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Biotech Quality Control Jobs in Michigan (NOW HIRING)

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Biotech Quality Control information

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$26.6K

$70.9K

$112.9K

How much do biotech quality control jobs pay per year?

As of Sep 3, 2026, the average yearly pay for biotech quality control in Michigan is $70,881.00, according to ZipRecruiter salary data. Most workers in this role earn between $52,700.00 and $87,200.00 per year, depending on experience, location, and employer.

What is a biotech quality control?

A Biotech Quality Control (QC) job involves ensuring that biological products, processes, and facilities meet regulatory and quality standards. QC professionals conduct testing, analyze data, and document results to verify product safety and efficacy. They work with laboratory techniques such as PCR, HPLC, and microbiological testing. The role is critical in maintaining compliance with industry regulations like GMP and FDA guidelines.

What does a biotech quality control do?

On a daily basis, a Biotech Quality Control professional performs routine testing and analysis of raw materials, intermediates, and finished products to ensure they meet established specifications. This involves preparing samples, operating analytical equipment, maintaining accurate records, and documenting results in compliance with regulatory guidelines. Quality Control staff also collaborate closely with production, quality assurance, and research teams to troubleshoot issues and support process improvements. Regular internal audits and participation in team meetings are common, making communication and teamwork key parts of the job.

What are the key skills and qualifications needed to thrive in biotech quality control?

To excel in Biotech Quality Control, candidates typically need a background in biology, chemistry, or related sciences, with strong knowledge of laboratory techniques and regulatory requirements. Familiarity with laboratory information management systems (LIMS), Good Manufacturing Practices (GMP), and common analytical instruments such as HPLC or PCR is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for this role. These competencies are vital for ensuring that biotech products consistently meet quality and compliance standards essential for patient safety and regulatory approval.

What are the most commonly searched types of Biotech Quality Control jobs in Michigan?

The most popular types of Biotech Quality Control jobs in Michigan are:

What are popular job titles related to Biotech Quality Control jobs in Michigan?

For Biotech Quality Control jobs in Michigan, the most frequently searched job titles are:

What job categories do people searching Biotech Quality Control jobs in Michigan look for?

The top searched job categories for Biotech Quality Control jobs in Michigan are:

What cities in Michigan are hiring for Biotech Quality Control jobs?

Cities in Michigan with the most Biotech Quality Control job openings:

Biotech Quality Control jobs near you
Infographic showing various Biotech Quality Control job openings in Michigan as of August 2026, with employment types broken down into 1% As Needed, 78% Full Time, 15% Part Time, 4% Contract, and 2% Nights. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution, with an average salary of $70,881 per year, or $34.1 per hour.

QC Laboratory Supervisor (2nd shift)

Grand River Aseptic Manufacturing

Grand Rapids, MI • On-site

Full-time, Other

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired today. Applications are no longer accepted.

Job description

QC Laboratory Supervisor (2nd shift)
Agility, Impact, Methodology. Do you exhibit these values and wish to be around others that do too? Do you thrive in fast-paced environments where agility, adaptability, and high standards go hand in hand? Are you driven to make a meaningful impact, whether through your work, your support of others, or your commitment to your community? Are you motivated by a disciplined, science-based approach that ensures consistent excellence, safety, and integrity in everything you do? If these statements resonate with you, Grand River Aseptic Manufacturing (GRAM) welcomes you to apply to join our community of dedicated individuals improving lives every day!
Overview of this Position:
The Quality Control Laboratory Supervisor supports and manages quality systems as they relate to the manufacturing and testing of cGMP drug products.
Hours for this position are 4:00 pm to 12:30 am, Monday - Friday with weekend support necessary depending on the production schedule.
Non-Negotiable Requirements:
  • Bachelor's degree in Chemistry and/or other related discipline (e.g. Biochemistry, Biotechnology) a minimum of 5 years pharmaceutical or testing experience.
  • Must have proficient computer skills in Microsoft Word, Excel, and Outlook.

Preferred Requirements:
  • Knowledge of physical, chemical, and instrumental analysis of raw material, active pharmaceutical ingredients, excipients and finished pharmaceutical products.
  • Experience with various types of laboratory instruments including: HPLC, UHPLC, UPLC, GC, UV-Vis, FTIR, etc.
  • Candidate should understand and have experience with pharmaceutical manufacturing and analytical laboratories in regulated environments under FDA, ICH, and EMA guidelines.

Responsibilities Include (but are not limited to):
  • Manage day to day prioritization of routine, in-process, stability, and finished product work.
  • Supervises lab personnel, including staff performance and creation of staff schedules to ensure over-time/weekend coverage for manufacturing support.
  • Work with management to maintain working schedule of all work flowing through the QC Analytical Lab.
  • Comply with all laboratory safety guidelines, both written and implied. Inform management of any safety concerns.
  • Lead training of all new employees and maintain all training documentation via current system.
  • Support the OOS system, Laboratory Investigations, and assist in any related CAPAs, non-conformances, etc.
  • Work with management to deliver staff performance evaluations, develop individual goals, address performance and progress via routine 1x1 meetings.
  • Oversight of all laboratory chemical and equipment use.
  • Establish and maintain good technique with regards to working in an aseptic environment.
  • Independently author or edit internal test methods and standard operating procedures.
Full job description available during formal interview process.
What Sets GRAM Apart from Other Employers:
BENEFITS starting day 1: Medical, prescription, dental, vision, life insurance, and disability benefits are available to you and your family on your first day of work, with the company paying a portion of the cost! Once eligible for the 401(k) program, all your contributions are immediately 100% vested, and you are immediately vested in GRAM contributions as well. We also offer generous off-shift premiums!
Paid VOLUNTEERISM starting day 1: GRAM encourages giving back to our community by offering 16 hours of paid volunteer time per calendar year!
PAID TIME OFF: You choose how to use this time for your vacation, sick, or mental health needs! PTO: Full-time employees accrue up to 104 hours of paid time off per calendar year, with this amount being prorated your first year. WELLNESS TIME OFF (WTO): In addition to PTO, employees earn 1 hour of wellness time off for every 30 hours worked, to use how you choose.
PAID HOLIDAYS: We offer 10 paid holidays per calendar year with immediate eligibility!
PAY: Depends on Experience and is discussed during the interview process.
If you meet the required criteria listed above, GRAM welcomes you to apply today!

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