Novo Nordisk is seeking a Sr. QA Specialist for their pharmaceutical manufacturing facility in West Lebanon, NH. The role involves overseeing quality assurance activities, mentoring QA colleagues, and ensuring compliance with GMP standards
Job Summary
This position is responsible for working together with the management team to set future quality direction and supporting the implementation of our ambitious goals by bringing the best practices from other Novo Nordisk sites.
The person in this role will be responsible for performing reviews/approving of manufacturing and support documentation and records to certify compliance with in-house specifications/standards and GMP for all site bioloigics produced.
This role will help drive implementation of quality improvement projects, and support cross functional projects across the site.
Matching Summary
Match Score: 85
Novo Nordisk is seeking a Sr. QA Specialist for their pharmaceutical manufacturing facility in West Lebanon, NH. The role involves overseeing quality assurance activities, mentoring QA colleagues, and ensuring compliance with GMP standards.
Skills & Requirements
Must-have
GMP API manufacturing expertise
Review and approve manufacturing documentation
Develop and coach QA colleagues
Support manufacturing on the floor
Drive quality improvement projects
Nice-to-have
Patient-focused mindset
Self-starter with strong work ethic
Cross-functional project support
Key Requirements
Bachelor's Degree with ten (10) years experience
Master's Degree with eight (8) years experience preferred
Six (6) years of direct QA experience preferred
Bachelor’s Degree within a scientific or life science