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Bio Manufacturing Jobs in Michigan (NOW HIRING)

Groundskeeper

Coldwater, MI

$14.50 - $18.50/hr

Contacts manufacturer for technical assistance when needed and helps place orders for service and ... At times may be requested to transport bio hazard wastes on campus - clinics to hospital ...

Groundskeeper

Coldwater, MI · On-site

$14.50 - $18.50/hr

Contacts manufacturer for technical assistance when needed and helps place orders for service and ... At times may be requested to transport bio hazard wastes on campus - clinics to hospital ...

... Manufacturing markets. ESFM self-performs 80% of all IFM solutions provided to clients. Their ... Collects, transports, and properly disposes of trash and bio-hazardous materials following ...

Team Lead, Production

New Hudson, MI · On-site

$19 - $26/hr

Minimum 3 years manufacturing/operations experience. * Knowledge of and basic skills in lean ... Steps in when operators report in absent, need bio breaks, etc. * Trains Production Associates on ...

Production Team Lead

Hudson, MI · On-site

$17.50 - $24/hr

Minimum 3 years manufacturing/operations experience. * Knowledge of and basic skills in lean ... Steps in when operators report in absent, need bio breaks, etc. * Trains Production Associates on ...

Team Lead, Production

Hudson, MI · On-site

$17.50 - $24/hr

Minimum 3 years manufacturing/operations experience. * Knowledge of and basic skills in lean ... Steps in when operators report in absent, need bio breaks, etc. * Trains Production Associates on ...

Production Team Lead

New Hudson, MI · On-site

$19 - $26/hr

Minimum 3 years manufacturing/operations experience. * Knowledge of and basic skills in lean ... Steps in when operators report in absent, need bio breaks, etc. * Trains Production Associates on ...

Shift Operator

Bangor, MI · On-site

$17 - $22.25/hr

... products manufactured meet the quality and quantity standards set by the organization ... Bio-tech or related experience. PHYSICAL: • Work in cold to hot temperatures; work around dust ...

... manufacturing applications fields preferred. * Supervisory or crew/job project leadership experience preferred. * Familiarity with other facets of bio-pharmaceutical production processes and ...

... manufacturing applications fields preferred. * Supervisory or crew/job project leadership experience preferred. * Familiarity with other facets of bio-pharmaceutical production processes and ...

Biomed Tech

Southfield, MI · On-site

$23.25 - $30.75/hr

Conducting tests; ensuring compliance to codes; following manufacturer's instructions; trouble-shooting and repairing; calling for special service; maintaining equipment inventories; completing test ...

Biomed Tech

Southfield, MI · On-site

$23.25 - $30.75/hr

Conducting tests; ensuring compliance to codes; following manufacturer's instructions; trouble-shooting and repairing; calling for special service; maintaining equipment inventories; completing test ...

Biomed Tech

Southfield, MI · On-site

$23.25 - $30.75/hr

Conducting tests; ensuring compliance to codes; following manufacturer's instructions; trouble-shooting and repairing; calling for special service; maintaining equipment inventories; completing test ...

PRN - Biomedical Technician ll

Kalamazoo, MI · On-site

$23.75 - $31.50/hr

Accordingly, Associates are prohibited from engaging in the unlawful manufacture, sale, distribution, dispensation, possession, or use of any controlled substance or marijuana, or otherwise being ...

Showing results 21-40

Bio Manufacturing information

See Michigan salary details

$30.9K

$69.6K

$98.1K

How much do bio manufacturing jobs pay per year?

As of Aug 8, 2026, the average yearly pay for bio manufacturing in Michigan is $69,592.00, according to ZipRecruiter salary data. Most workers in this role earn between $61,900.00 and $77,600.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in bio manufacturing?

