An exciting opportunity has become available for an experienced Senior Quality Engineer to join a leading global pharmaceutical manufacturing organisation supporting major engineering and capital projects. Working within a collaborative Quality Engineering team, you'll play a key role providing quality oversight across engineering projects, ensuring GMP compliance while partnering closely with Engineering, Validation and Quality stakeholders.


Key responsibilities include:

• Review and approval of engineering documentation
• Quality oversight of Commissioning & Qualification (C&Q) activities
• Review of validation documentation and stability documentation
• Provide quality guidance throughout engineering project delivery
• Escalate quality issues and recommend appropriate corrective actions
• Support compliance with GMP and regulatory requirements
• Work closely with Engineering and Quality teams on major manufacturing projects

To be successful you'll ideally have:

• Minimum 3 years' experience in Quality Engineering or Quality Assurance within the pharmaceutical industry
• Previous Commissioning & Qualification (C&Q) experience
• Experience reviewing validation documentation
• Strong understanding of GMP and Quality Compliance
• Excellent problem-solving skills
• High attention to detail
• Engineering background or experience working closely with engineering teams
• Sterility Assurance experience will be highly regarded

What's on Offer

• 12-month contract with strong possibility of extension
• Opportunity to work on major pharmaceutical manufacturing projects
• Collaborative and supportive team environment
• Global organisation with excellent systems and processes
• Predominantly onsite role with some flexibility to work from home
• Immediate start available

Please click Appy NOW or contact Jo Turner (Divisional Manager) for a confidential discussion jturner@hpgconnect.com