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An established industry player is seeking dedicated individuals to support critical manufacturing processes in a state-of-the-art facility. This role offers the chance to contribute to life-saving treatments while adhering to strict quality regulations. You will engage in various essential functions, including routine documentation, process improvements, and product testing. With a strong emphasis on mentorship and career growth, this position provides a supportive environment for professional development. Join a company committed to inclusivity and excellence, and help make a difference in the healthcare industry.
About the Department
Site New Hampshire, located in West Lebanon, is where Novo Nordisk’s life-saving treatments are produced. Our manufacturing facility supplies a global market with hemophilia and growth hormone products, as well as innovative new medications.
What we offer you:
At Novo Nordisk, we provide opportunities, resources, and mentorship to help you grow your career. Are you ready to realize your potential?
The Position
This role primarily supports manufacturing processes in the designated area, requiring strict adherence to cGMPs, established practices, procedures, and compliance with quality regulations and guidelines.
The Front End Day Schedule
Relationships
Reports to: Supervisor of Manufacturing
Number of subordinates: n/a
Essential Functions
Qualifications
Physical Requirements
Up to 10% overnight travel. Ability to perform physical activities such as climbing, standing, lifting up to 10 pounds, and working in environments with noise, chemicals, and moving parts. Visual and communication skills required.
We are committed to inclusive recruitment and equal opportunity for all applicants.
At Novo Nordisk, we aim to be the best company for the world, fostering a diverse and inclusive culture. We are an equal opportunity employer. For accommodations during the application process, contact us at 1-855-411-5290.