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5 days ago
In this role, you will be part of a talented team dedicated to developing and manufacturing innovative therapies. You will have the opportunity to work on complex projects, develop new skills, and contribute to our mission.
The QC Manager will lead and inspire our Quality Control team to achieve analytical excellence and compliance. This involves overseeing analytical method development, validation, and impurity profiling to ensure regulatory compliance.
Key areas of responsibility include:
- Developing and implementing process optimization initiatives to improve efficiency, reliability, and scalability in testing.
- Coordinating cross-functional efforts with R&D and manufacturing teams to support product development milestones.
- Fostering a culture of quality and continuous improvement within the Quality Control team.
- Ensuring compliance with GMP standards and leading efforts during audits and regulatory inspections.
Requirements for success include:
- Degree in a relevant scientific field (e.g., chemistry, pharmacy, or related discipline).
- Extensive experience in a GMP-regulated pharmaceutical environment, with a strong focus on analytical development.
- Proven leadership experience, with the ability to motivate and manage diverse teams.
- Expertise in analytical techniques and regulatory standards such as ICH Q3C, Q3D, and USP.
- Exceptional organizational and communication skills, with a proactive and problem-solving mindset.
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