GebietYour tasksCreates and maintain Global Regulatory Product Information (Reference Product Information, RPI) documents as the basis for worldwide harmonized Labeling Leads all labeling-related activities within the cross functional product teams (e.g. Regulatory Sub-Team, Labeling Team, Global Project Team) for assigned products Ensures consistency between the RPI and national labeling documents and provide labeling related advise to the cross functional experts and to countries Coordinates and prepares response to labeling-related questions from authorities (content and format) Oversees creation and maintenance of minimum text requirements for global Master Packaging as the basis for worldwide harmonized packaging material Analyses competitor labeling Be aware of local and regional labeling requirements, particularly EU Provides revised SmPC, labelling and PL texts in English for EU procedures ( CP, MRP, DCP) Coordinate translations for CPs Have a solid knowledge on Pharmacovigilance requirements Working place: 80% on site, 20% remote Your ProfilePharmacist, chemist, biologist (f/m/d) or similar background At least 5 years regulatory and labeling experience in Pharma Industry Solid problem solving skills Excellent communication skills Fluency in English (oral and written) Are you interested in this challenging freelance job? Then please submit your profile (in English) under specification of reference number 29-302-244. If you have any questions, please do not hesitate to contact Mr. Jungclaus. Application Form Title*Please chooseMrs.Mr.Dr. First name* Surname* Street and number* ZIP* City/Town* Telephone number* E-Mail* Link to profile (ex. LinkedIn, Xing, Website, etc.) Your message Resume* Further attachments Attachment Attachment Attachment Maximum file size of all attachments is 10MB. How did you find us?*Please chooseadesta websiteBingBundesagentur für ArbeitFacebookGoogleindeedInitiativeInstagramLetter box advertisingLinkedInMonsterRecommendationjobvectorStellenmarkt.deStellenportal.deStepstoneTwitterXingOther Other Recommendation Declaration of Consent for the use of personal dataWe attach great importance to the highest possible protection of your personal data. The personal data are therefore protected by technical and organisational measures against unauthorised access and manipulations. The controller in accordance with data protection law isadesta GmbH & Co. KGWilhelminenstraße 2564283 DarmstadtTel.: +49 (0)6151 604070Fax: +49 (0)6151 6040777e-mail: [email protected] Consulting GmbHWilhelminenstraße 2564283 DarmstadtTel.: +49 (0)6151 604070Fax: +49 (0)6151 6040777e-mail: [email protected] Data Protection Officer isMr. Matthias StierWilhelminenstraße 2564283 DarmstadtTel.: +49 (0)6151 604070E-Mail: [email protected] contact our Data Protection Officer (see above) if you have any questions in connection with data protection and the storage and processing of your data. Our applicant management system and your dataadesta uses a database-supported applicant management system. The information and personal data provided by you within the framework of our applicant management system are compared with the requirements of the requested position and are used to offer you suitable jobs at potential employers.The data and information which we collect within the framework of the applicant management system include the data entered by you in the system, e.g.Name,Gender,Home address,Telephone number(s),e-mail address,Age,as well as any documents provided by you, e.g. Curriculum vitae, , Certificates/qualifications, Images/photographs and any data and information recorded during the application procedure, e.g. Contents of telephone interviews or video interviews,Contents of personal consultations,Contents of the applicant questionnaire,Recruitment tests.Collection, storage, processing, use and transfer of personal data to third partiesIf you send an application via our application management system, the data which you provide and all data and personal information collected during the application procedure will be stored - permanently by adesta - until we receive instructions to the contrary from you - and may be processed accordingly, used to perform a contract and also transmitted in this respect to our customers for the purpose of helping to find job placements/tasks. Your data are collected, processed and used in accordance with Article 6 (1) a) of the General Data Protection Regulation (GDPR)Purpose of processingYour data are collected, stored, processed and used for the purpose of offering you suitable jobs based on your profile and your placement requirements at