experience: QA experience in a Pharmaceutical Company for 3-5 years with involvement in QA activities. Experience
Over de functie We are looking for a dynamic, hands-on individual who shares our passion for conservation and will accept the challenge of supervising the QA team. You have to be VERY HANDS ON and take responsibility for the following duties: • oversee quality operations and supervise the QA team
Key Outputs: Assist with external audits were necessary; compile reports and follow-up on CAPAParticipate in risk assessments on QMS and departmental processes to assess risk and identify mitigating actions and controlsConduct root cause investigations into incidents and deviations identifying root
Sciences 5-10 years experience in Pharmaceutical production environment in QA, QC, Validation and sterile manufacture
within the Pharmaceutical Industry is essential.Previous experience having worked within a QA/QC management
relevant business area e.g. Pharmaceutical Manufacturing (Production / QA / Technical Support) or 1 –
activities within the Pharmaceutical Quality occur Overall management of specified QA processes: Deviations