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Scientist IMP In-Process Controls
- Contract
- Manufacturing
- Switzerland
Help bring science to life and join a leading pharmaceutical company to play a key role in delivering impactful research that drives healthcare innovation!
ذكذكتسئµ is seeking a Scientist IMP In-Process Controls to join the Manufacturing Analytics Team in Basel. In this role, you will play a key part in ensuring the quality and integrity of analytical processes during the manufacturing of chemically synthesized Active Pharmaceutical Ingredients (APIs). This position requires a proactive individual who can seamlessly implement new methods, maintain rigorous documentation standards, and contribute to process optimization within a cGMP-regulated environment.
Please note that to be considered for this role you must have the right to work in this location or hold an EU passport.
Responsibilities:
- Guide laboratory colleagues in planning, executing, and concluding analytical tests for in-process and intermediate analytics.
- Ensure compliance with cGMP, safety standards, and regulatory requirements in all analytical activities.
- Review analytical methods and specifications from the analytical development department.
- Implement and establish new analytical methods into production-accompanying control processes.
- Generate and review analytical documentation with a focus on quality, data integrity, and meeting deadlines.
- Manage and document deviations and non-conformances proactively and efficiently.
- Participate in quality assessments and investigations to uphold product integrity.
- Assist in developing and implementing lean, efficient working processes to optimize operations.
Key Skills and Requirements:
- A Master's degree or equivalent in Natural Sciences, or a Chemical Laboratory Technician apprenticeship with relevant professional experience.
- Hands-on experience with analytical techniques, particularly chromatography, in chemical manufacturing processes.
- Strong commitment to quality, data integrity, and accurate documentation.
- Solid understanding of GMP principles and regulatory requirements in the pharmaceutical industry.
- Proficiency in German (C1 level) and English to navigate a dynamic, matrix organization.
- Excellent organizational skills with the ability to manage and prioritize multiple tasks effectively.
- A proactive team player with a strong sense of responsibility and adaptability.
If you are having difficulty in applying or if you have any questions, please contact Ashley Bennett at a.bennett@proclinical.com.
If you are interested in applying to this exciting opportunity, then please click 'Apply' or to speak to one of our specialists please request a call back at the top of this page.
ذكذكتسئµ is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. ذكذكتسئµ is acting as an Employment Agency in relation to this vacancy.
By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - /privacy-policy.
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