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Global Quality Manager - Commercial Pharma (MAH, GMP/GDP)

Clinigen

Burton upon Trent

On-site

GBP 45,000 - 65,000

Full time

11 days ago

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Job summary

A rapidly growing specialty pharmaceutical company in the UK is seeking a Quality Manager to lead a team and ensure adherence to product quality and compliance standards. The ideal candidate will have a Life Science degree, extensive experience in the pharmaceutical industry, and a strong understanding of GxP regulations. This position includes managing quality documentation, conducting audits, and promoting GMP/GDP compliance. The company offers a comprehensive benefits package including 27 days holiday and pension contributions.

Benefits

27 days holiday plus bank holidays
Discretionary Bonus Scheme
Pension contributions 4.5% matched
Life assurance 4 x annual salary
Flexible Benefits Platform with £25/month Company contribution
Annual salary review
Independent financial advice service
Enhanced Employee Assistance Programme
Shopping discounts with retailers
Long service awards
Recognition scheme & employee of the year awards

Qualifications

  • Extensive experience in the pharmaceutical industry is crucial.
  • Adaptability in changing situations with a proactive approach is required.
  • Ability to work under tight deadlines while maintaining high-quality outputs.

Responsibilities

  • Manage quality and technical activities as a global Marketing Authorisation Holder.
  • Lead relationships with Contract Manufacturing Organisations and quality partners.
  • Oversee quality investigations and manage key quality documentation.

Skills

Life Science knowledge
GMP and GDP knowledge
Leadership and communication skills
Stakeholder management skills
Attention to detail

Education

Life Science degree or equivalent
Job description
A rapidly growing specialty pharmaceutical company in the UK is seeking a Quality Manager to lead a team and ensure adherence to product quality and compliance standards. The ideal candidate will have a Life Science degree, extensive experience in the pharmaceutical industry, and a strong understanding of GxP regulations. This position includes managing quality documentation, conducting audits, and promoting GMP/GDP compliance. The company offers a comprehensive benefits package including 27 days holiday and pension contributions.
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