Quality Control Technician II - Environmental Monitoring API
Quality Control Technician II - Environmental Monitoring API
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
Not Disclosed
Salary Not Disclosed
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
Performs environmental monitoring of classified areas & performs clean utility sampling of process air nitrogen & water systems in accordance with cGMP NNPILP & corporate policies.
Relationships
Reports to Manager Environmental Monitoring.
Essential Functions
- Perform environmental monitoring & clean utility & gaseous utility sampling
- Assists with planning of EM PV activities
- Transition samples to QC Laboratory
- Assists in the Inoculation Process
- Assists in the Inoculation Process
- Performs & documents all work in accordance with GMP site & corporate procedures & policies
- Maintains a safe working environment & ensures compliance with all safety & environmental procedures & regulations
- Other tasks & responsibilities as assigned
Physical Requirements
Occasionally moves equipment &/or supplies weighing up to 33 pounds within the facility. Routinely operates & inspects manufacturing equipment using hands. Must be ability to be on feet for up to a 12-hour shift. Must be ability to gown correctly. Constantly positions oneself to transfer materials within manufacturing environment. Frequently moves about building(s) to access other personnel & operational areas. Corrected vision to 20/30 &/or ability to pass vision screening assessment necessary to procure motorized vehicle license. Occasionally ascends/descends a ladder to access service equipment. Works atop elevated positions at heights. Occasionally required to secure a motorized vehicle license & operate a motorized vehicle. Occasionally works around odorous &/or hazardous materials. Occasionally performs critical job functions in extremely cold work environments. Occasionally positions oneself within confined spaces for inspection repair & maintenance of equipment. Ability to work in loud noise environments with hearing protection. 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.
Qualifications
- Associates Degree or similar in life sciences biotechnology or related field preferred
- Minimum of two (2) years of experience in the pharmaceutical industry or working in a GMP-regulated environment preferred
- Prior experience working in QC Laboratory &/or classified manufacturing environment preferred preferred
- Demonstrated knowledge & skill operating laboratory testing & sampling equipment using data management systems to collect & document work (e.g. LIMS) preferred
- Ability to communicate technical information & ideas to others preferred
- Good technical writing ability & skills preferred
- Proven ability to plan organize & manage execution of own work coordinate effectively with other team members & adapt work plans based on actual business needs preferred
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.
Required Experience:
IC
Employment Type
Full Time
