Sr. QA Specialist - Pharmaceutical Manufacturing
Not Disclosed•Full-TimeOn-site
location_on98, Main Street, West Lebanon, Lebanon, Grafton County, New Hampshire, 03784, United States
About the Department
Site New Hampshire, located in West Lebanon, is where Novo Nordisk's life-saving treatments are brought to life. Our manufacturing facility produces a global supply of our hemophilia and growth hormone product lines, as well as our next generation of cutting-edge medications. It's not your average production site – it's a tight-knit, supportive community working together to contribute to a better tomorrow for our patients. Ethics and quality are held in the highest regard, and a patient-focused mindset guides everything we do.
At Novo Nordisk, you will find opportunities, resources, and mentorship to grow and build your career. Are you ready to realize your potential?
Work location
Work model: On-site
98, Main Street, West Lebanon, Lebanon, Grafton County, New Hampshire, 03784, United States
Lebanon, New Hampshire
Key Responsibilities
- check_circleReview and approve manufacturing documentation and records to ensure GMP compliance
- check_circleExercise QA signature authority on batch records and supporting test records
- check_circleCollaborate with manufacturing and quality control to resolve audit and deviation issues
- check_circleReview and approve validation documentation for manufacturing processes
- check_circleDrive implementation of quality improvement and cross-functional projects
- check_circleTrain, mentor, and develop QA colleagues on compliance and best practices
- check_circleEvaluate, track, and report on deviations and corrective action reports
Requirements
- verifiedBachelor's Degree in scientific or life science
- verified10 years experience with Bachelor's Degree
- verified8 years experience with Master's Degree
- verified6 years direct QA experience preferred
- verifiedExcellent written and verbal communication skills in English
- verifiedExtensive knowledge in GMP API manufacturing
Nice to Have
Master's Degree. Eight (8) years of work experience with a Master's Degree. Six (6) years of direct QA experience.
