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Benefits offered by this job
Comprehensive health benefits
401(k) with company contribution
Generous time-off package
Job summary
A global leader in pharmaceutical manufacturing is looking for a Site Quality Head to supervise quality operations at a new Radioligand Therapy manufacturing site. The ideal candidate should have at least 10 years of experience in GMP environments, along with strong leadership and compliance management skills. This role is vital for ensuring the start-up of quality operations, improving safety measures, and maintaining compliance with industry standards. A robust benefits package is included, emphasizing work-life balance.
Qualifications
10 years of experience in a GMP pharmaceutical manufacturing environment.
In-depth knowledge of cGMP and FDA regulations.
Experience applying continuous improvement methods, such as Lean Six Sigma.
Responsibilities
Lead site quality strategy to meet Novartis standards.
Build and develop the Quality team.
Drive plant start-up and expansions ensuring compliance.
Skills
Business Acumen
Collaboration
Communication Skills
Problem Solving Skills
Leadership
Education
Bachelor's degree in life sciences or a related scientific discipline
Job description
A global leader in pharmaceutical manufacturing is looking for a Site Quality Head to supervise quality operations at a new Radioligand Therapy manufacturing site. The ideal candidate should have at least 10 years of experience in GMP environments, along with strong leadership and compliance management skills. This role is vital for ensuring the start-up of quality operations, improving safety measures, and maintaining compliance with industry standards. A robust benefits package is included, emphasizing work-life balance.