Role / Responsibilities
- Support the manufacture of growth hormone and hemophilia drug materials.
- Perform product manufacturing and manufacturing support activities.
- Complete routine manufacturing documentation.
- Support in-process activities and product development when instructed.
- Incorporate pre-planned process improvements/cost reduction initiatives.
- Perform area equipment and process validations per validation procedures.
- Perform in-process product testing per standard procedures.
- Support manufacturing activities in other departments as instructed.
- Follow GMPs and cleanroom dress/behavior requirements (e.g., hairnet, beard cover, frocks/coveralls, shoe covers, snood, face mask, sterile gloves; prohibited items include food/drink/gum, jewelry, cosmetics, nail acrylics, perfume/cologne, personal cell phones).
- Perform all duties in a compliant and ethical manner; incorporate “Novo Nordisk Way” and 10 Essentials.
Qualifications
- High school diploma or Associate degree (or equivalent) with 3+ years’ relevant manufacturing experience (preferred), or Bachelor’s degree in a science discipline with 0 years’ experience.
- Prefer knowledge of cGMP operations.
- Ability to understand and execute established written instructions.
Benefits (as listed)
- Leading pay and annual performance bonus; 36 paid days off; health/dental/vision insurance; 8% 401(k) contribution plus match option; 14 weeks paid parental leave; free access to Novo Nordisk-marketed pharmaceutical products.
Application instruction
- For application accommodation requests only: call 1-855-411-5290.