QA Specialist

Cypartners; Stevenage; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading pharmaceutical company in Stevenage is seeking a QA Specialist for a 6-month contract. The role involves supporting medicine release, ensuring compliance and quality, and participating in audits. Ideal candidates have a BSc in a scientific discipline and experience in GMP environments. This position offers a chance to grow within a dynamic quality assurance team.

Qualifications

• Experience working in a GMP-regulated environment.
• Strong understanding of laboratory testing and pharmaceutical manufacturing processes.
• Laboratory experience is an advantage but not essential.

Responsibilities

• Reviewing, approving and issuing QC data to support timely batch release.
• Providing coaching and support to improve Right First Time (RFT) performance.
• Performing document control activities including controlled printing, reconciliation, and archiving.
• Supporting inspection and audit readiness activities.
• Authoring and reviewing GMP documentation.
• Initiating and participating in quality events such as deviations and change controls.

Skills

Attention to detail

Communication skills

Quality Compliance

Education

BSc in a scientific discipline

Job description

QA Specialist
Location: Stevenage
Salary: £20 p/h
Job Type: 6 Month Contract

Are you passionate about quality and compliance within a scientific environment? Do you have experience working in a GMP-regulated setting and a strong eye for detail? If so, this could be a fantastic opportunity for you to develop your career as a QA Specialist within a biopharmaceutical testing environment.

CY Partners are partnering with a leading pharmaceutical manufacturer to recruit a QA Specialist to support the release of medicines to market. This is an excellent opportunity to join a dynamic quality assurance team in a technically challenging and rewarding role.

Key Responsibilities

• Reviewing, approving and issuing QC data to support timely batch release
• Providing coaching and support to improve Right First Time (RFT) performance
• Performing document control activities including controlled printing, reconciliation, and archiving
• Supporting inspection and audit readiness activities
• Authoring and reviewing GMP documentation
• Initiating and participating in quality events such as deviations and change controls

About You

• A BSc (or equivalent experience) in a scientific discipline
• Experience working in a regulated environment, preferably GMP
• Strong understanding of laboratory testing and/or pharmaceutical manufacturing processes
• Excellent attention to detail with strong documentation and communication skills
• Laboratory experience is advantageous but not essential

This is an exciting opportunity for someone who thrives in a fast-paced, compliance-driven environment and is looking to build or further develop a career in pharmaceutical quality assurance.

If you're ready to take the next step in your QA career and contribute to the delivery of life-changing medicines, we’d love to hear from you.

Apply now with your CV or get in touch with CY Partners for more information.

CY Partners is acting as an Employment Business / Agency in relation to this vacancy.