potential employers, i.e. customers of adesta - now and in the future - and informing you accordingly about job vacancies. Einwilligung* Hiermit erkläre ich ausdrücklich meine Einwilligung, dass meine persönlichen Daten im Rahmen des zuvor beschriebenen Zwecks dauerhaft - d.h. bis zum Erhalt einer gegenteiligen Weisung von mir - von adesta in das elektronische Bewerber-Managementsystem aufgenommen, gespeichert, verarbeitet und genutzt und in diesem Zusammenhang entsprechend an potentielle Arbeitgeber, d.h. Kunden von adesta, weitergegeben werden können und adesta insoweit mich auch in Zukunft gemäß meines Anforderungsprofils über passende Stellenangebote informieren kann. Ich erkläre gleichzeitig, dass ich diese Einwilligung freiwillig abgebe.Gleichzeitig bestätige ich, dass ich den Fragebogen im Rahmen des Bewerber-Managementsystems von adesta wahrheitsgemäß ausgefüllt habe und dass die von mir zur Verfügung gestellten Unterlagen (z.B. Bilder, Fotografien) keine Rechte Dritter (wie z.B. Urheberrecht) verletzen.Your rightsRevocationYou may freely revoke your consent at any time with effect for the future and without specifying reasons by simply sending a declaration to adesta adesta GmbH & Co. KG Wilhelminenstraße 25 64283 Darmstadt Tel: +40 (0)6151 604070 Fax: +49 (0)6151 6040777 e-mail: [email protected] Consulting GmbH Wilhelminenstraße 25 64283 Darmstadt Tel: +49 (0)6151 604070 Fax: +49 (0)6151 6040777 e-mail: [email protected] effect for the future. In this context, we would like to point out that a revocation declared by you does not change the legality of the processing carried out until the revocation.Beyond that you have a right onInformation on the personal data concerned,Deletion of your data,Blocking or restricting your data,Correction of your dataReceipt of a free copy of your data data transferabilityIn such cases, please also contact our data protection officer at the aforementioned address or the appropriate contact options.Complaint to the supervisory authorityWithout prejudice to any other administrative or judicial remedy, you shall have the right to complain to a supervisory authority, in particular in the Member State of your residence, place of work or place of presumed infringement, if you consider that the processing of your personal data is in breach of the DSGVO.The supervisory authority with which the complaint was lodged shall inform the complainant of the status and outcome of the complaint, including the possibility of a judicial remedy under Article 78 DSGVO.Hinweis: Bitte füllen Sie alle Felder mit * gekennzeichnet aus.Don't fill this field!

Job Description Coordonnateur Assurance Qualité et du Contrôle QualitéNous recherchons un Coordonnateur Assurance et Contrôle Qualité (QA/QC) expérimenté pour nous rejoindre dans notre mission de contribuer à un avenir plus vert. Le poste fait partie de notre passionnante équipe de Construction basée au Québec. En nous rejoignant, vous jouerez un rôle clé dans l'établissement et le développement de l'une des premières usines de batteries d'Amérique du Nord à grande échelle.À propos du posteVous travaillerez en collaboration avec l'équipe de gestion de la construction et vous rapporterez au Gestionnaire Assurance Qualité et du Contrôle Qualité . Vous serez responsable de maintenir les plus hauts niveaux de qualité et de conformité tout au long de la phase de construction. Vous vous assurerez que toute la documentation qualité requise est préparée pour toutes les phases, jusqu’à la mise en service. Les plans de construction actuels sont une première étape pour la construction d'un grand campus industriel composé de diverses usines au cours des 5 à 7 prochaines années, avec des opportunités de développement de carrière dans la construction industrielle.À propos de l'équipeNotre équipe de Construction chez Northvolt est un groupe dynamique et dévoué de professionnels engagés à transformer les concepts visionnaires en réalité. Avec une expertise couvrant l'ingénierie, la gestion de projet, la sécurité qualité et la durabilité, nous sommes à l'avant-garde de la construction de gigafactories pour la production de batteries avancées. L'équipe sera basée sur le site près de Saint-Basile-le-Grand et de McMasterville.Les principales responsabilités sont : Développement de Processus : Surveiller la qualité de la construction et les processus de vérification conformément aux documents contractuels. Entreprendre et rendre compte des audits conformément au calendrier établit. Examiner les mesures correctives prises à la suite des non-conformités et des constatations d'audit Inspection et Tests : S'assurer que les entrepreneurs