Top 46 Quality assurance Jobs in White River Junction, Vt

Sr. QA Specialist - Pharmaceutical Manufacturing
Novo Nordisk —West Lebanon, NH
- Monday to Friday
- Writing skills
- Data analysis skills
- English
Quality Engineer - Manufacturing
Jabil Circuit —Claremont, NH
- Full-time
- Mid-level
- Bachelor's degree
- Training & development
- Commuter assistance
- Health savings account
Quality Technician
The Timken Company —Lebanon, NH
- Schematics
- Computer literacy
- Basic math
- Paid parental leave
- AD&D insurance
Quality Manager
Concepts NREC —White River Junction, VT
- $80,000 - $115,000 a year
- Full-time
- Hybrid work
- 5 years
- English
- US work authorization
- Profit sharing
- AD&D insurance
Quality Assurance Associate
IVEK —North Springfield, VT
- $23 - $27 an hour
- Full-time
- Maintenance
- Mid-level
- 3 years
- Health savings account
- Paid holidays
Quality Control Inspector and Administrator
Creare —Hanover, NH
- $25 - $30 an hour
- Full-time
- Microsoft Access
- Computer literacy
- Mid-level
- Health insurance
- 401(k)
Quick Apply
Quality Technician
Concepts NREC —White River Junction, VT
- $18 - $24 an hour
- Full-time
- ERP systems
- Mid-level
- High school diploma or GED
- Profit sharing
- AD&D insurance
13d
Quality Control Technician
Carroll Concrete —West Lebanon, NH
- From $23 an hour
- Overtime
- Mid-level
- Profit sharing
- Disability insurance
Quick Apply
5d
Inprocess Inspector (Retainers)
The Timken Company —Lebanon, NH
- Mid-level
- High school diploma or GED
- Ability to lift 25 pounds
- Paid parental leave
- AD&D insurance
Senior Quality Technician
Concepts NREC —White River Junction, VT
- $26 - $31 an hour
- Full-time
- 5 years
- High school diploma or GED
- Continuous improvement
- Profit sharing
- AD&D insurance
2h
Metallurgy Inspector
The Timken Company —Lebanon, NH
- Computer literacy
- Basic math
- Mid-level
- Paid parental leave
- AD&D insurance
Quality Technician
ImageTek Mfg., Inc. —North Springfield, VT
- $21 - $31 an hour
- Full-time
- Ability to walk for extended periods
- Word processing
- Mid-level
Quick Apply
Quality Manager
Edare —Lebanon, NH
- $115,000 - $140,000 a year
- Urgently hiring
- Engineering
- Senior level
- Communication skills
- Health insurance
- 401(k)
Quick Apply
Roller Inspector
The Timken Company —Lebanon, NH
- Microsoft Outlook
- Computer literacy
- Mid-level
- Paid parental leave
- AD&D insurance
Quality Engineer
The Timken Company —Lebanon, NH
- Engineering
- Microsoft Office
- 3 years
- Paid parental leave
- Paid holidays
Medical Laboratory Technician
Nemaura Medical Inc. —Windsor, VT
- $50 - $55 an hour
- Night shift
- Anatomy knowledge
- Patient monitoring
- Hospital
- Referral program
Quick Apply
5d
Quality Engineer - LED Lighting Products
LEDdynamics —Randolph, VT
- Full-time
- Engineering
- Mid-level
- Office
Quick Apply
Staff Quality Engineer
Hypertherm —Lebanon, NH
- $93,936 - $156,562 a year
- Full-time
- Bachelor of Science
- Travel
- Mentoring
- Profit sharing
- Employee stock ownership plan
Registered Nurse (RN) - Quality and Safety Specialist
Dartmouth-Hitchcock —Lebanon, NH
- $81,723.20 - $130,769.60 a year
- Full-time
- Nursing
- RN License
- Mid-level
- Continuing education credits
- Loan repayment program
Quality Control Coatings Inspector
Canam —Claremont, NH
- Full-time
- English
- Mid-level
- Office
- Opportunities for advancement
Quick Apply

I want to receive the latest job alert for quality assurance in white river junction, vt

By signing in to your account, you agree to SimplyHired's Terms of Service and consent to our Cookie and Privacy Policy.

