Manufacturing Engineer – Production Operations

About the role

GSK is seeking a Manufacturing Engineer to join its global production environment. You will help extend the scope and effectiveness of site operational programs while ensuring alignment with GSK’s quality and manufacturing system requirements for pharmaceutical, OTC, and medical device products.

Key responsibilities

• Support alignment with GSK Quality and manufacturing system requirements across all product lines.
• Drive compliance activities including training, CAPA, root‑cause analysis, non‑conformance reporting, audits, calibration verification, SOP maintenance, and quality checks.
• Assist in extending the effectiveness of site operational programs and continuous improvement initiatives.

Required profile

• Bachelor’s degree or equivalent experience.
• Minimum 2 years of experience in a cGMP environment.
• Experience in a compliance or quality role.
• Preferred: experience assessing individual and team performance, auditing experience, strong presentation and facilitation skills.

Required skills

• cGMP knowledge
• CAPA management
• Root cause analysis
• Audit execution
• Calibration verification
• SOP development and maintenance

What we offer

• Opportunity to work in a global biopharma leader.
• Access to best‑in‑class systems and technologies.
• Culture focused on patient impact, innovation, and professional development.