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.