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À propos
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Our client is seeking a dynamic Validation Engineer to join their cutting-edge Manufacturing Science and Technology (MSAT) team.
The Validation Engineer will play a crucial part in ensuring the highest standards of quality and compliance in the production of life-changing medications.
If you have 2 + years of experience in Validation in the pharmaceutical or biotechnology industry and are ready for your next challenge, this could be the perfect opportunity for you! RESPONSIBILITIES: Lead cleaning validation studies, leveraging your expertise to maintain impeccable standards Spearhead process improvement projects and investigations, driving efficiency and innovation Develop and review critical MSAT documentation, ensuring compliance with US and EU regulations Collaborate with cross-functional teams to optimize manufacturing processes Represent the site MSAT team on platform technical teams, showcasing your leadership skills EDUCATION/EXPERIENCE: Degree in Engineering, Molecular Biology, Biochemistry, Pharmacy, or related scientific field Minimum 2 years' experience xcfaprz in Large Molecule manufacturing industry Extensive knowledge of FDA/EMEA regulatory requirements Strong background in cleaning validation studies and strategies (2+ years preferred) Excellent communication, leadership, and problem-solving skills Ability to thrive in a fast-paced, dynamic environment Apply via this advert or contact Kathy Gillen LSC on if you have any more questions about this role!
Compétences linguistiques
- English
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