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Darmstadt, Hessen, Deutschland Bayer VollzeitJob Title: QA Manager for QC Oversight and Change ManagementAbout the Role:We are seeking a highly skilled QA Manager to join our team in Darmstadt, Germany. As a QA Manager, you will be responsible for ensuring the quality and compliance of our analytical methods and laboratory operations.Key Responsibilities:Secure QA monitoring for the validation of...
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Darmstadt, Hessen, Deutschland Bayer VollzeitJob Title: QA Manager for QC Oversight and Change ManagementAbout the Role:We are seeking a highly skilled QA Manager to join our team in Darmstadt, Germany. As a QA Manager, you will be responsible for ensuring the quality and compliance of our analytical methods and laboratory operations.Key Responsibilities:Secure QA monitoring for the validation of...
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Darmstadt, Hessen, Deutschland Bayer VollzeitJob Title: QA Manager for QC Oversight and Change ManagementAbout the Role:We are seeking a highly skilled QA Manager to join our team in Darmstadt, Germany. As a QA Manager, you will be responsible for ensuring the quality and compliance of our analytical methods and laboratory operations. You will also play a key role in implementing changes and ensuring...
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Darmstadt, Hessen, Deutschland Bayer VollzeitJob Title: QA Manager for QC Oversight and Change ManagementAbout the Role:We are seeking a highly skilled QA Manager to join our team in Darmstadt, Germany. As a QA Manager, you will be responsible for ensuring the quality and compliance of our analytical methods and laboratory operations. You will also play a key role in implementing changes and ensuring...
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Quality Assurance Specialist
vor 2 Monaten
EXCO PCC is a dynamic company that specializes in providing high-quality services to the pharmaceutical and biotechnology industries. Our team of experts is dedicated to delivering innovative solutions that meet the highest standards of quality and compliance.
Job DescriptionWe are seeking a highly skilled Quality Assurance Specialist to join our team. As a Quality Assurance Specialist, you will be responsible for ensuring the compliance of new installations or modernization projects. Your primary tasks will include defining requirements, conducting risk analyses, and overseeing the qualification and validation phases (DQ, IQ, OQ, PQ) to ensure the production of the first product batches.
Key Responsibilities- Develop and implement quality management systems to ensure compliance with regulatory requirements.
- Conduct risk assessments and develop mitigation strategies to minimize risks.
- Collaborate with cross-functional teams to ensure seamless project execution.
- Develop and maintain quality procedures and documentation.
- Identify and implement process improvements to enhance efficiency and effectiveness.
- Proven experience in quality assurance, preferably in the pharmaceutical industry.
- Strong knowledge of GMP, qualification, validation, FMEA, and pharmaceutical technology.
- Excellent communication and interpersonal skills.
- Ability to work in a fast-paced environment and prioritize multiple tasks.
- Strong analytical and problem-solving skills.
We offer a dynamic and supportive work environment, opportunities for professional growth and development, and a competitive compensation package. If you are a motivated and detail-oriented individual who is passionate about quality and compliance, we encourage you to apply for this exciting opportunity.
