...QA roles within the medical device industry.Proven expertise in ISO 13485:2016, EU MDR 2017/745, and applicable standards (e.g., ISO 14971, IEC 62304).Experience with Class IIa/IIb or Class III device... (talent.com)
...QA check rounds and support optimization projects and tasks.Maintain strong stakeholder relationships across Business and Quality teams.What we are looking forMaster’s degree in a scientific field.Exp... (talent.com)
...scientific fieldSignificant experience in pharmaceutical or biotech GMP environmentsStrong understanding of regulated manufacturing and/or biopharmaceutical developmentPrevious exposure to customer-fa... (talent.com)
...scientific field Significant experience in pharmaceutical or biotech GMP environments Strong understanding of regulated manufacturing and/or biopharmaceutical development Previous exposure to customer... (jooble)
...scientific data. The role is predominantly lab-based and requires strong technical autonomy. Non-Negotiable Skills, Qualifications, and Experience • Master’s degree in Analytical Chemistry, Organic Ch... (jooble)
...scientific data. The role is predominantly lab-based and requires strong technical autonomy. Non-Negotiable Skills, Qualifications, and Experience • Master’s degree in Analytical Chemistry, Organic Ch... (jooble)
.../MSAT for Pharma Drug Substances and Drug Products. Provide expert QA advice, support and management for technical operational QA and general QA matters associated with Internal & External Pharma A/MS... (jooble)
...QA roles within the medical device industry . Proven expertise in ISO 13485:2016 , EU MDR 2017/745 , and applicable standards (e.g., ISO 14971, IEC 62304). Experience with Class IIa/IIb or Class III d... (jooble)
...QA roles within the medical device industry . Proven expertise in ISO 13485:2016 , EU MDR 2017/745 , and applicable standards (e.g., ISO 14971, IEC 62304). Experience with Class IIa/IIb or Class III d... (jooble)
...QA roles within the medical device industry . Proven expertise in ISO 13485:2016 , EU MDR 2017/745 , and applicable standards (e.g., ISO 14971, IEC 62304). Experience with Class IIa/IIb or Class III d... (jooble)
...QA roles within the medical device industry . Proven expertise in ISO 13485:2016 , EU MDR 2017/745 , and applicable standards (e.g., ISO 14971, IEC 62304). Experience with Class IIa/IIb or Class III d... (jooble)
...QA roles within the medical device industry . Proven expertise in ISO 13485:2016 , EU MDR 2017/745 , and applicable standards (e.g., ISO 14971, IEC 62304). Experience with Class IIa/IIb or Class III d... (jooble)
.../FT) Assurer la fonction de DPO (registre, politiques, DPIA, accompagnement des équipes) Suivre les obligations DDA via la FSMA / plateforme Cabrio Rédiger, analyser et négocier les contrats avec part... (adzuna)
...scientific data. The role is predominantly lab-based and requires strong technical autonomy.Non-Negotiable Skills, Qualifications, and Experience• Master’s degree in Analytical Chemistry, Organic Chem... (talent.com)
.../MSAT for Pharma Drug Substances and Drug Products. Provide expert QA advice, support and management for technical operational QA and general QA matters associated with Internal & External Pharma A/MS... (talent.com)