Process Validation Specialist: Cell & Gene Therapy 12-Month

QCS Staffing; England; On-site; GBP 60,000 - 80,000; Full time

Job summary

A leading Biopharma client in the UK seeks a Process Validation Specialist for a 12-month contract. The role encompasses leading process validation activities in cell and gene therapy manufacturing. Candidates should have a proven track record in process validation and regulatory compliance, with hands-on experience in authoring necessary documentation. This is an excellent opportunity to contribute to cutting-edge projects while establishing yourself as a vital team member in a dynamic environment.

Qualifications

• Proven track record in process validation and process performance qualification (PPQ).
• Hands-on experience authoring validation documentation.
• Familiarity with regulatory requirements for process validation.

Responsibilities

• Lead and execute process validation activities for cell and gene therapy.
• Develop and author process validation documentation.
• Conduct ancillary validation studies such as hold time verification.

Skills

Process validation

Cell and gene therapy

GMP manufacturing

Validation documentation

Regulatory compliance

Job description

A leading Biopharma client in the UK seeks a Process Validation Specialist for a 12-month contract. The role encompasses leading process validation activities in cell and gene therapy manufacturing. Candidates should have a proven track record in process validation and regulatory compliance, with hands-on experience in authoring necessary documentation. This is an excellent opportunity to contribute to cutting-edge projects while establishing yourself as a vital team member in a dynamic environment.