Überblick über die Statistik des Gehaltsniveaus für "Quality Control 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 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Für unsere Abteilung Quality Control in Marburg suchen wir aktuell einenSenior Manager Quality Control Marburg - Microbiology (m/w/x) - R-228886(Vollzeit / unbefristet / AT Level 7) Rolle: Leitung des Labors Mikrobiologie in der Qualitätskontrolle zur Durchführung von Analysen entsprechend den GMP-RegularienFührung des LaborpersonalsFachliche Verantwortung für die Analysenmethoden„Leiter der Qualitätskontrolle“ nach AMWHVIhre Aufgaben: Sicherstellen der GMP-konformen, termingerechten Durchführung und Dokumentation von qualitätsrelevanten Prüfungen an In-Prozess-Kontrollen, Wirkstoffen und EndproduktPlanung, Steuerung und Reporting der Performance des LaborsLdQ entsprechend § 12 AMWHVFachlicher Experte für den geführten Laborbereich (wissenschaftliche / technische Leitung des Labors)Vertretung des Labors gegenüber Behörden und bei AuditsPlanung und Ausführung von Untersuchungen / Studien, die einen fachlichen Schwerpunkt im Verantwortungsbereich haben (z.B. bei Auffälligkeiten in den Produktionsbetrieben oder bei der Bearbeitung von Abweichungen und PTRs)Führung der laborspezifischen Dokumentationssysteme (SOPs, Prüfanweisungen, Durchführungsprotokolle, etc.)Optimieren der Arbeitsabläufe im Labor unter Berücksichtigung der Entwicklung des Produktportfolios, kosten- und qualitätsrelevanter Aspekte, gesetzlicher und regulatorischer Anforderungen, Optimierungspotential in der eigenen OrganisationPersonalbedarfsplanung sowie Personaleinsatzplanung und Personalbestandskontrolle im VerantwortungsbereichFühren der unterstellten Mitarbeiter entsprechend den Führungsgrundsätzen des UnternehmensPlanen und Kontrolle des Budgets für den Verantwortungsbereich in Abstimmung mit dem Vorgesetzten und dem Controlling und ggf. Ergreifen von geeigneten Korrekturmaßnahmen bei Soll-/Ist-Abweichungen.Sicherstellen der Einhaltung interner und gesetzlicher Regelungen zu Arbeitssicherheit und ArbeitsschutzFührung von fachspezifischen Projekten und Mitarbeit bei internen, standortweiten oder globalen ProjektenQualifikationenBachelor-Abschluss in einer relevanten wissenschaftlichen Disziplin (Biologie, Mikrobiologie, Chemie usw.) mit fundierten mikrobiologischen Kenntnissen; höherer Abschluss bevorzugtMindestens 7 Jahre Erfahrung in der mikrobiologischen und biologischen, chemischen oder biochemischen Analytik im pharmazeutischen/medizinischen GMP-UmfeldNachgewiesene Management-/FührungserfahrungKenntnisse über Testmethoden und MethodenvalidierungSehr gute Kommunikations- und PräsentationsfähigkeitenSehr gute Englischkenntnisse in Wort und SchriftOur 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!

Du leitest die Mitarbeitenden in der Qualitätskontrolle und stellst sicher, dass die Prozesse, die Unternehmensrichtlinien und die entsprechenden Verfahren eingehalten werdenDu stellst sicher, dass deine Mitarbeitenden für ihre jeweilige Funktion angemessen geschult wurden und mit dem Qualitätsmanagementsystem sowie den funktionsrelevanten Verfahren für die Qualitätsprüfung in der Luftfahrt vertraut sindDu stellst unsere Lieferfähigkeit hinsichtlich Qualitätssicherheit und -anforderungen sicherDu unterstützt die Fachbereichsleitung bei der Definition, Einführung und Umsetzung von Maßnahmen im Rahmen kontinuierlicher VerbesserungsprozesseDu bist gerne nah am Produkt und arbeitest gerne auch selbst in der Qualitätskontrolle mitUnd weitere spannende Aufgaben und Herausforderungen erwarten dich bei unsEine Stellenanzeige von Adient Aerospace Seating GmbH

Job Description We are looking for Quality Control Technicians to join us in our mission to build the world’s greenest battery. The role is a part of our Revolt Ett team based in Skellefteå / Västerbotten. About the jobWe are looking for driven people with a laboratory experience who preferably have background in the industrial sampling and testing. The persons we are looking for are systematic and eager to learn.In your role, you will work in chemical laboratory performing various analyses and tests of incoming materials as well as production samples.Our production will run 24/7 including weekdays, weekends and all the holidays. The shifts will rotate between morning, evening and nights and we need you to be able to rotate between all the shifts.You will get the chance to have a real impact on our success story in Sweden and see the results of your work! About the teamThe QC team should be the experts, having experience in receiving samples, measuring methods, samples preparation, and result reporting. Your team will play an important role in supporting the production team in measuring and improving our product quality. QC team will be developing, validating, defining, and implementing the inspection methods for all tested materials. Furthermore, the team will be responsible for Measurement System Analysis and work with the R&D group to evaluate and compare product quality (it includes participation in Root Cause Analysis). Key responsibilities include but are not limited to:Perform samplings and prepare material for testing.Perform routine quality control tests and measurements ensuring that incoming material/product meet quality specifications. Operate various analytical techniques including ICP-OES, ICP-MS, XRF, pH measurements, titrations, oven, etc.Interpret data and report the results. Apply with CV and cover letter or your complete LinkedIn profile. Full time employment, fixed salary.Planned starting date is as soon as possible.