To thrive in Bio Manufacturing, you need a solid background in biology, chemistry, or engineering, often supported by a relevant degree or certification. Familiarity with Good Manufacturing Practices (GMP), bioprocessing equipment, and quality control systems is typically required. Attention to detail, problem-solving abilities, and strong teamwork skills help individuals excel in this environment. These competencies are crucial for ensuring product quality, regulatory compliance, and efficient production in the biotechnology industry.

What are some common challenges faced by professionals working in bio manufacturing, and how can they be addressed?

Professionals in bio manufacturing often encounter challenges such as maintaining strict quality control standards, adapting to rapidly evolving technologies, and ensuring compliance with regulatory requirements. Addressing these challenges involves continuous training, staying updated on industry best practices, and fostering strong communication within cross-functional teams. Many companies also encourage ongoing professional development and provide resources to help employees stay current with regulations and technological advancements.

What is bio manufacturing?

Bio manufacturing, also known as biomanufacturing, is the process of using biological systems like cells or enzymes to produce commercial products such as medicines, vaccines, biofuels, and food ingredients. This field combines biology, engineering, and technology to create products in a controlled and scalable way, often using fermentation or cell culture techniques. Biomanufacturing plays a critical role in the pharmaceutical, biotechnology, and food industries, enabling the production of complex molecules that are difficult to synthesize chemically. Professionals in this field work on developing, optimizing, and scaling up these biological processes to ensure high-quality and cost-effective product output.

What is the difference between Bio Manufacturing vs Bioprocess Technician?

AspectBio ManufacturingBioprocess Technician
CredentialsTypically requires a Bachelor's degree in Biotechnology, Biology, or related fieldOften requires a diploma or associate degree in Biotechnology or related field
Work EnvironmentManufacturing facilities, laboratories, cleanroomsProduction floors, laboratories, cleanrooms
Industry UsageUsed broadly across biotech, pharmaceutical, and biopharmaceutical companiesPrimarily in biotech and pharmaceutical manufacturing
Job FocusOversees entire manufacturing processes, quality control, and compliancePerforms specific tasks in bioprocessing, equipment operation, and sample testing

Bio Manufacturing involves overseeing the entire production process in biotech and pharmaceutical industries, often requiring higher-level degrees and responsibilities. Bioprocess Technicians focus on executing specific bioprocessing tasks, typically with technical diplomas. Both roles work in similar environments but differ in scope and qualifications.

What are popular job titles related to Bio Manufacturing jobs in Michigan? For Bio Manufacturing jobs in Michigan, the most frequently searched job titles are:
Infographic showing various Bio Manufacturing job openings in Michigan as of August 2026, with employment types broken down into 56% Full Time, 22% Part Time, and 22% Contract. Highlights an 100% In-person job distribution, with an average salary of $69,592 per year, or $33.5 per hour.

Sterilization engineer/ Senior Microbiologist

Integrated Resources INC

Grand Rapids, MI • On-site

Full-time

Re-posted 6 days ago


Job description

Company Description

Integrated Resources, Inc is a premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms. IRI has built its reputation on excellent service and integrity since its inception in 1996. Our mission centers on delivering only the best quality talent, the first time and every time. We provide quality resources in four specialty areas: Information Technology (IT), Clinical Research, Rehabilitation Therapy and Nursing.

Job Description

Job Title: Sterilization engineer/ Senior Microbiologist

Location: Grand Rapids, MI
Duration: 12+months (Possibility of extension)
POSITION DESCRIPTION:
Interfaces with diverse cross-functional team members to define and oversee environmental, sterilization and biocompatibility control policies to assure that Healthcare medical devices consistently comply with toxicological, microbiological and particulate contamination control requirements, standards, guidelines and industry practices, both domestic and international.
POSITION RESPONSIBILITIES:

Provides microbial technical expertise during new product development activities, process modification studies and failure investigations regarding microbiological contamination control.

Serves as technical liaison with functional groups, manufacturing sites and sterilization sites.

Evaluates materials and products and recommends appropriate biocompatibility assessment to meet requirements.

Coordinates the biocompatibility testing of new products and materials.

