My client is looking for a QA Manager External Supply to be responsible for the release of products (bulk and finished) supplied by the Contract Manufacturing Organizations (CMO) as well as for the establishment and maintenance of Quality Assurance release processes. This is new created position - permanent - based in Basel, Switzerland.
Main responsibilities
- To write, edit, assess and approve GMP and regulatory relevant documents related to product quality (e.g. SOP, deviation/investigation reports, complaints) as well as the support and involvement in internal and external audits are your main tasks.
- The efficient handling of quality issues related to release activities, the communication and cooperation with internal and external partners and the participation in Local and Global Expert Meetings rounds off your scope of duties.
Main Qualifications
- You have a University degree in pharmacy and professional experience gained within the pharmaceutical, biotechnology or medical device industry.
- First experience in Quality Management is a plus.
- Conversational German mandatory (you need to discuss with people from the production site). Good English and good knowledge of French are considered beneficial.
- Ambitious, achievement-oriented and reliable collaborative team player combined with a well structured working style as well as excellent communication and interpersonal skills.
This job was posted 30+ days ago, and has expired.