GSK

Assistant Manager Stability Operations

Pakistan - Sindh - Karachi Full time

You will lead stability operations to ensure studies run on time, meet quality standards and support product supply. You will work closely with laboratory, quality, production and engineering teams. We value practical problem-solvers who act with integrity, communicate clearly and focus on continuous improvement. This role offers hands-on learning, visible impact and the chance to grow while contributing to GSK’s mission of uniting science, technology and talent to get ahead of disease together.

Responsibilities
- Plan, schedule and perform stability testing on time according to approved stability plans.
- Prepare, maintain and update the Master Stability Schedule and related records.
- Execute test methods and document results following procedures and data integrity expectations.
- Investigate out-of-specification or atypical results and support corrective and preventive actions.
- Manage chamber monitoring, respond to excursions, and support equipment calibration and maintenance.
- Support protocol preparation, stability data evaluation and cross-functional readiness for new product launches.

- Ensure and lead Data Integrity in department and perform monthly Management Monitoring and ensure timely closure of VQD CAPAs and related action items.

Education, Experience and Skills

- Pharm – D, Bachelor’s or Master’s degree in Chemistry / Applied Chemistry, Microbiology or related science discipline.

- 3 to 5 years’ experience in pharmaceutical stability, quality control or related laboratory role.

- Practical experience with routine analytical testing and documentation.

- Working knowledge of good manufacturing practices and laboratory quality systems.

- Proficiency in MS Office applications and ability to use electronic records or laboratory systems.

- Strong communication, organization and record-keeping skills with attention to data integrity.

- Experience with equipment qualification and validation activities (IQ/OQ/PQ).

- Hands-on experience with stability chamber management and environmental monitoring.

- Familiarity with SAP or other ERP/LIMS for sample and inventory management.

- Previous involvement in investigations, CAPA execution or internal audits.

- Experience preparing and reviewing stability protocols and trend analysis.

- Commitment to continuous improvement and collaborative problem-solving.

How to apply

We want to hear from you. If this role matches your skills and ambitions, please apply today and tell us how you will contribute to the team and our mission.

Why GSK?
Uniting science, technology and talent to get ahead of disease together.

GSK is a global biopharma company with a purpose to unite science, technology and talent to get ahead of disease together. We aim to positively impact the health of 2.5 billion people by the end of the decade, as a successful, growing company where people can thrive. We get ahead of disease by preventing and treating it with innovation in specialty medicines and vaccines. We focus on four therapeutic areas: respiratory, immunology and inflammation; oncology; HIV; and infectious diseases – to impact health at scale.

People and patients around the world count on the medicines and vaccines we make, so we’re committed to creating an environment where our people can thrive and focus on what matters most. Our culture of being ambitious for patients, accountable for impact and doing the right thing is the foundation for how, together, we deliver for patients, shareholders and our people.

Contact information:
You may apply for this position online by selecting the Apply now button.

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