1 QC Associate (Technical Writing) Job in West Lebanon, NH
Novo Nordisk is Hiring a QC Associate (Technical Writing) Near West Lebanon, NH
What We Offer You
- Leading pay and annual performance bonus for all positions
- 36 Paid days off including vacation, sick days & company holidays
- Health Insurance, Dental Insurance, Vision Insurance
- Guaranteed 8% 401K contribution plus individual company match option
- 12 weeks Paid Parental Leave
- Free access to Novo Nordisk-marketed pharmaceutical products
The PositionThis position has primary responsibility to support operations for Quality Control at our biologics manufacturing facility. Assists in coordination and execution of process and equipment improvement programs, creates technical reports, reviews completed quality records, generates quality comment and deviation responses and has ability to provide training support. Prior experience as a Technical Writer, or peforming Technical Writing, is preferred for this position. This role will support our QC teams under the direction of the QC Manager.
Relationships
- Reports to: Quality Control Manager
- Number of subordinates with direct/indirect referral: no direct reports
- Liaison between Manufacturing and QC for the coordination of process/equipment improvements, sample testing and data trending/analysis
- Review of completed QC documentation
- Ability to assist with training to support on the QC equipment/processes
- Revise documentation (SOP, forms, reports, notebooks) associated with the testing of in-process/product samples, requiring some direction
- Incorporate pre-planned process improvements and cost reduction projects into QC
- Ability to take on multi-disciplined projects, with minimal supervision
- Functional understanding/application of quality systems with the ability to manage Change Controls
- Support deviation and CAPA investigations and corrective actions
- Support of Health Authority inspections
- Support area equipment validations in accordance with procedures requiring some direction
- Possesses technical and systems knowledge and is able to research information outside of knowledge base
- Has ability to recognize problems and recommend solutions to problems based on technical understanding of testing techniques
- Other duties as assigned
- Performs all job duties and responsibilities in a compliant and ethical manner and in accordance with all applicable healthcare laws, regulations and industry codes
- Incorporates the Novo Nordisk Way and 10 Essentials in all activities and interactions with others
- Education and Certifications:
- High School diploma or equivalent with a minimum of six (6) years relevant manufacturing experience or a Bachelor’s degree or equivalent in a science or engineering discipline with three (3) or more years of experience
- Knowledge, Skills, and Abilities:
- Requires functional understanding of cGMPs, established manufacturing practices and procedures, and compliance with Quality regulations and guidelines
- Ability to understand and execute established written instructions is essential
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.
Job Summary
Full Time
Pharmaceutical
$70k-91k (estimate)
05/21/2024
07/14/2024
novonordisk-us.com
PLAINSBORO, NJ
200 - 500
1923
Private
DOUG LANGA
$5B - $10B
Pharmaceutical
Related Companies
The job skills required for QC Associate (Technical Writing) include Quality Control, Analysis, SOP, Coordination, Process Improvement, etc. Having related job skills and expertise will give you an advantage when applying to be a QC Associate (Technical Writing). That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by QC Associate (Technical Writing). Select any job title you are interested in and start to search job requirements.
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