Process Quality Manager

CK Group; Slough; Hybrid; GBP 80,000 - 100,000; Full time

Job summary

A global pharmaceutical company is seeking a Process Quality Manager based in Slough. This role involves managing quality compliance policies, supporting process quality excellence, and developing clinical quality procedures. Candidates should have extensive experience in Quality Assurance within a pharmaceutical context and proficiency in GCP audits. The position offers a hybrid model, requiring 2 days onsite and 3 days remote working, with an initial contract duration of 12 months.

Qualifications

• Hold a relevant scientific degree or equivalent experience.
• Extensive experience in Quality Assurance in pharmaceutical settings.
• Hands-on experience in global GCP audits and inspections is a must.

Responsibilities

• Assist with the creation of quality and compliance policies.
• Support the Head of Process Quality Excellence.
• Develop and maintain clinical quality systems.

Skills

Quality Assurance

Audit experience

SOP writing

Collaboration

Education

Relevant scientific degree

Job description

Process Quality Manager

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

Role

• Assist with the creation/revision of appropriate quality and compliance policies
• Support the Head of Process Quality Excellence (HPQE)
• Develop and maintain its clinical quality systems and procedures
• Ensure quality and compliance risks are 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.