Project Trainee LOCQA

Position Summary
You will join our Operational Quality team in Pakistan as a Project Trainee LOCQA. You will support operational quality activities across manufacturing, packing and storage to help ensure products meet regulatory and quality expectations. You will work closely with quality, production, technical and supply colleagues to carry out checks, support investigations and help implement improvements. We value curiosity, accuracy, teamwork and a desire to learn. This role gives hands-on experience, clear learning paths and the chance to contribute to work that unites science, technology and talent to get ahead of disease together.

Responsibilities:
- Perform in-process checks and oversight during production and packing operations according to procedures.
- Support compilation, review and retention of batch documentation to enable compliant product release.
- Assist with validation activities and help implement data integrity controls.
- Help investigate deviations, support corrective and preventive actions and verify their effectiveness.
- Manage sample handling, line clearance and archive activities to meet record retention requirements.
- Contribute ideas and support continuous improvement for safer, leaner and more reliable processes.

Basic Qualification
- Bachelor’s degree in Pharmacy (Pharm-D), B. Pharm, Chemistry, Life Sciences or a related field.
- 0 to 1 year relevant experience; fresh graduates with internships are welcome.
- Basic understanding of Good Manufacturing Practices and good documentation practices.
- Proficient in Microsoft Office: Word, Excel, PowerPoint and Outlook.
- Strong attention to detail and ability to follow procedures consistently.
- Good communication skills and ability to work collaboratively in a team.
- Internship experience in pharmaceutical or consumer healthcare quality or manufacturing.
- Familiarity with batch record review, sample retention and line clearance processes.
- Basic knowledge of validation protocols and data integrity principles.
- Analytical mindset with problem solving and root cause analysis skills.
- Ability to manage multiple tasks and work under pressure.
- Willingness to learn, coach others and contribute to continuous improvement.

Working arrangement
This is an on-site role based in Pakistan. You will work at the manufacturing site and engage directly with cross-functional teams.

Skills

Data Integrity, Detail-Oriented, Digital Fluency, GxP Regulations, Lean Management, Pharmaceutical Regulatory Compliance, Problem Solving, Quality Assurance (QA), Risk Awareness, Technical Writing

 

 

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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