MSc & PhD Chemistry Job Openings at GSK – Apply Online
GlaxoSmithKline (GSK), a global leader in pharmaceuticals and biopharmaceuticals, is hiring an Associate Specialist – MSAT (Manufacturing Science and Technology) in Bengaluru, India. This full-time role offers the opportunity to work on process validation, technology transfer, and critical risk assessments in a dynamic environment. If you are passionate about pharmaceutical innovation and want to contribute to safe and efficient drug manufacturing, this role is your perfect career move.
- Job Position: Associate Specialist – MSAT
- Location: Bengaluru, India (Luxor North Tower)
- Job ID: 427173
About the Company
GlaxoSmithKline (GSK) is one of the world’s leading global healthcare companies, dedicated to improving the quality of human life by enabling people to do more, feel better, and live longer. The company’s Manufacturing Science and Technology (MSAT) team plays a crucial role in ensuring products are manufactured to the highest safety, efficiency, and quality standards.
Education
Advanced degree in Chemistry, Chemical Engineering
Experience
- 1–5 years of experience in pharmaceutical or biopharmaceutical MSAT or related areas.
- Strong knowledge of Single Use validation, vaccines manufacturing, GMP, and GDP.
- Proficiency in validation protocols: DSR, FMEA, URS, DQ, VMP, IOQ, VSR, CRA, LRA, PES.
- Hands-on laboratory skills with the ability to manage incidents during testing.
- Project management and supplier coordination experience.
- Excellent communication, teamwork, and negotiation skills.
- Written and spoken fluency in English.
Job Description
The Associate Specialist – MSAT will manage meetings, documents, and project deliverables, as well as support process validation, risk assessments, and regulatory compliance. The role requires expertise in laboratory testing, validation protocols, and supplier management to support the manufacturing of pharmaceuticals and biopharmaceuticals.
Associate Specialist Key Responsibilities
- Prepare and manage project meetings and documentation (agenda, minutes, Team Site, TC).
- Develop laboratory mockups and create commissioning protocols for testing.
- Act as a validation expert for Single Use Systems (SUS).
- Draft Design Summary Reports (DSR) and conduct Failure Mode and Effect Analysis (FMEA).
- Develop User Requirement Specifications (URS) and manage electronic Change Control (eCC).
- Execute Design Qualification (DQ) and develop Validation Master Plans (VMP).
- Write IOQ protocols, conduct laboratory tests, and compile Validation Summary Reports (VSR).
- Perform Chemical Compatibility Risk Assessments (CRA) and Leachable Risk Assessments (LRA).
- Calculate Patient Exposure Scenarios (PES).
- Conduct BCT shipping validation testing with external labs.
- Manage purchase orders, suppliers, and GMP-compliant shipments.
- Provide weekly project progress reports to the VTT Manager.
- Ensure alignment with implementation/PPQ timelines, as well as regulatory documentation needs.
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