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Gmp Jobs in Michigan (NOW HIRING)

Perform routine sampling and GMP analytical testing to support the timely release of raw materials, in-process samples, and finished APIs in accordance with approved specifications and procedures ...

Calibration Lead

Brighton, MI · On-site

$45 - $55/hr

The RoleThe Calibration Lead serves as the primary site resource for coordination of a large-scale GMP calibration program involving 500+ manufacturing, utility, and facility assets. This role is ...

Calibration Lead

Brighton, MI · On-site

$45 - $55/hr

This role is responsible for supporting execution and coordination of a large-scale GMP calibration program, including onsite and offsite calibration activities, instrumentation support, compliance ...

This role is responsible for supporting execution and coordination of a large-scale GMP calibration program, including onsite and offsite calibration activities, instrumentation support, compliance ...

In lieu of a degree, a minimum of fifteen (15) years GMP validation experience in a GMP OR regulated manufacturing or similar environment. * Experience must be inclusive of at least three (3) years ...

Maintenance Technician

Kentwood, MI · On-site

$24 - $40/hr

Knowledge of GMP's and other legal requirements for the food industry. * Perform preventive, predictive, and emergency repairs on your line to ensure your equipment is in proper order. * Assist ...

This role ensures compliance with Good Manufacturing Practices (GMP), maintains accurate production records, and supports safe, efficient, and high-quality manufacturing operations. Requirement/Must ...

Operations Support Specialist

Troy, MI · On-site

$48K - $64K/yr

Operations Support Specialist Support manufacturing, review documentation, ensure GMP compliance, and assist with quality improvements in a biotech environment. Job #136226 Manufacturing Birmingham ...

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Gmp information

See Michigan salary details

$12

$29

$41

How much do gmp jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for gmp in Michigan is $29.01, according to ZipRecruiter salary data. Most workers in this role earn between $15.48 and $38.75 per hour, depending on experience, location, and employer.

What is a Gmp?

A GMP (Good Manufacturing Practice) job typically involves ensuring that products, especially in industries like pharmaceuticals, biotechnology, and food production, are consistently produced and controlled according to quality standards. Employees in GMP roles follow strict guidelines to maintain safety, hygiene, and compliance with regulatory requirements. Common GMP job positions include quality control specialists, manufacturing technicians, and regulatory compliance officers.

What are the typical daily responsibilities of a Gmp specialist in a manufacturing facility?

As a GMP specialist, your day may involve overseeing production processes to ensure compliance with regulatory standards, conducting regular audits, and maintaining detailed documentation of all manufacturing activities. You will likely work closely with quality assurance, production, and engineering teams to identify and rectify any deviations from established protocols. Additionally, you may be responsible for training staff on GMP procedures and supporting investigations into product quality issues. This role requires a proactive approach to problem-solving, a keen eye for detail, and frequent interaction with various departments to maintain product quality and safety.

What are the key skills and qualifications needed to thrive in the Gmp position, and why are they important?

To excel in a GMP (Good Manufacturing Practices) specialist role, individuals typically need a strong background in life sciences, quality control, and regulatory compliance, often requiring a relevant bachelor's degree or industry experience. Familiarity with quality management systems, documentation software, and industry-specific certifications like GMP or Six Sigma is highly valued. Attention to detail, problem-solving abilities, and effective communication are crucial soft skills for this position. These competencies ensure strict adherence to regulatory standards, product safety, and continuous improvement within pharmaceutical or food manufacturing environments.

Are GMP jobs in demand?

GMP (Good Manufacturing Practice) jobs are in demand in the pharmaceutical, biotech, and food manufacturing industries due to strict regulatory requirements. These roles often require knowledge of quality control, compliance, and relevant certifications, and employment opportunities tend to grow with industry expansion and regulatory updates.

What are typical GMP job duties?

GMP (Good Manufacturing Practice) jobs typically involve ensuring manufacturing processes comply with quality standards, including monitoring production, maintaining documentation, and inspecting facilities. Employees may also be responsible for cleaning, equipment calibration, and adhering to safety protocols, often requiring attention to detail and knowledge of regulatory requirements. These roles are common in pharmaceutical, biotech, and food manufacturing environments.

What is a typical day in a GMP job?

A GMP (Good Manufacturing Practice) job typically involves following strict protocols to ensure product quality and safety, including inspecting manufacturing processes, documenting procedures, and maintaining cleanliness in the production environment. Employees often work in shifts, use specialized equipment, and adhere to regulatory standards set by authorities like the FDA. Attention to detail and compliance with safety guidelines are essential components of daily tasks.

What skills are needed for Gmp jobs?

GMP (Good Manufacturing Practice) jobs require strong attention to detail, knowledge of regulatory standards, and good documentation skills. Familiarity with manufacturing processes, quality control, and relevant certifications such as GMP training or quality assurance are also important. Effective communication and the ability to work in a regulated environment are essential for success in GMP roles.

What are popular job titles related to Gmp jobs in Michigan?

For Gmp jobs in Michigan, the most frequently searched job titles are:

What job categories do people searching Gmp jobs in Michigan look for?

The top searched job categories for Gmp jobs in Michigan are:

Infographic showing various Gmp job openings in Michigan as of August 2026, with employment types broken down into 80% Full Time, 11% Part Time, 4% Contract, and 5% Nights. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $60,333 per year, or $29 per hour.

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 17 days ago


Job description

Headquartered in Ann Arbor, Michigan, Cayman Chemical Company supplies scientists worldwide with the resources necessary for advancing human and animal health. We offer a vast product catalog that is constantly growing to meet the needs of our clients. Additionally, we provide service programs that include comprehensive solutions to drive clients’ projects to completion.

Our mission is to make research possible. That starts by employing a talented and highly qualified group of experts that develop the tools to support research scientists. 

Currently, we are looking to add a GMP QC Chemist I to the team:

Responsibilities and Duties:

  • Perform routine sampling and GMP analytical testing to support the timely release of raw materials, in-process samples, and finished APIs in accordance with approved specifications and procedures.
  • Assist with GC and HPLC method development, qualification, and optimization activities for new projects in compliance with GMP requirements.
  • Perform analytical testing to support method validation, transfer, verification, stability studies, and investigational activities (e.g., OOS/OOT), as well as other laboratory projects as assigned.
  • Promptly report all data aberrations to management and participate in supervised investigations.
  • Perform laboratory housekeeping, including glassware cleaning, reagent management, and routine instrument preventive maintenance activities.
  • Maintain complete, legible, accurate, and contemporaneous records of all laboratory activities in notebooks, logbooks, and electronic systems in compliance with GMP requirements and data integrity principles.
  • Perform secondary review of analytical data, calculations, and documentation generated by other analysts to ensure accuracy, completeness, and GMP compliance.
  • Communicate work status and progress to the supervisor on a regular basis.
  • Adhere to laboratory safety procedures and requirements, including proper handling of chemicals and hazardous materials.

Requirements:

  • Education: Bachelor's degree in Chemistry or related field.
  • Experience: 1-3 years of laboratory experience using modern analytical instrumentation, including GC, HPLC, Karl Fischer, FT-IR, and related analytical techniques - experience in a GMP-regulated environment is preferred.
  • Proficiency in HPLC/GC analysis and participation in method development, validation, or transfer activities.
  • Ability to work normal business hours on-site in Ann Arbor, MI.
  • Demonstrate Cayman’s Core Values – Integrity, