Senior Project Manager

Quanta part of QCS Staffing; London; On-site; GBP 40,000 - 60,000; Full time

Job summary

A leading clinical staffing company in London is seeking a QA professional to ensure compliance with GMP by reviewing clinical batch records and approving data packs. The role requires excellent communication skills, issue resolution management, and the ability to work independently. Existing experience in a QA role in a GMP environment is essential. This position offers the opportunity to collaborate closely with global functions in the clinical supply chain.

Qualifications

• Experience in a QA role in a GMP environment.

Responsibilities

• Final review of clinical batch records to ensure compliance with GMP.
• Compile and approve data packs for final release.
• Work closely with global functions supporting the clinical supply chain.

Skills

Excellent communication skills

Issue resolution

Ability to work with minimal supervision

Job description

Responsibilities

• The final review of clinical batch records to ensure compliance with GMP and conformance with regulatory filings.
• Compilation and approval data packs and presentation to the QP for final release.
• Work closely with global functions supporting the clinical supply chain, as well as clinical manufacturing sites internally and externally.

Qualifications

• Excellent communication skills
• An ability to manage issue resolution
• Confidence to work with minimal supervision
• Existing experience in a QA role in a GMP environment