Associate Director, Quality Operations – NPD & Analytics

Hyper Recruitment Solutions Ltd

United Kingdom

Remote

GBP 90,000 - 130,000

Full time

8 days ago

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Job summary

Hyper Recruitment Solutions Ltd. is seeking an Associate Director - Quality Operations for a leading UK pharmaceutical company.

You will shape quality strategies across NPD and Analytical Development, ensuring compliance and enabling smooth product progression from development to commercialisation. You will lead a global quality operations function, oversee GMP documentation, batch release, audits and continuous improvement, and develop a high-performing Technical Quality team to deliver patient

Qualifications

  • Degree or higher in Chemistry, Pharmacy, Biology or related field.
  • Proven pharmaceutical quality operations experience with GMP systems and manufacturing processes.
  • Eligibility for QP status preferred, with experience supporting analytical development, pre-commercial and commercial activities.

Responsibilities

  • Provide strategic leadership for Quality across New Product Development (NPD) and Analytical Development (AD) functions, ensuring robust quality oversight throughout product lifecycle stages.
  • Support the development and maintenance of comprehensive quality systems, including GMP documentation review and batch release activities.
  • Lead, develop, and coach the Technical Quality team, fostering a culture of continuous improvement and professional growth.
  • Influence quality initiatives, participate in audits, and promote quality by design throughout product and process development.

Skills

Quality leadership
GMP
Audits
Regulatory compliance
Continuous improvement
Team coaching

Education

Degree in Chemistry/Pharmacy/Biology

Job description

Hyper Recruitment Solutions Ltd. is seeking an Associate Director - Quality Operations for a leading UK pharmaceutical company.

You will shape quality strategies across NPD and Analytical Development, ensuring compliance and enabling smooth product progression from development to commercialisation. You will lead a global quality operations function, oversee GMP documentation, batch release, audits and continuous improvement, and develop a high-performing Technical Quality team to deliver patient

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