Deep expertise in sterile and aseptic manufacturing
Lead site quality organization and gxp functions
This role leads the site quality organization to ensure the highest standards of compliance, product quality, and continuous improvement
Job Summary
This role leads the site quality organization to ensure the highest standards of compliance, product quality, and continuous improvement.
Candidates must have deep expertise in aseptic and sterile manufacturing processes including contamination control strategies and cleanroom operations.
The position offers competitive salary, annual bonus, flexible working schedules, and unlimited learning opportunities within an inclusive environment.
Matching Summary
This role leads the site quality organization to ensure the highest standards of compliance, product quality, and continuous improvement.
Salary
Competitive salary; Annual bonus; Flexible working schedule
Skills & Requirements
Must-have
8+ years pharmaceutical manufacturing experience
Deep expertise in sterile and aseptic manufacturing
Lead site quality organization and GxP functions
Act as Technical Responsible Person (Qualified Person)
Ensure FDA inspection readiness and compliance
Nice-to-have
Pre-approval inspection experience
Strong background in data integrity and eCompliance
Experience building diverse and inclusive teams
Ability to operate in complex ambiguous environments
Key Requirements
Degree in Pharmacy, Chemistry, Microbiology or Life Sciences
Minimum 8 years extensive experience in pharma manufacturing