Associate Director - Quality Operations

ROLE OVERVIEW We are currently looking for an Associate Director
- Quality Operations to join a leading pharmaceutical company based in the UK. This exciting opportunity offers a chance to play a pivotal role in shaping quality strategies across new product development and analytical functions, ensuring regulatory compliance and fostering continuous improvement from early development through commercialisation.

As a key member of the Quality Leadership Team, you will provide expert technical guidance, drive quality initiatives, and support the development of innovative products within a dynamic and fast-paced environment. This role is ideal for a senior quality professional looking to influence quality operations and lead cross-functional teams in a global, pharmaceutical manufacturing organisation.

KEY DUTIES AND RESPONSIBILITIES Your duties as the Associate Director
- Quality Operations will be varied however the key duties and responsibilities are as follows:

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.

As the Associate Director, you will influence quality initiatives, participate in audits, and promote quality by design throughout product and process development.

ROLE REQUIREMENTS To be successful in your application to this exciting role as the Associate Director
- Quality Operations, we are looking to identify the following on your profile and past history:

A Degree or higher level in Chemistry, Pharmacy, Biology or a related field.

Proven pharmaceutical quality operations experience, including knowledge of GMP systems and manufacturing processes.

Eligibility for QP status is preferred, along with experience supporting analytical development, pre-commercial, and commercial activities.

WHAT’S IN IT FOR YOU?

Joining our client means being part of a global leader in innovative pharmaceutical development, where your expertise will directly impact product quality and patient safety. You will have the opportunity to influence strategic quality initiatives, lead a talented team, and develop your leadership skills in a collaborative environment. Additionally, our client offers a competitive package, development opportunities, and a rewarding career path in the science and quality sectors.

Key Words: pharmaceutical / quality / leadership / GMP / NPD / analytical development / regulatory / continuous improvement / team management / strategic influence"Hyper Recruitment Solutions Ltd (HRS) is an Equal Opportunities employer. We welcome applications from anyone who meets the role requirements. HRS exclusively supports the STEM sectors, combining recruitment expertise with scientific knowledge to help you advance your career".