GSK
biopharma
Intern(Engineering)
Neural analysis suggests this role is
optimal for Entry candidates.
“Intern (Engineering) at GSK. Skills: equipment maintenance, calibration, reliability, process optimization. Support pharmaceutical manufacturing operations. Assist in maintenance, calibration, and reliability”
Industry & Context.
Analytical mindset focused on efficiency, OEE improvement, and process optimization
What They're Looking For.
Must Have
BE (Bachelor of Engineering), Basic understanding of pharmaceutical/ manufacturing operations and engineering systems, Knowledge or willingness to learn GMP, GES standards, and regulatory compliance, Interest in equipment maintenance, calibration, validation, and reliability, Analytical mindset focused on efficiency, OEE improvement, and process optimization, attention to detail, documentation discipline, safety awareness, Ability to work collaboratively with Engineering and Operations teams, follow planned activities
What You'll Do.
Support pharmaceutical manufacturing operations
Assist in maintenance
Contribute to process optimization initiatives
Support improvement of OEE and equipment efficiencies
Learn and support equipment validation activities
Understand and help improve equipment reliability
Observe and support planned engineering activities
Learn and follow Engineering quality system
Adhere to Good Documentation Practices
Support implementation of departmental objectives
How You'll Work.
Team & Collaboration
Ability to work collaboratively with Engineering and Operations teams
Full Job Description
**Role Summary** The role supports pharmaceutical manufacturing operations by assisting in the maintenance, calibration, and reliability of production, laboratory, and utility equipment to ensure safety, quality, and regulatory compliance. The position contributes to process optimization, improvement of OEE and equipment efficiency (e.g., boilers, chillers, HVAC), and supports engineering activities and departmental projects while adhering to GMP, GES standards, Good Documentation Practices, and safety policies. **Key Responsibilities** * Support smooth running of pharmaceutical manufacturing operations, ensuring facilities, equipment, and processes meet safety, quality, regulatory, GES, and industry standards. * Assist in routine maintenance, servicing, and calibration of production, laboratory, and utility equipment to maintain accuracy and efficiency. * Contribute to process optimization initiatives to improve efficiency, productivity, and product quality. * Support improvement of line OEE and equipment efficiencies, including utilities such as boilers, chillers, and HVAC systems. * Learn and support equipment validation activities for manufacturing processes. * Understand and help improve equipment reliability and minimize downtime. * Observe and support planned engineering activities as per defined schedules and plans. * Learn and follow the Engineering quality system, ensuring compliance with GMP, safety, regulatory requirements, and all applicable standards and policies. * Adhere to Good Documentation Practices and safety instructions while working in the area. * Support implementation of departmental objectives and engineering projects. **Education and Skills** * BE (Bachelor of Engineering) – preferably in Engineering or a related discipline. * Basic understanding of pharmaceutical/ manufacturing operations and engineering systems. * Knowledge or willingness to learn GMP, GES standards, and regulatory compliance. * Interest in equipment maintenance, calibra
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