Manager, Quality

Posted One Month Ago
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Wallingford, CT, USA
In-Office
92K-151K Annually
Senior level
Biotech
The Role
Manage Wallingford site Quality Management System activities including document control, training, validations, CAPA, NCMRs, deviations, process improvements, and validation approvals. Lead and develop quality personnel, collaborate on new product/process design, support software validation, and ensure compliance with safety and quality procedures.
Summary Generated by Built In

By joining Bio-Techne, you’ll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide.

Pay Range:

$91,700.00 - $150,800.00

Position Summary:  

Position will manage the Quality Management System activities of Bio-Techne's Wallingford site, including but not limited to document control, training, validations, CAPA, NCMRs and deviations among others. This position will lead the qualification process related to the new processes and process improvements may also assist with the software validation process. 

Key Responsibilities:  

  • Manage personnel in the department providing guidance, tools and conducting performance discussions 

  • Write, review & approve the following as appropriate: SOP, COA, Deviation, & Change Impact Assessment 

  • Lead process to ensure compliance with Wallingford Quality Management System. 

  • Leads process to solve product and process related issues and non-conformances and optimization 

  • Lead process to identify and implement process improvement and optimization.

  • Lead quality management system review and improvement process. 

  • Approval of all new and updated process validations. 

  • Collaborate with development and facilitate new product/process design and validation 

  • Follow guidelines and comply with all company safety, quality, and training procedures and regulations 

  • Perform additional duties as assigned 

QUALIFICATIONS 

Education and Experience: 

  • Bachelor’s degree and 8 or more years of relevant experience 

  • Or, Master’s degree in a related field and 2-5 years of relevant experience 

  • Demonstrated leadership capacity with 3-5 years of formal or informal leadership experience.  

Knowledge, Skills, and Abilities: 

  • Ability to lead a team of various skills levels and background. 

  • Working knowledge of Microsoft Word and Excel is required 

  • Must be able to work in a fast-faced environment where you will be required to prioritize your own work and the work of others to meet various project deadlines 

  • Must be able to analyze data to make effective decisions 

  • Must have good verbal and written communication skills, especially across different groups 

  • Must have strong organizational skills and attention to detail 

  • Must work well independently in an environment that requires strategic decision making 

  • Proficient in planning, organizational, and multi-tasking skills to complete assignments in an efficient manner in a fast-paced environment. 

  • Must be able to effectively train new employees 

  • Must be able to effectively lead new projects, especially across different groups 

  • Must stay informed of current trends and developments in area of expertise ​

Working Conditions: 

  • Work performed in a laboratory and production environment with exposure to chemicals, reagents, and standard lab equipment. 

  • Standard schedule hours with occasional variation depending on production needs. 

  • Onsite work required during standard business hours.  

Physical Requirements: 

  • Ability to stand, walk, and perform repetitive laboratory tasks for extended periods. 

  • Manual dexterity required for laboratory equipment and fine measurement techniques. 

  • Ability to work at a computer for extended periods. 

  • Ability to lift and handle materials weighing 5–20 lbs. 


Why Join Bio-Techne:

  • We offer competitive insurance benefits starting on day one: medical, dental, vision, life, short-term disability, long-term disability, pet, and legal and ID shield.
  • We invest in our employees’ financial futures through 401k plans, an employee stock purchase plan (ESPP), Health Saving Account (HSA), Flexible Spending Account (FSA), and Dependent Care FSA.
  • We empower our employees develop their careers through mentorship, promotional opportunities, training and development, tuition reimbursement, internship programs, and more.
  • We offer employee resource groups, volunteer paid time off, employee events, and charity drives to build a culture of caring and belonging. 
  • We offer an accrued leave policy with paid holidays, paid time off, and paid parental leave.
  • We foster a culture of empowerment and innovation, where employees feel valued and encouraged to bring their new ideas to the table.

Bio-Techne is an E-Verify Employer in the United States.


All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or status as a protected veteran.


To protect the interests of all, Bio-Techne will not accept unsolicited resumes from any source other than a candidate application. Any unsolicited resumes sent to Bio-Techne will be considered Bio-Techne property.


This position requires work authorization that does not now or in the future require sponsorship of a visa for employment authorization in the United States (e.g., H1-B visa, F-1 visa (OPT), TN visa or any other non-immigrant work status). If you require a reasonable accommodation to complete an application, participate in an interview, or take part in any other stage of the recruitment process, please contact [email protected] for assistance.

Skills Required

  • Bachelor's degree and 8 or more years of relevant experience
  • Master's degree in a related field and 2-5 years of relevant experience
  • Demonstrated leadership capacity with 3-5 years of formal or informal leadership experience
  • Experience managing QMS activities (document control, training, validations, CAPA, NCMRs, deviations)
  • Experience with process validation and participation in software validation processes
  • Working knowledge of Microsoft Word and Microsoft Excel
  • Ability to work onsite in a laboratory and production environment (exposure to chemicals, reagents, lab equipment)
  • Strong communication, data analysis, organizational, training, and project leadership skills

Bio-Techne Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Bio-Techne and has not been reviewed or approved by Bio-Techne.

  • Healthcare Strength Medical and dental coverage are often regarded as strong, with core health benefits broadly available across U.S. roles. Day-one eligibility and comprehensive options are described as a relative bright spot even when pay sentiment is mixed.
  • Leave & Time Off Breadth PTO, paid holidays, paid parental leave, and volunteer time are emphasized alongside flexible scheduling. Work-life balance elements are seen as strengths relative to base-pay concerns.
  • Strong & Reliable Incentives Quarterly or semi-annual bonuses and eligibility for annual cash incentives add meaningful upside for many salaried roles. Structured plans such as a Management Incentive Plan reinforce predictability of variable pay.

Bio-Techne Insights

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The Company
HQ: Minneapolis, MN
2,512 Employees
Year Founded: 1981

What We Do

Bio-Techne Corporation (NASDAQ: TECH) is a leading developer and manufacturer of high-quality purified proteins and reagent solutions - notably cytokines and growth factors, antibodies, immunoassays, biologically active small molecule compounds, tissue culture reagents, and cell and gene therapy workflow solutions including T-Cell activation technologies. Bio-Techne’s portfolio also includes protein analysis solutions, sold under the ProteinSimple brand name, that offer researchers efficient and streamlined options for automated Western blot and multiplexed ELISA workflow. These reagent and protein analysis solutions are sold to biomedical researchers, as well as clinical research laboratories, and constitute the Protein Sciences Segment. Bio-Techne also develops and manufactures diagnostic products including FDA-regulated controls, calibrators, blood gas and clinical chemistry controls, and other reagents for OEM and clinical customers. Bio-Techne’s genomic tools include advanced tissue-based in situ hybridization assays (ISH) for research and clinical use, sold under the ACD brand, as well as a portfolio of clinical molecular diagnostic oncology assays including the ExoDx®Prostate (IntelliScore) test (EPI) for prostate cancer diagnosis. These diagnostic and genomic products comprise Bio-Techne’s Diagnostics and Genomics Segment. Bio-Techne products are integral components of scientific investigations into biological processes and molecular diagnostics, revealing the nature, diagnosis, etiology and progression of specific diseases. They aid in drug discovery efforts and provide the means for accurate clinical tests and diagnoses. With thousands of products in its portfolio, Bio-Techne generated approximately $714 million in net sales in fiscal 2019 and has over 2,200 employees worldwide.

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