1 Quality Control Analyst I Job in Clayton, NC
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Novo Nordisk is Hiring a Quality Control Analyst I Near Clayton, NC
In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our injectable and oral treatment supply chains. Our legacy Injectable Finished Products (IFP) facility in Clayton, NC is a 457,000 square foot aseptic "fill and finish" site that is responsible for producing innovative, injectable diabetes and obesity treatments. At IFP, you’ll 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 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
The PositionPerform & review analysis of in-process, release & stability samples of API &/or filled product in accordance with cGMP, site & corporate procedures & policies. Transfer of technology & processes in accordance with relevant project plans & timelines.
RelationshipsManager.
Essential Functions
- Ensure accuracy & scientific soundness of lab data
- Ensure environmental compliance
- Support & ensure GMP Laboratory Compliance
- Maintain testing proficiency for methods
- Ensure timeliness of lab results & investigations
- Perform analysis of samples
- Support deviations
- Follow all safety & environmental requirements in the performance of duties
- Other accountabilities, as assigned
Qualifications
- Associate’s degree in science or a relevant field of study from an accredited university required
- Bachelor’s degree in science or a relevant field of study from an accredited university preferred
- One (1) year of work experience in a clinical or industrial/pharmaceutical laboratory preferred
- Ability to author scientific & technical reports is a plus
- Able to perform routine testing per SOP & GMP standards preferred
- Basic level of troubleshooting for laboratory equipment is a plus
- Knowledgeable in GMP & laboratory techniques is a plus
- Demonstrate attention to detail required
- Strong communication skills (verbal & written) preferred
- Skills or knowledge in one of the following disciplines: Chemistry Analysis (HPLC, UPLC, GC, TOC, AA, UV, PH, KF), Microbiology Analysis (Isolator, Sterility, Bacterial Endotoxin testing, Growth Promotion and Microbial Identification, ELISA, BIOBURDEN) or Raw Materials Analysis (Compendial Testing, FTIR, NIR, Titration and UV-Vis) is a plus
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.
Job Summary
Full Time
Pharmaceutical
$57k-76k (estimate)
02/04/2023
07/06/2024
novonordisk-us.com
PLAINSBORO, NJ
200 - 500
1923
Private
DOUG LANGA
$5B - $10B
Pharmaceutical
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The job skills required for Quality Control Analyst I include Analysis, SOP, Chemistry, Microbiology, Troubleshooting, Communication Skills, etc. Having related job skills and expertise will give you an advantage when applying to be a Quality Control Analyst I. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Quality Control Analyst I. Select any job title you are interested in and start to search job requirements.
The following is the career advancement route for Quality Control Analyst I positions, which can be used as a reference in future career path planning. As a Quality Control Analyst I, it can be promoted into senior positions as a Building Inspector, Sr. that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Quality Control Analyst I. You can explore the career advancement for a Quality Control Analyst I below and select your interested title to get hiring information.
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