Descrizione dell'offerta
Quality Assurance Specialist (m/f/d)
Bayer Healthcare Manufacturing is looking for a newly graduated and motivated Quality Assurance Specialist to join our team at the Garbagnate Milanese production site, within the Quality Assurance department. Responsibilities
Batch production documentation review, utilizing electronic batch records. Preparation of data and reports for Product Quality Reviews (PQR), Ongoing Process Verification (OPV), and distribution based on the annual calendar. Preparation of documents relevant to batch disposition and market supply, e.g., CoA and CoC. Participation in the QA team activities: GEMBA walks, QA on the shop floor, and oversight of calibration and maintenance activities. Management/update of procedures. Management of batch documentation and archiving. Support in the management of site GMP training records and GMP documentation using electronic management systems. Qualifications
Degree in Chemistry, Pharmaceutical Technologies, or Pharmacy. Knowledge of GMP. Fluent in English and Italian. Excellent knowledge of the Microsoft Office Package. Teamwork orientation, initiative spirit, precision, and sense of responsibility. Minimum of 1 year in QA; experience in a pharmaceutical company in production and/or QA is a plus. Benefits & Compensation
We are committed to paying compensation based on gender-neutral criteria and in all cases on objective, fair and performance-based criteria. The initial annual gross compensation for this role is not below 34,984.04 EUR. Any upward adjustments may be made in the presence of objective circumstances, such as experience, specific qualifications, and/or specific areas of responsibility. Location: Garbagnate, Italy (Garbagnate Milanese) Contract type: Fixed-term contract 12 months, full-time.
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Bayer Healthcare Manufacturing is looking for a newly graduated and motivated Quality Assurance Specialist to join our team at the Garbagnate Milanese production site, within the Quality Assurance department. Responsibilities
Batch production documentation review, utilizing electronic batch records. Preparation of data and reports for Product Quality Reviews (PQR), Ongoing Process Verification (OPV), and distribution based on the annual calendar. Preparation of documents relevant to batch disposition and market supply, e.g., CoA and CoC. Participation in the QA team activities: GEMBA walks, QA on the shop floor, and oversight of calibration and maintenance activities. Management/update of procedures. Management of batch documentation and archiving. Support in the management of site GMP training records and GMP documentation using electronic management systems. Qualifications
Degree in Chemistry, Pharmaceutical Technologies, or Pharmacy. Knowledge of GMP. Fluent in English and Italian. Excellent knowledge of the Microsoft Office Package. Teamwork orientation, initiative spirit, precision, and sense of responsibility. Minimum of 1 year in QA; experience in a pharmaceutical company in production and/or QA is a plus. Benefits & Compensation
We are committed to paying compensation based on gender-neutral criteria and in all cases on objective, fair and performance-based criteria. The initial annual gross compensation for this role is not below 34,984.04 EUR. Any upward adjustments may be made in the presence of objective circumstances, such as experience, specific qualifications, and/or specific areas of responsibility. Location: Garbagnate, Italy (Garbagnate Milanese) Contract type: Fixed-term contract 12 months, full-time.
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