GSK
biopharma
Intern(Quality)
Neural analysis suggests this role is
optimal for Entry candidates.
“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.
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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