London, United Kingdom (Hybrid)
About the Role
What You’ll Do:
- Lead and execute risk-based GMP/GDP audits of CMOs, API manufacturers, laboratories, distributors, service providers and other critical suppliers.
- Support supplier qualification, requalification and ongoing supplier assurance activities across the global supply chain.
- Evaluate supplier quality systems, audit observations, CAPA effectiveness and compliance risks using a risk-based approach.
- Support inspection readiness activities and provide supplier quality expertise during audits and regulatory inspections.
- Apply knowledge of biologics and biosimilars throughout supplier audit planning, quality risk assessment and lifecycle management activities.
- Collaborate with Supply Chain, Regulatory Affairs, Technical Operations, New Product Introduction and Quality teams to maintain compliant outsourced operations.
- Thrive in an entrepreneurial environment, and take accountability for results
- Consistent demonstration and embodiment of company core values: Entrepreneurship, Speed, and Integrity..
About You
Qualifications:
- Degree in Pharmacy, Chemistry, Microbiology, Pharmaceutical Sciences, Life Sciences or a related scientific discipline.
- Formal auditing qualification, auditor training, or demonstrated competency in conducting GxP audits.
- Lead Auditor qualification or advanced audit training (advantageous)
Knowledge, Skills & Experience:
- Extensive pharmaceutical quality auditing experience.
- Experience auditing biologics and/or biosimilar suppliers and manufacturing partners.
- Strong understanding of biologics and biosimilars manufacturing processes, supplier quality systems and associated regulatory expectations.
- Experience supporting supplier qualification, supplier oversight and inspection readiness activities.
- Demonstrated ability to assess supplier quality risks, CAPA effectiveness and compliance gaps using a risk-based approach.
- Good working knowledge of GMP/GDP regulations and quality risk management principles.
- Willingness to undertake regular international travel for supplier audits and quality oversight activities.
- A positive and ‘can-do’ approach, biased towards finding solutions and embracing change.
- Inspired by our values of entrepreneurship, speed and integrity.
Why ADVANZ PHARMA?
A Culture of Empowerment and Belonging:
Flexibility and Support for Your Wellbeing:
Recognition That Inspires:
Global Benefits:
- Global recognition program
- Employee Assistance program
- Birthday leave
- Annual Wellbeing Day leave
- Two days Volunteer leave
- Four weeks working from anywhere
- Compassionate leave
- Long Service Award
Specialist, Quality Audits - Biosimilars in London employer: ADVANZ PHARMA
ADVANZ PHARMA is an exceptional employer, offering a dynamic work environment in Scotland where employees are empowered to make a meaningful impact on patient lives through innovative healthcare solutions. With a strong focus on professional development and a culture that values integrity, speed, and entrepreneurship, team members enjoy opportunities for growth while collaborating with diverse stakeholders in the healthcare sector. The company's commitment to excellence and its global presence provide unique advantages for those looking to advance their careers in the pharmaceutical industry.