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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.
Apply in just a few minutes.
Open our online application portal and submit your documents in a few clear steps.