Quality Control Lead (Sterile Product Manufacturing)

Biogen
Athlone, Leinster, Ireland
Full Time
On Site
Manager
0+
Bachelor Degree
Healthcare Healthcare Life Sciences

Posted 2 days ago

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Excellent 4.7

Job summary

Lead Quality Control operations in sterile pharmaceutical manufacturing, ensuring compliance with regulatory standards, overseeing testing processes, and managing laboratory and personnel to maintain GMP standards.

Responsibilities

The Quality Control Lead will oversee site-wide QC operations, including laboratory management, environmental monitoring, and product release in compliance with GMP and regulatory standards. They will also lead the establishment of QC processes, manage department budgets, and foster cross-functional partnerships to support new technology introductions.

Qualifications

Analytical methods GMP compliance Laboratory setup and maintenance Method transfer and validation Microbiological Analysis Personnel management Project management Quality Control Regulatory standards (EU GMP, FDA)

Candidates must hold a Bachelor's degree in Science or a related discipline and possess significant experience in GMP-compliant Quality Control or analytical functions within the pharmaceutical or biotech industry. Strong leadership, personnel management, and technical expertise in microbiological analysis and method validation are essential.

English

Company

Biogen

Biogen

linkedin
Biotechnology Research
Location
Athlone, Leinster, Ireland
Website
biogen.com

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Excellent 4.7
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