Ensure compliance to Good Manufacturing Practices specific to Buildings, Environmental Control, Cleaning and Sanitation and Personnel Practices.

Assures compliance with all applicable international and domestic regulations and standards by defining policies and conducting regular training and assessments of all manufacturing sites.

Administers the Environmental Monitoring Program for manufacturing areas, in order to provide the necessary information (e.g., viable and non-viable particulate counts, product bio-burden, water and surface microbial levels, etc.) to ensure an appropriately controlled environment meeting regulatory expectations and industry standards.

Communicates detailed information regarding required policies and monitoring results to Manufacturing and Quality Assurance Managers.

Establishes trends; recommends revisions to monitoring program and/or manufacturing process controls.

Ensures effective corrective actions are implemented, where necessary.

Reviews and approves plant cleaning and pest/vermin control practices.

Provides microbiological technical expertise to the Facilities department regarding cleaning and contamination control.

Provides microbiological technical expertise to the Purchasing department in the selection and certification of component vendors.

Defines handling and test requirements for microbiological contamination control of vendor-supplied components as well as work-in-process inventory.

Assure timely, accurate and independent evaluation of product performance and compliance to sterilization and microbiology requirements prior to clinical studies or market release.

Support other business units' sterilization sites and microbiology labs, and act as an expert and advisor to drive improvements and changes.

Interface with validation teams and customers to determine sterilization needs.

Provides statistical support by leading creation of sterilization related metrics for improvement purposes.

Support Regulatory Affairs and other departments by providing reliability input in the evaluation of sterilization controls.

Manages EO Sterilization Validations, Out of Tolerance Investigations, Bacterial Endotoxin Testing.

Capable of working and leading cross functional team's providing microbiological and sterilization expertise.

Must have excellent knowledge of Microsoft word and excel. Statistical analysis a plus. Proficient report writing.

Basic Qualifications:
EDUCATION:

Bachelor of Science degree in Microbiology or related technical discipline.
YEARS OF EXPERIENCE

5+ year's industrial microbiology experience in the Medical Device or Pharmaceutical industry.
SPECIALIZED KNOWLEDGE REQUIRED

thorough familiarity with FDA, EU and other international regulations, standards and guidelines covering sterilization and microbial contamination control in the manufacture of sterile medical devices.

Solid understanding of different types of sterilization methods (EtO, gamma, steam, etc.) including processes and equipment.

Proven leadership and knowledge in international and national standards such as AAMI/ANSI standards, E-Beam, ISO 17665 (Steam), 14160 (Liquid), 11137 (Radiation), 11135 (EtO) and others as applicable (i.e. EN).

Proven management and interpersonal skills.

Excellent organizational and judgment skills.

Ability to maintain and generate accurate records.

Additional Information

Thanks & Regards,
Seema Chawhan
Clinical Recruiter
Integrated Resources, Inc.
IT Life Sciences Allied Healthcare CRO
Certified MBE |GSA - Schedule 66 I GSA - Schedule 621I
DIRECT # - 732-844-8724
Email id - seema @irionline.com| www.irionline.com
LinkedIn: https://in.linkedin.com/in/seemachawhan
Gold Seal JCAHO Certified for Health Care Staffing
"INC 5000's FASTEST GROWING, PRIVATELY HELD COMPANIES" (8th Year in a Row)


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About Integrated Resources

Sourced by ZipRecruiter

Integrated Resources Inc (IRI), based in Edison, NJ, US, is an esteemed player in the staffing solutions industry with a credible presence on their official website irionline.com. Notably, IRI provides a range of professional staffing services including contract, contract-to-hire, and direct hire solutions to a wide spectrum of industries such as healthcare, life sciences, manufacturing, financial, insurance, and others. Since its inception, IRI has been committed to delivering top-talent and optimum solutions to meet its clients' diverse needs.

Industry

Recruiting and staffing services

Company size

51 - 200 Employees

Headquarters location

Edison, NJ, US

Year founded

1996