de construction et de mise en œuvre suivent les procédures QA/QC convenues et prennent des mesures correctives pour maintenir les plus hauts niveaux de qualité et de sécurité. Assister et libérer les inspections des points de d’arrêts et de témoignages déterminés. Collaboration : Collaborer avec les chefs de projet, les équipes d'ingénierie et les sous-traitants pour résoudre les problèmes de qualité, et soutenir les efforts d'amélioration continue tout au long de la construction. Participer aux réunions pour discuter des performances qualité et résoudre les problèmes de qualité. Rapports Qualité : Fournir régulièrement des rapports de qualité et des mises à jour aux parties prenantes du projet, mettant en évidence les domaines d'excellence, identifiant les opportunités d'amélioration et assurer la transparence des activités de contrôle qualité.Northvolt est un employeur qui respecte l'égalité des chances; nous sommes un groupe d’individus diversifié, unis par une mission commune. Puisque nous sommes en phase d’expansion ultra rapide, nous offrons des opportunités de développement professionnel et d’apprentissage continu à l’interne.Veuillez s’il vous plaît postuler avec votre CV ou profil LinkedIn. -----------------------------------------------------------------------------------------------Quality Assurance & Quality Control Coordinator ConstructionWe are looking for an experienced Quality Assurance & Quality Control (QA / QC) Coordinator to join us in our mission to contribute to a greener future. The role is a part of our passionate Construction team based in Quebec. By joining us, you will be a key player in establishing/ramping up our battery factory and contribute to building one of the first large scale North American battery factories. About the jobYou will be working closely with the construction management team and will report directly to the QA/QC Manager. Your role will involve co-ordination and control with the construction and installation contractors and collaborating with cross-functional teams to uphold the highest levels of quality and compliance throughout the construction phase. You will make sure that all required Quality documentation is prepared and ensure a smooth transition from the construction phase to the commissioning phase. The current construction plans are a first step for the construction of a large industrial campus consisting of various factories over the next 5-7 years with opportunities to grow your career in industrial construction. About the teamOur Construction team at Northvolt is a dynamic and dedicated group of professionals committed to turning visionary concepts into reality. With expertise spanning engineering, project management, Quality safety, and sustainability, we are at the forefront of building state-of-the-art gigafactories for advanced battery production. The team will be based on-site, close to Saint-Basile-le-Grand, and McMasterville. Key responsibilities include but are not limited to:Process Development : Monitor the construction quality and verification processes in accordance with the contract documents. Undertake and report audits in accordance with the audit schedule. Review corrective action taken as a result of non-conformance and audit findings. Inspection and Testing : Assure that the Construction and implementation contractors follow the agreed QA/QC procedures and taking corrective actions to maintain the highest levels of quality and safety. Attend and release Hold and Witness Point inspections. Cross-functional Collaboration : Collaborate closely with project managers, engineering teams, and subcontractors to address quality issues, provide guidance, and support continuous improvement efforts throughout the gigafactory construction. Participate in meetings to discuss quality performance and resolve quality issues. Quality Reporting : Provide regular quality reports and updates to project stakeholders, highlighting areas of excellence, identifying improvement opportunities, and ensuring transparency in quality control activities to uphold Northvolt's commitment to excellence in sustainable energy solutions.Northvolt is an equal opportunity employer. We're a diverse group of individuals, united by a common mission, who recognize that while our actions as individuals have a role to play in driving Northvolt towards its goals, we always seek to move forward as a team. We offer you an open and welcoming atmosphere where we win as a team – and fail as a team. Northvolt is growing at the speed of light and we are a strong believer in internal career development. Apply with your CV or LinkedIn profile.

