GSK

biopharma

Intern(Quality)

Pakistan FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Entry candidates.

The Brief

“Intern (Quality) at GSK. Skills: Quality Control, Analytical techniques, GMP. Observe routine testing. Verify compliance”

What You'll Achieve.

Ensure quality standards; Ensure safety standards; Ensure regulatory standards; Maintain product integrity; Achieve departmental objectives

Industry & Context.

biopharma
Problems you'll solve

Troubleshooting

What They're Looking For.

Must Have

Basic understanding of pharmaceutical sciences, Basic understanding of chemistry, Basic understanding of microbiology, Interest in quality control, Interest in laboratory testing, Interest in GMP implementation, Willingness to learn analytical techniques, Awareness of safe storage, Awareness of organized storage, Attention to detail, Documentation discipline, Focus on product quality, Focus on product safety, Ability to work collaboratively, Support departmental projects

Nice to Have

HPLC, Spectrophotometry, Microbiological methods

What You'll Do.

Observe routine testing

Support impurity identification

Support contaminant identification

Develop understanding of regulatory requirements

Support GMP implementation

Contribute to continuous improvement

Observe microbiological testing

Build understanding of quality control principles

Build understanding of documentation practices

Support stability studies

Contribute to departmental objectives

Contribute to quality projects

How You'll Work.

Team & Collaboration

Collaborate with cross-functional teams; Work with Production; Work with QA; Work with Microbiology; Work with Engineering

Full Job Description

**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

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