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Job description
The Associate Manager, QA Biologics will play a key role in ensuring the quality of biologics products, providing guidance and support during project phases and routine GMP operations. The role involves developing and maintaining quality documentation, evaluating suppliers, and performing risk assessments.
The successful candidate will be responsible for ensuring product quality issues are investigated and corrected, reviewing deviation reports, and supporting audits and inspections. They will also participate in tech transfer, collaboration with other functions, and support compliance and regulatory activities.
The ideal candidate will have a degree in pharmaceutical sciences or a related field, with at least 7 years of experience in quality assurance, GMP compliance, or operations. They will be able to logically solve problems, interact with various personalities, and communicate effectively in English.
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Healthcare
Roche, founded in 1896, is a global leader in pharmaceuticals and diagnostics that integrates research, development, and manufacturing to deliver personalized healthcare solutions. The company’s core portfolio spans oncology, immunology, infectious diseases, ophthalmology, and CNS disorders, while its diagnostics arm dominates in vitro and tissue-based cancer testing and diabetes management. Roche’s commitment to precision medicine is reflected in its 30 essential medicines on the WHO Model List and its reputation as a sustainability pioneer in the life sciences sector. With a culture that values scientific innovation, patient access, and collaborative impact, Roche offers career opportunities that drive meaningful change in global health.