Job Description We are looking for an experienced Senior Manager of our Cell Analysis Laboratory to join us in our mission to contribute to a greener future. The role is a part of the Quality Organisation, and integrated in Labs, our R&D centre in Västerås, where we are developing the next generation of battery technology. Here we produce, advance and validate materials and cells for our customers. By joining us, you will be a key player in understanding our battery cells and their components and contribute to building one of the first large scale European battery factories. About the jobChemical, physical and mechanical analysis are fundamental to understand our battery cells and their components, to select suppliers, to control quality of incoming material and in production, and to understand failure mechanisms and causes. In this role you manage and lead the Cell Analysis Laboratory, comprising a mechanical, a chemical and a failure analysis laboratory. You work with internal customers and equipment suppliers, define, own and execute the method and equipment roadmap, as well as the development and validation of analytical methods. Key responsibilities include but are not limited to:Responsible for operating the Cell Analysis Laboratory, including mechanical and chemical materials analysis, incoming quality control, process quality control and failure analysis.Leading and Managing a diverse organisation of e.g. Managers, Engineers, Analytical chemists, Metallurgists, Technicians and support functions.Identify and align analysis requirements from internal customers. Derive a methodology and -equipment roadmap, align with relevant stakeholders such as internal customers, experts and other laboratories, and execute it.Accountable for method development and -validation, as well as maintenance and calibration of the instruments, documentation and training.Accountable for the Cell Analysis Laboratory facilities, ensuring safe operation by employees in the laboratories at all times.Manage the project plan for establishment of the QC- lab including layout, specifications, support in the RFQ process and execution of installations and commissioning of new analytical instruments.Responsible for efficient execution of quality controls and inspections according to all control plans, demand vs capacity tracking, data management and storageThe person we are looking for is driven, caring and structured. You thrive by leading others and work towards common goals. You are used to a high paced work environment and got good time management skills. Qualities that we cherish are flexibility, sense of quality, friendliness, motivation to take on new challenges, grit and a sense of humor. Northvolt is an equal opportunity employer. We're a diverse group of individuals, united by a common mission, who recognise that while our actions as individuals have a role to play in driving Northvolt towards its goals, we always seek to move forward as a team. We offer you an open and welcoming atmosphere where we win as a team – and fail as a team. Northvolt is growing at the speed of light and we are a strong believer in internal career development. For us it’s important to look at your skills and potential, please refrain form including your picture and age with your application to help us with this. Apply with CV in English or your complete LinkedIn profile. Full time employment, fixed salary. Planned starting date is asap.

Job Description Quality Engineer - Quality Control LabWe are building a state-of-the-art Gigafactory that will be one of the largest battery cell production facilities in Europe. We are continuing to build our team of highly skilled Quality Engineers who will play a key role throughout the entire project lifecycle from inception through to production. Volvo Cars is one of the most well-known and respected car brands in the world. Northvolt is a leading supplier of sustainable, high-quality battery cells and systems, dedicated to delivering the world’s greenest lithium-ion battery. Together, we have formed a joint venture, NOVO Energy, to power the next generation of pure electric Volvo cars.What you will do:The factory will have a fully equipped Quality Control Lab, capable of performing a variety of analysis. As Quality Engineer working in the Quality Control Labs, you are a member of the lab team, reporting to the Manager of the lab. In your role, you will secure that products produced in the NOVO Energy plant comply to standards and specification, and by that meet customer product requirements and legislation. We are looking for Engineers for the Mechanical and Imaging section of the QC Lab. Key responsibilities will include: (but are not limited to)Define, implement and continuously improve methods, tools and equipment in the QC lab.Define and implement QMS in the lab area. Perform internal audits.Create training material and provide training to the team in quality topics. Be the owner of the equipment in the lab area, including the maintenance and calibration plans.Lead team activities such as planning, method development, problem solving and continuous improvements.Skills & Requirements:University degree in engineering and working experience within quality in a laboratory environment.Knowledge in Mechanical or Imaging Quality Control Methods and equipment. For example: CT scanning, CMMSEM, Microscopy, Tensile test Knowledge in problem solving methods & tools; 8D and 6 sigma (green belt level).Excellent English skills – written and oralAs a person you are structured, organized and meticulous with good communication skills. You are execution oriented and able to solve complex problems, as well as organize teams and competences on short notice. You have a high level of integrity, also under pressure, and are able to efficiently sort and prioritize between tasks. What’s in it for you:In this position, you will gain a deep understanding of cutting-edge battery cell manufacturing, a skill-set in high demand in an industry with immense growth ahead. To top it off, we’re gathering expertise from all over the world, and you’ll be part of an international and motivated team that have fun together while inventing for the future.