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ContactWorking timeFull-time LocationDatteln Start dateas soon as possible / by agreement Contractpermanent employment
EN
Your tasks with us.
- Process and assess deviations, CAPA actions and quality-related changes.
- Review and approve GMP documents, standard operating procedures and manufacturing records.
- Prepare and support internal and external audits and inspections.
- Advise specialist departments on quality-related questions.
- Further develop the pharmaceutical quality system and its key performance indicators.
What you bring with you.
- A degree in natural sciences or pharmacy, or a comparable qualification.
- Professional experience in quality assurance, quality control or manufacturing in a GMP environment.
- Confidence in regulatory requirements and quality documentation.
- An analytical, solution-oriented approach and clear communication.
- A strong sense of responsibility and enjoyment of cross-functional collaboration.
What we offer you.
- Family-owned company: A secure, permanent position with long-term prospects, respectful collaboration and short decision paths.
- Health & benefits: Attractive compensation, 30 days of annual leave, employer-supported pension benefits and JobRad bicycle leasing.
- Development & training: Structured onboarding and financial support for external specialist training courses and seminars.
Attractive package
What we offer.
Confidential handling
Application data and documents are processed solely for the application procedure.
Confirmation of receipt
After submission, receipt of the application is confirmed automatically by email.
Personal review
Applications are reviewed internally and are not evaluated automatically.
Apply in just a few minutes.
Open our online application portal and submit your documents in a few clear steps.