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Process Quality Manager

Idibu

Slough

Hybrid

GBP 80,000 - 100,000

Full time

Today
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Job summary

A global pharmaceutical company is seeking a Process Quality Manager to assist with quality and compliance policies and support clinical quality systems. The ideal candidate will have extensive experience in Quality Assurance and a relevant scientific degree. This role offers a competitive hourly salary and allows remote work, requiring two days on-site in Slough and three days from home. Applicants must have the right to work in the UK and may require a DBS check.

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 Standard Operating Procedures (SOPs) is essential.

Responsibilities

  • Assist with the creation/revision of quality and compliance policies.
  • Support the Head of Process Quality Excellence in developing clinical quality systems/procedures.
  • Ensure quality and compliance risks are appropriately identified and mitigated.
  • Work with internal and external partners for compliance with relevant regulations.
  • Prepare for audits and inspections for internal and external parties.

Skills

Quality Assurance
GCP and GVP knowledge
Experience in writing SOPs
Collaboration with partners

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 clients site in Slough for 2 days per week with 3 days home working / remote.

Apply :

For more information or to apply for this Process Quality Manager please contact the Key Accounts Team on or email Please quote reference 156 812 .

It is essential that applicants hold entitlement to work in the UK

Please note : This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

Employment Type : Full Time

Experience : years

Vacancy : 1

Hourly Salary Salary : £ 35 - 47

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