Process Engineer I - Active Pharmaceutical Ingredients
Process Engineer I - Active Pharmaceutical Ingredients
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1 Vacancy
Job Description
About the Department
At Novo Nordisk we are helping to improve the quality of life for millions of people worldwide. For more than 100 years we have led the way in diabetes care. Being part of Novo Nordisk allows our employees to embark on life-changing careers and the opportunity to help improve the quality of life for millions of people around the world.
In NC we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our injectable and oral treatment supply chains. Our newer Active Pharmaceutical Ingredients (API) facility in Clayton NC sits on 825000 square-feet of state-of-the-art equipment and houses the Fermentation Recovery and Purification in the production of ingredients for Novo Nordisks innovative oral products. At API youll join a global network of manufacturing professionals who are passionate about what they do.
What we offer you:
- Leading pay and annual performance bonus for all positions
- All employees enjoy generous paid time off including 14 paid holidays
- Health Insurance Dental Insurance Vision Insurance effective day one
- Guaranteed 8% 401K contribution plus individual company match option
- Family Focused Benefits including 14weeks paid parental & 6 weeks paid family medical leave
- Free access to Novo Nordisk-marketed pharmaceutical products
- Tuition Assistance
- Life & Disability Insurance
- Employee Referral Awards
At Novo Nordisk you will find opportunities resources and mentorship to help grow and build your career. Are you ready to realize your potential Join Team Novo Nordisk and help us make what matters.
The Position
Provide routine support & troubleshooting for the manufacturing facility. Improve system and equipment reliability for the core processes to meet customer business & regulatory requirements.
Relationships
Reports to Manager or Senior Manager.
Essential Functions
Support validation & verification within area
Ensure quality of equipment and processes
Support process improvement project for assigned area
Support manufacturing operations and provide technical support to the operating facilities to meet business goals
Generate ideas & support implementation for improvement within area
Own self development and partner with manager for clear understanding of development needs for desired career path
Follow all safety & environmental requirements in the performance of duties
Other duties as assigned
Physical Requirements
Moves equipment &/or supplies weighing up to 33 pounds within the facility using various body positions. Routinely operates & inspects manufacturing equipment using hands. Strap & unstrap pallets using hands. Must be able to be on your feet for up to a 12-hour shift. May require corrected vision to 20/20 or 20/25 based on role. May require color vision based on role. Occasionally ascends/descends a ladder. May be required to work at elevated heights. Occasionally works around odorous &/or hazardous materials. May be required to wear latex gloves. May perform critical job functions in extremely cold work environments depending on site. May position oneself within confined spaces for inspection if required of the role. Ability to work in loud noise environments with hearing protection. May be required to secure a motorized vehicle license & operate a motorized vehicle based on the role.
Qualifications
Bachelors Degree in Engineering Science or relevant technical field of study from an accredited university required
May consider an Associates Degree in Engineering Science or relevant technical field of study from an accredited university with three (3) years of engineering or technical experience required preferably in a GMP regulated environment
May consider High School Diploma or equivalent with five (5) years of engineering or technical experience required preferably in a GMP regulated environment
Minimum one (1) year of engineering or technical experience required preferably in a GMP regulated environment
Experience with design of requirements documents a plus
Functional knowledge in assigned area required
Ability to work in a team required
Knowledge about requirements/expectations of regulatory authorities e.g. FDA a plus
Experience with Process Control Systems a plus
Proven ability to establish & maintain networks & facilitate processes that encourage cross organizational knowledge sharing a plus
Ability to provide support for a 24/7 operational business require
We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.
At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees the patients we serve and communities we operate in. Together were life changing.
Novo Nordisk is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race ethnicity color religion sex gender identity sexual orientation national origin disability protected veteran status or any other characteristic protected by local state or federal laws rules or regulations.
If you are interested in applying to Novo Nordisk and need special assistance or an accommodation to apply please call us at 1-. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.
Employment Type
Full Time
