Intern (Quality)

Role Summary

The role supports the Quality Control (QC) / Quality function by observing and assisting in routine testing of raw materials, intermediates, and finished products to ensure they meet quality, safety, and regulatory standards. It involves learning and applying GMP and quality control principles, supporting impurity/contaminant identification, microbiological and stability testing, use of analytical techniques (e.g., HPLC, spectrophotometry), and contributing to departmental objectives through cross-functional collaboration.

Key Responsibilties

• Observe routine testing of raw materials, intermediates, and finished products to verify compliance with defined quality specifications.

• Learn and support activities related to identifying impurities and contaminants to maintain product integrity.

• Develop understanding of applicable regulatory requirements, guidelines, and GMP and support their implementation in daily work.

• Contribute to the continuous improvement of product quality and safety.

• Observe microbiological testing to ensure product sterility where applicable.

• Build understanding of quality control principles, methodologies, and documentation practices.

• Learn to analyze samples using techniques such as HPLC, spectrophotometry, and other relevant analytical methods.

• Support and focus on stability studies to assess and monitor product shelf life.

• Contribute to the implementation of departmental objectives and quality projects.

• Collaborate with cross-functional teams (e.g., Production, QA, Microbiology, Engineering) for troubleshooting and problem-solving.

Education & Skills

• Pharmacist / Chemist / Microbiologist / Science undergraduate

• Basic understanding of pharmaceutical sciences, chemistry, microbiology, or related scientific disciplines.

• Interest in quality control, laboratory testing, and GMP implementation.

• Willingness to learn analytical techniques (HPLC, spectrophotometry, microbiological methods).

• Awareness of safe and organized storage of pharmaceutical products and operations.

• Attention to detail, strong documentation discipline, and focus on product quality and safety.

• Ability to work collaboratively with cross-functional teams and support departmental projects.

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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