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Quality Assurance and Regulatory Affairs Analyst

Throughout 2018, BioTek is celebrating 50 years in business! Over the past five decades, we have evolved as a market leader in detection and imaging instrumentation for life science and drug discovery research. We are recognized globally for our innovative product line and excellent customer service, as well as for being a great place to work!

In this influential position, you will be a member of BioTek’s executive team reporting to the President & CEO in all matters related to Quality and Regulatory Affairs. You will be responsible to develop and implement BioTek quality plans and standards for the design and manufacture of our products. You will also provide detailed quality systems to assure compliance with product design specifications and quality standards including ISO 13485, the IVD Directive/Regulation, the US FDA QSR and international requirements. In-depth knowledge and experience with these standards is critical.

In addition, our ideal candidate will have a bachelor’s or advanced degree in life sciences, ten or more years’ experience in quality management and demonstrated leadership ability. Experience in the medical device industry is strongly preferred.

If you’re interested in becoming a member of the BioTek team, please submit your resume to:

BioTek Instruments, Inc.
Attention: Human Resources P.O. Box 998, Highland Park
Winooski, VT 05404 USA

BioTek is an Equal Opportunity Employer. BioTek does not discriminate on the basis of race, religion, color, sex, gender identity, sexual orientation, age, non-disqualifying physical or mental disability, national origin, veteran status or any other basis covered by appropriate law. All employment is decided on the basis of qualifications, merit, and business need.

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