ZipRecruiter

Log In

1

Biotech Quality Control Jobs in Michigan (NOW HIRING)

next page

Showing results 1-20

All JobsBiotech Quality Control JobsBiotech Quality Control Jobs in Michigan

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 Jun 10, 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 are the typical daily responsibilities of someone working in Biotech Quality Control?

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 job?

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 the Biotech Quality Control position, and why are they important?

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
QC Microbiology Manager - Facility Control

QC Microbiology Manager - Facility Control

Grand River Aseptic Manufacturing

Grand Rapids, MI • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 24 days ago

Job description

The QC Microbiology Manager - Facility Control
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 Microbiology Manager - Facility Control oversees the QC Microbiologists/technicians performing environmental monitoring, critical utilities testing and client-specific in-process microbiology testing in support of aseptic manufacturing. Duties include, but are not limited to: oversight of technicians performing environmental monitoring and critical utility monitoring, review of microbiology test results, monitoring facility/personnel performance with regards to contamination control, and investigation of environmental and utility out of trend/out of specification results.
Non-Negotiable Requirements:
  • Bachelor's Degree in Life Sciences (Microbiology degree preferred) or a related field, and a minimum of 10-15+ years related work experience.
  • At least 4 years of prior management / leadership experience required.
  • At least 5 years of prior experience in a sterile manufacturing environment required.
  • A thorough understanding of cGMP, FDA guidelines and multinational regulatory standards is required.
  • Knowledge of Quality Control, Contamination Control, and Microbiology principles and procedures in a pharma, biopharma, and/or biotech manufacturing environment.
  • Experience and expertise in aseptic manufacturing of regulated products is required.
  • Must have proficient computer skills in Microsoft Word, Excel and Outlook.

Preferred Requirements:
  • Prior experience interacting with regulatory authorities is preferred.

Responsibilities Include (but are not limited to):
  • Provide leadership to Quality Control associates of various levels. Responsibilities include hiring, managing, motivating, coaching and mentoring.
  • Oversee routine testing on water, utilities, in-process samples, personnel and the environment to detect microorganisms and to obtain information on types and levels of microbial contamination.
  • Determine impact of microorganisms on processes/products and evaluate the effectiveness of contamination control strategies on the manufacturing environment.
  • Communicate the status of microbiological testing and results trending to QA, Manufacturing, Validation and other departments as needed.
  • Draft and review technical investigations, protocols and reports; offer conclusions and recommendations based upon study outcomes.
  • Actively participate in environmental investigations and identify/assess corrective and preventive actions.
  • Draft, review and approve protocols, reports and procedures.
  • Oversee or coordinate micro laboratory capital expense projects as it relates to environmental monitoring and facility control.
  • Establish and maintain good practices with regards to testing processes and data management.
  • Along with technical services team, ensure that trending is performed on a routine basis and that periodic summaries are compiled, maintain laboratory logbooks and other documents to ensure GDP.
  • Along with technical services team, establish and monitor facility control testing strategies for current and future cleanrooms.
  • Develop training requirements, ensure all Microbiology personnel are adequately trained and qualified to perform the assigned job functions.
  • Perform all job responsibilities in compliance with applicable regulations, standard operating procedures, and industry best 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!

Apply