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About the Department
For more than 100 years, Novo Nordisk has been tackling the unmet medical needs of people living with serious chronic diseases, such as diabetes & obesity. 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 Emerging Technologies - Oral Finished Products facility in Durham, NC is a 194,000 square foot tableting and packaging facility that supports the production of our innovative oral treatments for patients with type 2 diabetes. OFP maintains a curious and pioneering spirit, harmonious with our growing pipeline of new products and emerging technologies.
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 12 weeks 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
Performs quality review & approval of Batch Production Records (BPRs), Change Requests (CR's), Deviations & other documentation (in conjunction with LoB) & QA presence & process confirmation on shop floor. Handles release of raw materials & provides quality oversight, review & approval of validation activities associated with minor changes to existing systems. Performs archiving duties & QA presence & process confirmation on shop floor.
Relationships
Manager, Quality Assurance.
Essential Functions
Ensures site compliance with Regulations, ISO standards, corporate & local SOPs
Reviews & approves documentation for Quality approval – components/raw material, batch records, change control requests, deviations & validation documents
Performs QA presence & process confirmation on shop floor
Participates in project teams as a quality resource
Supports, reviews & approves investigations & root-cause analysis
Participates in process confirmations & Go Look Sees
Evaluates trend & report data for QMRs & APR reports
Other accountabilities, as assigned.
Physical Requirements
Occasionally moves equipment &/or supplies weighing up to 33 pounds. Ability to work in an open office environment with the possibility of frequent distraction. Ability to work the hours necessary to support a 24/7 continuous manufacturing operation. Ability to adjust schedule to work with colleagues in other international time zones. Some roles require ability to work 12-hour shifts or longer, day or night. Ability to travel domestically &/or internationally, as necessary.
Qualifications
Bachelor’s degree in life sciences or related field of study from an accredited university required
With P&O review/agreement, equivalent combination of education & internal NN business/operational experience may be substituted for degree as appropriate
Minimum of three (3) years of QA &/or quality related experience required, preferably in the pharmaceutical or medical device industry
Understanding of cGMP manufacturing & production processes & how to apply required
Understanding of the Batch Review Processes required
Understanding of validation preferred
Understanding of quality management systems required
Understanding of quality oversight & on floor production support required
Knowledge in Quality Management Systems
Demonstrated knowledge of critical controls & input/output requirements for NNPILP processes preferred
Excellent written & verbal communication skills required
Basic computer skills in MS Office, MS Project, PowerPoint, etc. required
Auditing experience with certification a plus
Experience in the use of Six Sigma & LEAN tools a plus
Personal Time Management: Sets goals & prioritizes tasks for own work on short-term basis
Meets deadlines & makes regular progress reports on performance
Keeps track & informs management about fluctuation in workload
Performs well with multi-tasking. Adjust priorities in accordance with changing circumstances
Keeps all relevant people informed of current & future plans
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, we’re 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 1-855-411-5290. This contact is for accommodation requests only and cannot be used to inquire about the status of applications.