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Biotech Quality Control Jobs in Michigan (NOW HIRING)

QA Associate (Part Time)

Kalamazoo, MI ยท On-site

$19 - $20/hr

Work closely with Manufacturing, Packaging, Warehouse, and Quality Control departments to resolve ... biotechnology, medical device, food, or other regulated manufacturing environment preferred

... control, and document control modules * Serves as the site-level subject matter expert for ... biotech environments * Demonstrated experience with the following: * Managing complex quality ...

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Biotech Quality Control information

See Michigan salary details

$26.6K

$70.9K

$112.9K

How much do biotech quality control jobs pay per year?

As of Aug 14, 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 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 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 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 cities in Michigan are hiring for Biotech Quality Control jobs?

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

Infographic showing various Biotech Quality Control job openings in Michigan as of August 2026, with employment types broken down into 100% Full Time. Highlights an 89% In-person, and 11% Remote job distribution, with an average salary of $70,881 per year, or $34.1 per hour.

QC Microbiologist II

Grand River Aseptic Manufacturing

Grand Rapids, MI โ€ข On-site

$24.50 - $32.25/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 4 days ago


Job description

QC Microbiologist II
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 QC Microbiologist II supports quality control and assurance by assisting the microbiology department with environmental monitoring, water testing, and client specific testing.
The hours for this position are on 1st shift: 6:00 am to 3:00 pm, Monday - Friday.
Non-Negotiable Requirements:
  • Bachelor's degree in Microbiology or a related field.
  • 2-4 years related work experience.
  • Must have proficient computer skills in Microsoft Word, Excel, and Outlook.
  • Knowledge of quality principles and procedures in a pharma, biopharma, and/or biotech manufacturing environment.
  • Strong written and verbal skills.

Preferred Requirements:
  • Experience working in an aseptic manufacturing environment.

Responsibilities Include ( but are not limited to ):
  • Perform sampling and testing of critical utilities (water, pure steam, compressed gasses) to support manufacturing activities.
  • Perform Environmental Monitoring of isolator and supporting areas. Including sampling and reading of media plates.
  • Perform bioburden and endotoxin testing on client specific raw materials, in-process samples, and finished products.
  • Data entry and trending of microbiological testing results
  • Serve as a trainer for tasks performed by Quality Control Microbiology Technicians and Microbiologists.
  • Maintain laboratory equipment - including coordination of calibration and preventative maintenance.
  • Perform daily, weekly, and monthly lab maintenance and supply ordering/stocking.
  • Receive and perform testing on various samples to support validation studies and cleaning verification.
  • Perform general microbiological laboratory tasks including but not limited to; preparation of reagents and standards, performance of growth promotion on media, maintenance of stock organism culture, and preparation isolates for microbial identification.
  • Author Environmental Investigation Reports and Laboratory Investigation Reports.
  • Revise Test Methods and Standard Operating Procedures.
  • Comply with applicable GMPs.
  • Maintain good aseptic conduct in laboratory and cleanroom spaces.
  • Maintain laboratory logbooks and other forms to document proper GMP testing.
  • Perform all job responsibilities in compliance with applicable regulations, standard operating procedures, and industry practice.
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!