Supervisor, Manufacturing

Posted 2 Days Ago
Be an Early Applicant
Minneapolis, MN, USA
In-Office
70K-115K Annually
Mid level
Biotech
The Role
Lead GMP-regulated production operations for antibodies, proteins, enzymes, and kits. Supervise and train staff, ensure SOP/GMP/ISO compliance, manage filling/capping/labeling/inspection, troubleshoot equipment, maintain batch records and ERP data, drive continuous improvement, support CAPA and new product introductions, and coordinate with cross-functional teams to meet safety, quality, and delivery targets.
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:

$69,800.00 - $114,800.00

Position Summary: 

The Manufacturing Supervisor leads daily operations in a GMP-regulated production environment, supporting the filling, capping, labeling, and inspection of antibodies, proteins, enzymes, and kit components. This role ensures compliance with quality systems while driving safety, efficiency, and on-time delivery. The supervisor oversees team performance, supports technical troubleshooting, and partners cross-functionally to optimize production processes.

Key Responsibilities: 

  • Supervise and develop production staff to meet safety, quality, and throughput targets

  • Ensure adherence to SOPs, GMP/GDP standards, ISO requirements, and documentation practices

  • Oversee product processing, including vial/bottle preparation, aseptic filling (pipetting), capping, labeling, and visual inspection

  • Operate and troubleshoot production equipment (e.g., automated vial torquing and labeling systems)

  • Support laminar flow hood operations and cleanroom gowning procedures

  • Perform or verify production calculations (e.g., volume, concentration, yield)

  • Maintain accurate batch records, inventory transactions, and ERP system data

  • Coordinate priorities with Planning, Quality, Engineering, and Materials teams

  • Investigate deviations, support CAPA activities, and resolve non-conformances

  • Maintain training programs, skills matrices, and cross-training initiatives

  • Monitor and report on production metrics (safety, quality, delivery, efficiency)

  • Participate in continuous improvement efforts (Lean, waste reduction, process optimization)

  • Support new product introductions, process transfers, and lyophilization activities

  • Approve timecards and manage staffing to meet production demands

  • Perform additional duties as assigned

QUALIFICATIONS

Education and Experience:

  • Bachelor’s Degree in Science or Engineering or equivalent experience

  • 3+ years of manufacturing experience in a regulated environment (GMP/ISO preferred)

  • Demonstrated leadership capacity required; previous supervisory experience preferred

  • Working knowledge of manufacturing regulatory compliance requirements

  • Formal continuous improvement training and experience desirable (Lean/ Six Sigma)

Knowledge, Skills, and Abilities:

  • Working knowledge of GMP, GDP, and ISO quality systems

  • Experience with aseptic technique, pipetting, and cleanroom operations

  • Familiarity with laboratory and production equipment, including automated filling, torquing, or labeling systems

  • Ability to perform and verify calculations related to concentrations, dilutions, and volumes

  • Strong troubleshooting and root cause analysis skills

  • Proficiency with ERP/MRP systems and Microsoft Excel

  • Strong attention to detail and documentation accuracy

  • Ability to lead, coach, and communicate effectively in a team environment

  • Ability to manage multiple priorities in a fast-paced production setting

Working Conditions:

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

  • Minimal or no travel required.

Physical Requirements:

  • Ability to lift and handle materials weighing 5–50 lbs.

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

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


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.


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 in Science or Engineering or equivalent experience
  • 3+ years manufacturing experience in a regulated environment (GMP/ISO preferred)
  • Working knowledge of GMP, GDP, and ISO quality systems
  • Demonstrated leadership capacity
  • Previous supervisory experience
  • Formal continuous improvement training and experience (Lean/ Six Sigma)
  • Experience with aseptic technique, pipetting, and cleanroom operations
  • Familiarity with laboratory and production equipment, including automated filling, torquing, or labeling systems
  • Ability to perform and verify calculations related to concentrations, dilutions, and volumes
  • Strong troubleshooting and root cause analysis skills
  • Proficiency with ERP/MRP systems and Microsoft Excel
  • Ability to lift and handle materials weighing 5-50 lbs and perform repetitive lab tasks for extended periods

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

Am I A Good Fit?
beta
Get Personalized Job Insights.
Our AI-powered fit analysis compares your resume with a job listing so you know if your skills & experience align.

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.

Similar Jobs

3M Logo 3M

Manufacturing Supervisor* (Cottage Grove, MN) - 5AM-5PM, 5PM-5AM

Automotive • Hardware • Other • Energy • Industrial
In-Office
Cottage Grove, MN, USA
64670 Employees
96K-117K Annually

3M Logo 3M

Manufacturing Supervisor* (Cottage Grove, MN) - 5AM-5PM, 5PM-5AM

Automotive • Hardware • Other • Energy • Industrial
In-Office
Cottage Grove, MN, USA
64670 Employees
96K-117K Annually

Carfair Composites Logo Carfair Composites

Manufacturing Engineering Supervisor

Automotive • Industrial • Manufacturing
In-Office
St. Cloud, MN, USA
90K-90K Annually
In-Office
Sauk Rapids, MN, USA
762 Employees
80K-135K Annually

Similar Companies Hiring

Formation Bio Thumbnail
Artificial Intelligence • Big Data • Healthtech • Biotech • Pharmaceutical
New York, NY
150 Employees
SOPHiA GENETICS Thumbnail
Software • Healthtech • Biotech • Big Data • Artificial Intelligence
Boston, MA
450 Employees
Pfizer Thumbnail
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
New York, NY
121990 Employees

Sign up now Access later

Create Free Account

Please log in or sign up to report this job.

Create Free Account