Process Quality Manager

CK Group- Science, Clinical and Technical; Slough; Hybrid; GBP 80,000 - 100,000; Full time

Job summary

A global pharmaceutical company is seeking a Process Quality Manager for an initial 12-month contract. The role involves assisting with quality policies, supporting clinical quality systems, and ensuring compliance with relevant regulations. Candidates should have a scientific degree and extensive experience in Quality Assurance, particularly with GCP. This position requires 2 days on-site work in Slough and 3 days remote, with a salary ranging from £35.20 to £42.08 per hour.

Qualifications

• Extensive experience in Quality Assurance within a pharmaceutical or clinical development setting.
• In depth experience of GCP and GVP, including hands-on experience in global GCP audits and/or inspections.
• Experience in writing SOPs is essential.

Responsibilities

• Assist with the creation/revision of quality and compliance policies.
• Support the Head of Process Quality Excellence in maintaining clinical quality systems.
• Ensure quality and compliance risks are identified and mitigated.

Skills

Quality Assurance experience

GCP compliance knowledge

SOP writing

Education

Relevant scientific degree or equivalent experience

Job description

CK Group are recruiting for a Process Quality Manager to join a global pharmaceutical company on a contract basis initially for 12 months.

Salary: £35.20 ph to £42.08 ph PAYE or £47.92 ph via umbrella

Process Quality Manager Role:

• Assist with the creation/revision of appropriate quality and compliance policies
• Support the Head of Process Quality Excellence (HPQE) in developing and maintaining its clinical quality systems/procedures
• Ensure quality and compliance risks are appropriately identified and mitigated
• Work in collaboration with internal and external strategic partners to ensure compliance with International Council for Harmonisation of Technical Requirements for Pharmaceutical for Human Use (ICH) GCP, GLP, PV and relevant local and international regulations
• Represent or ensure representation, including preparation during audits/inspections for onsite internal and external parties

Your Background:

• Hold a relevant scientific degree or have equivalent working experience
• Extensive experience in Quality Assurance within a pharmaceutical or clinical development setting
• In depth experience of GCP and GVP, including hands on experience in global GCP audits and/or inspections
• Experience in writing SOPs is essential

Company:

Our client is a global biopharmaceutical company focused on creating value for people living with severe diseases in immunology and neurology now and into the future.

Location:

This role is based at our client's site in Slough for 2 days per week, with 3 days home working/remote.

Please note that applicants must hold entitlement to work in the UK. This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

CK Group is an equal opportunities employer and welcomes applications from all qualified candidates.