Description
You will play a vital role in supporting compliance and project activities with accuracy and attention to detail. This role requires working closely with teams across the business to ensure processes run smoothly and meet all compliance standards.
Responsibilities
- Own and drive the function audit universe and audit readiness programme, including Facility and Equipment GEMBA schedules, follow-up actions, and acting as primary contact for inspection readiness activities.
- Define, own and drive continuous improvement programmes and deviations for compliance (including the function Data Integrity plan) and lead daily compliance meetings to generate, review and act on data and frameworks to drive efficiencies and sustain performance.
- Own Quality boards and generate the Monthly Quality pack for technicians/TLs, using recent issues, actions and quality bulletins to challenge existing standards and ways of working to improve compliance, efficiency and robustness.
- Act as the customer for all non–self-delivered projects within the function, ensuring project delivery (equipment, systems and processes) is appropriate for use in production and meets operational requirements, priorities and functional needs.
- Ensure training plans for new equipment and new/updated GMP documentation (SOP, SWI etc.) are fit for purpose, enable technicians to perform their roles compliantly, support seamless integration from installation to steady-state production, and are reviewed periodically on time.
Basic Qualification
- A bachelor’s degree or equivalent experience in a relevant field such as life sciences, business administration, or compliance.
- Experience supporting compliance or project management activities in a regulated environment.
- Strong organisational skills with the ability to manage multiple tasks and deadlines effectively.
- Excellent written and verbal communication skills in English. Proficiency in common office applications such as MS Word, Excel, and PowerPoint.
- Ability to work on-site in the United Kingdom, with hybrid working options considered.
Preferred Qualification
- Previous experience in the pharmaceutical, healthcare, or life sciences industry.
- Familiarity with quality management systems, regulatory requirements or audit processes.
- Experience using project management tools or software.
- Strong problem-solving skills and attention to detail.
- Comfortable working independently and as part of a team.
- Commitment to fostering an inclusive work environment where every voice is heard.
What we offer you You will join a team committed to safety, high standards and practical learning. You will have opportunities to build supervisory and technical skills. You will work with cross-functional partners and contribute to improving processes that matter to patients worldwide.