GMP Specialist
vor 1 Tag
About the Role
We are seeking a highly skilled GMP Specialist to join our team at GULP – experts united. As a key member of our team, you will be responsible for ensuring the highest standards of quality and compliance in our pharmaceutical operations.
Key Responsibilities
- Assume factual processes with own disposition authority in the field of control, planning, and processing of batch papers, batch record review.
- Comply with GMP-compliant working methods in the laboratory complex.
- Carry out tasks in various areas of drug testing, including chemical and physical quality tests as part of release tests on intermediate products and finished medicinal products.
- Check finished medicinal products for appearance and completeness, and label them in accordance with the requirements of the approval documents.
- Properly enter and remove retained samples, documenting and evaluating test and inspection results.
- Compile the batch documentation into a complete batch record.
Requirements
- Completed technical or scientific vocational training, including proven further training qualification, e.g., in the fields of pharmaceutical and chemical engineering or pharmaceutical chemistry.
- Very good knowledge of general GMP requirements.
- Sound professional experience in the field of Batch Record Review is an advantage.
- Experience in the field of drug analysis, in the application of applicable GMP regulations or drug technologies.
- Very good German and good written and spoken English skills.
- Ability to work in a team as well as a structured and independent way of working.
- Initiative, assertiveness, and a sense of responsibility.
About Us
GULP – experts united is a leading provider of professional solutions in the pharmaceutical and chemical industries. We value equal opportunities and welcome applications from people with disabilities.
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