Job Description We are looking for an experienced Senior Quality Control Engineer-CT to join us in our mission to contribute to a greener future. The role is a part of our excellent Quality team based in Skellefteå. By joining us, you will be a key player in establishing and one of the first large scale European battery factories. About the jobYou will be responsible for the development, validation, and implementation of the methods used for computed tomography and other non-destructive test methods. Adherence to the principles of Quality Assurance in QC. Proven track record in statistical analysis and measurement system analysis (MSA).Key responsibilities include but are not limited to:•Develop, validate and document methods and procedure for scanning and analyzing intermediate and final products from battery cell production• Performing special scan requests for battery cells and their components on Computed Tomography and X-Ray systems (e.g. Waygate, Nikon, Exacom)• Performing problem solving and improvement activities for scanning activities and its records aswell as updating work instructions• Optimize methods to increase efficiency and turn-around time of the laboratory.• Working with instrument suppliers and machine builders for designing custom fixtures,instruments & automation• Inputs for laboratory planning of expansions and related sourcing of additional equipment andinstruments• Train team members on instrument usage, analysis and troubleshooting activities• Provide guidance and specialist knowledge for product families or processes• any other duties and responsibilities required to deliver on company objectives Accountability/Authorization • Budget responsibility: N• Direct reports: N• Authorized to decide on investments according to role and policy. Apply with CV in English or your complete LinkedIn profile.Full time employment, fixed salary. Planned starting date is asap.

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.

Deine BenefitsSpannende, selbstorganisierte und eigenverantwortliche AufgabenLangfristiges Arbeitsverhältnis, angenehmes Betriebsklima in einem jungen, engagierten TeamGleitzeitvereinbarung, flexibles Arbeitszeitmodell, Work-Life-BalanceSpezialisierungsmöglichkeiten sowie fachspezifische Weiterbildungen und TrainingsAusgesprochen kollegiales Team mit freundschaftlicher UmgangsweiseVielfältige Entwicklungsmöglichkeiten innerhalb der TECCON GroupDas Bruttojahresgehalt beträgt mindestens EUR 40.000€, selbstverständlich bieten wir jedoch eine marktkonforme Überbezahlung in Abhängigkeit von der Qualifikation und Berufserfahrung.Dein ProfilAbgeschlossene Fachausbildung (z.B. Chemielaborant, HTL Chemietechniker oder äquivalente Ausbildung)Sehr gute Deutschkenntnisse sowie Basiskenntnisse in EnglischErste praktische Berufserfahrung im Rahmen der Ausbildung im Pharmabereich bzw. in der WirkstoffherstellungErste HPLC und Chromeleon Erfahrung von VorteilTeamfähigkeit, analytisches Denken, strukturierte ArbeitsweiseDeine AufgabenGMP-gerechte Durchführung, Auswertung und Dokumentation von Analysen (Inprocess, Freigabe, Stabilität, Sonderanalysen) und den damit verbundenen TätigkeitenBeachten von analytischen Qualitätskontrollen (System Suitability Tests, Kontrollproben etc) zur Gewährung der Richtigkeit und PräzisionEingabe der Analysenresultate in das SAP-System, Ablage und ArchivierungPermanentes Überwachen von zugewiesenen Analysenmethoden mit Trendkontrolle von DatenWarten und Kalibrieren von Analysengeräten mit begleitender Dokumentation und TerminkontrolleBetreuung von Analysengeräten (zB. pH-Meter) aber auch on-line Analysensystemen (z.Bsp. HPLC) in ProduktionslaborenRechtzeitige Information des Prüfgruppenleiters bzw. des Laborleiters bei auffälligen Analysenwerten oder Überschreitung von GrenzwertenMitarbeit an der Qualifizierung von Analysengeräten mit begleitender Dokumentation und TerminkontrolleQC Analyst (m/w/d)Als TECCON Austria haben wir uns auf die Themenbereiche Automotive Passive Safety und Beratungsdienstleistungen spezialisiert. Wir arbeiten eng mit namhaften OEMs zusammen, um innovative Lösungen zu entwickeln und die Sicherheit von Fahrzeugen zu verbessern. Darüber hinaus bieten wir auch Beratungsdienstleistungen in den Bereichen Rail, Automotive, Pharma, IT und Anlagenbau an. Unser Ziel ist es, unseren Kunden maßgeschneiderte Lösungen anzubieten und sie bei der Optimierung ihrer Prozesse zu unterstützen.1998 als Concept Tech GmbH in Gratkorn gegründet, sind wir heute ein wichtiger Teil der Hamburger TECCON Gruppe und entwickeln zusammen mit mehr als 450 Ingenieuren, Technikern und IT-lern die Lösungen für die Zukunft. Dafür verfügt die Gruppe über acht Kompetenzeinheiten, die im regen Austausch stehen und auch interdisziplinäre Projektteams bilden, um optimale Ergebnisse zu erzielen.Eine Stellenanzeige von Teccon Austria GmbH#catchbasic