Biopharma Quality Investigations Expert
vor 1 Woche
At Randstad Inhouse Services, we are looking for a highly skilled Biopharma Quality Investigations Expert to join our team in Bern, Switzerland.
About the RoleThis is a 12-month fixed-term contract position that will involve leading non-conformance investigations, performing root cause analysis, and implementing corrective actions to prevent recurrence. The ideal candidate will have a strong background in biopharma production environments regulated by cGMP standards and excellent analytical thinking and problem-solving skills.
Key Responsibilities- Lead non-conformance investigations from initiation to closure, including performance of impact assessments and implementation of corrections and preventive actions.
- Gather data from various sources, perform root cause analysis, and identify assignable causes.
- Develop and implement corrective actions to prevent recurrence, working closely with operations, quality control, and assurance departments.
- Write technical reports on investigation findings, communicating complex information to an educated but uninformed audience.
To be successful in this role, you will need:
- A bachelor's or advanced degree in chemistry, biochemistry, pharmacy, or a relevant scientific discipline.
- At least 3 years of experience in biopharma production environments regulated by cGMP standards, preferably in manufacturing operations and/or quality control.
- Excellent analytical thinking and problem-solving skills, combined with good teamwork capabilities.
- Proficiency in English is required, German language skills are desirable but not mandatory.
We offer a competitive salary package, which includes an estimated salary of CHF 85,000 - CHF 105,000 per year, depending on experience and qualifications. Additionally, you will benefit from working with a global leading pharmaceutical company in a dynamic, progressive, and collaborative environment.
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