Current Openings at Badger

W.S. Badger Company, Inc. is an equal opportunity employer, dedicated to the policy of non-discrimination in employment on any basis including gender, race, ethnicity, veteran status, religious affiliation, sexual orientation, age, disability or national origin. We're looking for energetic individuals with strong work habits, skills, and abilities, and a passion for doing the right thing.

Why is Badger such a great place to work?

See a position that you're interested in? Tell us all about yourself in a resume and cover letter. Not finding the perfect fit right now? Send us your information anyway. We'll keep it on file for a future opening.

Apply Online: Click here to fill out the online application. You'll have the option to upload your resume and cover letter.

Apply by Mail: Download our application and mail it in with your resume and cover letter to:
W.S. Badger Company, Human Resources, PO Box 58, Gilsum, NH 03448

No walk-in applications please!


Available Positions - Click each to learn more.

Position Description

The W.S. Badger Company is seeking a Quality Systems Specialist. This fulltime role is responsible for ensuring that the Quality Management System meets Current Good Manufacturing Practices with the intention to improve the product quality and consistency. The Quality Systems Specialist project manages quality investigations, recommends corrective and preventative action plans, and facilitates change control. The Quality Systems Specialist will also serve as a key member of the FDA audit team and is responsible for creating quality improvement plans in response to FDA observations and cGMP consultant recommendations.

Essential Functions:

  • Administer the change control system
  • Author and revise procedures and work instructions
  • Conduct OOS and nonconformance investigations and create CAPAs, as needed
  • Contribute to the improvement of the Quality System by assessing trends in deviation management, complaints, and audit results, and helping to develop corrective actions
  • Serve as member of the audit team during FDA inspections

Experience / Abilities Required:

  • Excellent written communications skills and attention to detail are required
  • Excellent organization and systems thinking
  • 2+ years Quality Assurance experience working in a pharmaceutical manufacturing or packaging facility
  • Experience with Microsoft Office programs required, and experience with QMS programs, and inventory control programs, preferred

Physical Requirements:

Employee must be able to perform essential functions of the position with or without reasonable accommodations.

Interested applicants should submit an online application and specify the position you are applying for. No walk-ins, please.

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