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Added 1 min ago
Sales Supervisor - King of Prussia
Warby Parker
King of Prussia, PA
● Lead the selling on the floor, front-of-house operations, and team touch-bases when a manager is not present
Added 1 min ago
Program Manager
TT Electronics plc
Perry, OH
Lead Cross-Functional Teams by coordinating activities across Operations, Supply Chain, Engineering, Quality, Finance, and Sales to resolve challenges, capitalize on opportunities, and…
Added 5 mins ago
YO
Member Experience Coordinator
YMCA OF YONKERS INC
Yonkers, NY
- $40,000 to $50,000 USD / year
…Yonkers. This position is responsible for overseeing the daily operations of the Welcome Center, supervising Member Experience Associates, supporting membership growth and retention…
Added 7 mins ago
General Manager
Mammoth Holdings LLC
Spanish Fork, UT
…the culture that drives us to do so each day. As a General Manager, you’ll get an opportunity build and develop the teams that we're known for at Mammoth Holdings. You’ll oversee operations…
Added 10 mins ago
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General Manager
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Chicago, IL
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Lead HVAC Technician
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Home Health Scheduler
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Pharmacy Operations Manager
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Shift Lead
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Shift Lead
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Pharmacy Operations Manager
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ST PETERSBURG, FL
- $22.5 to $35.75 USD / hour
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Added 34 mins ago
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Pharmacy Operations Manager
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ARCADIA, FL
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Closed listing

Bio-Techne

Manager, Quality Control

Devens, MA, United States

$91,700.00 - $150,800.00

This opening has closed.

The original listing is kept below for reference.

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About employer

Job details

Pay: $91,700.00 - $150,800.00
Education: Bachelor’s degree
Posting language: English
Posted: Nov 14, 2026

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Original job description

Archived listing. The details below describe a past opening.

In-person

Devens, MA

Full time

JR102273

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:

The position requires management of the day-to-day operations within the various Quality Control groups (including QC laboratory, Incoming QC). Procedures and processes developed and supported must adhere to FDA cGMP and ISO 13485 Medical Device Requirements. Principal testing types include: blood gas and electrolytes, glucose, co-oximetry, general chemistries, and coagulation.

Responsibilities:

Manage and lead the team, including but not limited to ensuring adequate staffing levels, recruitment, training, development, appraisal, attendance, disciplinary issues, and quick, effective problem resolution that maximizes efficient productivity and delivers a high level of employee engagement.
Oversee daily functions of each department and identify opportunities for improvement
Drive training and development of team members and work closely with department Supervisors to ensure the completion of team and individual goals.
Help supervisors organize and schedule workflow in each functional area (Incoming QC and QC lab) to ensure smooth operation.
Provide direction and support to all QC-related functions.
Align with senior leadership initiatives and support corporate goals for the business.
Maintain a regular ‘on-floor’ presence, regularly adopting GEMBA techniques.
Positively engage with personnel to understand challenges and issues through continuous assessment and implement change where necessary.
Lead/participate in continuous improvement initiatives in line with the vision of the department and the business.
Mentor, motivate, and empower personnel within the team to implement change successfully.
Support senior leadership initiatives and specific site goals.
Partner with Manufacturing, Quality Assurance, Supply Chain, and R&D to resolve product quality issues and support business objectives.
Establish and monitor quality control systems.
Oversee program for the monitoring of temperature-controlled storage areas
Identify critical points in the manufacturing processes where quality checks can be added.
Develop inventory systems for critical lab supplies, reagents, and reference materials.
Participate in New Product Development supporting test methods for new product types.
Develop appropriate sampling plans, test protocols, and quality standards for raw materials, work in process, and finished goods as required for new product development activities
Support new product launch activities, including pilot lots.
Coordinate and oversee instrument acquisition and validation activities
Participate in budgetary review and capital expenditure process for new instrument requests.
Participate in test equipment validation planning, execution and implementation.
Support validation activities related to design changes or technology refresh.
Lead investigation and resolution of Out-of-Specification (OOS), Out-of-Trend (OOT), laboratory deviations, and invalid assay results.
Ensure timely completion and effectiveness of laboratory investigations and associated CAPAs.
Ensure QC operations maintain inspection readiness for FDA, ISO 13485, customer, notified body, and internal audits.
Lead responses to QC-related audit observations and regulatory findings.
Oversee stability testing programs including real-time, accelerated, and in-use stability studies.
Monitor stability trends and support shelf-life assignments and extensions.
Follow company policies and practices as outlined in the Handbook, SOPs and WIs and as well as follows guidelines regarding safety as outlined in the safety program and in accordance to the job functions in the department.
Demonstrates flexibility to support business needs, including occasional extended work hours during investigations, audits, validations, new product launches, or critical business activities.
Willingness to accept changes in work from day-to-day within reasonable and expected boundaries
Perform other duties as assigned.

Qualifications:

Bachelor's degree in Chemistry, Biochemistry, Biology, Clinical Laboratory Science, or related discipline required.
8+ years of laboratory, quality control, or analytical testing experience in a regulated medical device, IVD, biotechnology, or pharmaceutical environment.
Minimum 3-5 years of people leadership experience required.
Demonstrated experience with FDA QSR/QMSR, ISO 13485, and cGMP requirements.
Experience with assay validation, method transfers, statistical analysis, and root cause investigations.
Experience supporting FDA, ISO, customer, or notified body audits preferred.

Minimum Physical Requirements:

Remain seated in a normal position for extended periods of time up to 8 hours
Walk, stand, and move about at various times in the workday
Reach up and out with hands and arms
Talk and hear; verbally express information
Keyboard, 10 keys for extended periods
Repetitive motion; hands
Lift up to 25 pounds and carry at a distance of 10 feet

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 hr@bio-techne.com for assistance.

Bio-Techne empowers researchers in Life Science and Clinical Diagnostics by providing high-quality reagents, instruments, custom manufacturing, and testing services. Our family of brands creates a unique portfolio of products and services.

Science is our passion; it drives us to collaborate, develop, and manufacture award-winning tools that help researchers achieve reproducible and consistent results.

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Jobs in the United States