Join Synergy – QC Analyst (Packaging Materials) Opportunity
About Us
Synergy is a leading scientific services provider, partnering with global life science organisations to deliver innovative solutions. Our teams integrate seamlessly into client environments, ensuring compliance, efficiency, and excellence in every project.
The Role
We are currently recruiting a QC Analyst (Packaging Materials) to join our team supporting our client’s Quality Control function at their pharmaceutical manufacturing site in Ware.
This is an excellent opportunity for an enthusiastic scientist looking to develop their career within a GMP-regulated laboratory environment. The successful candidate will be responsible for performing quality control testing of packaging material components used in the manufacture of pharmaceutical products, ensuring materials meet defined quality and regulatory standards.
Key Responsibilities
- Perform quality control testing of packaging material samples using approved analytical methods and specifications.
- Conduct visual inspections, dimensional measurements, and basic analytical testing, including IR analysis.
- Accurately prepare, review, and record analytical data in compliance with GMP and data integrity requirements.
- Assess analytical results against predefined acceptance criteria and support technical investigations where required.
- Support process qualifications, validation activities, and laboratory improvement initiatives.
- Perform laboratory equipment maintenance, calibration, and housekeeping activities.
- Promote safe working practices and maintain compliance with GMP, EHS, COSHH, and site procedures.
- Participate in cross-training activities and provide support across the wider laboratory team.
What We're Looking For
- Degree, HNC/HND, or equivalent qualification in Chemistry, Pharmaceutical Science, Biology, or a related scientific discipline.
- Previous laboratory experience within a pharmaceutical, healthcare, life sciences, or other regulated environment desirable.
- Understanding of GMP requirements and data integrity principles (ALCOA+).
- Strong attention to detail with a commitment to delivering high-quality results.
- Experience following SOPs, work instructions, and laboratory procedures.
- Good organisational, problem-solving, and communication skills.
- Competent user of Microsoft Office and laboratory IT systems.
- Team-oriented approach with a commitment to continuous improvement and customer service excellence.
Why Synergy?
- Competitive hourly rate.
- Opportunity to gain experience within a leading global pharmaceutical organisation.
- Exposure to a GMP-regulated manufacturing and laboratory environment.
- Ongoing training and development.
- Potential for contract extension based on business needs and performance.
- Collaborative and supportive team culture.
Location
Ware, Hertfordshire
Contract
12-Months (with potential extension)
Apply Today
Be part of a team that helps ensure the quality and compliance of pharmaceutical products that positively impact patients worldwide.
Submit your CV via our careers page or contact to learn more about this opportunity.
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