Explore jobs in more locations

quality assurance jobs near white river junction, vt

Sr. QA Specialist - Pharmaceutical Manufacturing

Novo Nordisk -
West Lebanon, NH

Apply Now

Job Details

Qualifications

Writing skills
English
Bachelor's degree
Stakeholder relationship building
Stakeholder management

Full Job Description

Sr. QA Specialist - Pharmaceutical Manufacturing

Facility: Quality

Location: West Lebanon, NH, US

About the Department

Site New Hampshire, located in West Lebanon, is where Novo Nordisk’s life-saving treatments are brought to life. Our manufacturing facility produces a global supply of our hemophilia and growth hormone product lines, as well as our next generation of cutting-edge medications. It’s not your average production site – it’s a tight-knit, supportive community working together to contribute to a better tomorrow for our patients. Ethics and quality are held in the highest regard, and a patient-focused mindset guides everything we do. We’re looking for individuals who are self-starters with a strong work ethic to join our team. At Novo Nordisk, you will find opportunities, resources and mentorship to grow and build your career. Are you ready to realize your potential?

The Position

This position is responsible for working together with the management team to set future quality direction and supporting the implementation of our ambitious goals by bringing the best practices from other Novo Nordisk sites. The person in this role will be responsible for performing reviews/approving of manufacturing and support documentation and records to certify compliance with in-house specifications/standards and GMP for all site bioloigics produced. This position has QA signature authority on the review of individual batch records, supporting test records and other ancillary support records. Responsibility for developing and coaching QA colleagues as well as supporting manufacturing by being present on the manufacturing floor. This role will help drive implementation of quality improvement projects, and support cross functional projects across the site.

This role is based onsite at our West Lebanon, NH bio-production facility Monday-Friday. Our facility is a 24/7 commercial scale GMP manufacturing facility.

Relationships

Reports to: Sr. Director, QA

Essential Functions

Responsible for training, mentoring and developing other QA colleagues
Responsible for identifying and assessing training needs and delivering training materials and programs, to include training of team members on compliance related issues and other QA related topics
Serve as Good Manufacturing Practice (GMP) expert that responsible for evaluating and improving the effectiveness of training programs
Works closely with Manufacturing and Quality Control to resolve open issues resulting from record reviews, internal audits of the facility, and deviation issues
Informing stakeholders regarding project goals and deliverables
Consult and mentor across business operations and provide specialized knowledge
Reviews and assesses Deviations, including evaluation, tracking, follow-up, and reporting / trending
Reviews and approves Validation Documentation
Reviews and assesses Corrective and Preventive Action Reports
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
Other duties as assigned

Qualifications

Education and Certifications:
- Bachelor’s Degree within a scientific or life science required
- Master’s Degree preferred
Work Experience:
- Bachelor’s Degree with ten (10) years experience required
- Master’s Degree with eight (8) years experience preferred
- Six (6) years of direct QA experience preferred

Knowledge, Skills, and Abilities:
- Excellent written and verbal communication and negotiating skills in English are required
- Strong planning and organization skills, with flexibility for changes in work priorities
- Must be able to exercise judgment within defined practices and policies to determine appropriate action to be taken
- Normally receives no instructions on routine work, and general instructions on new assignments. Determines and develops approach to solutions
- Ability to work on complex Quality projects where analysis of data requires evaluation of identifiable factors
- Ability to train and/or mentor Junior team members in QA Best Practices
- Extensive knowledge in GMP API manufacturing in the pharmaceutical Industry
- Have proven experience with GMP manufacturing in the pharmaceutical industry
- Have good stakeholder management skills and collaboration skills at all levels of the organization

Physical Requirements

Local and International Travel: 0-5%. While performing this job employee work involves sitting most of the time with walking and standing required only occasionally. This position may lift up to 10 pounds occasionally or constantly to lift, carry, push, pull or otherwise move objects. Visual a to perform close activities such as: reading, writing, and analyzing.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and defeating diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.

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.

Apply Now

Refine Your Search

quality assurance jobs in white river junction, vt

Sr. QA Specialist - Pharmaceutical Manufacturing

Quality Engineer - Manufacturing

Quality Technician

Quality Manager

Quality Assurance Associate

Quality Control Inspector and Administrator

Quality Technician

Quality Control Technician

Inprocess Inspector (Retainers)

Senior Quality Technician

Metallurgy Inspector

Quality Technician

Quality Manager

Roller Inspector

Quality Engineer

Medical Laboratory Technician

Quality Engineer - LED Lighting Products

Staff Quality Engineer

Registered Nurse (RN) - Quality and Safety Specialist

Quality Control Coatings Inspector

I want to receive the latest job alert for quality assurance in white river junction, vt

Explore jobs in more locations

Job Seeker Tools

Employer Tools

Browse

Stay Connected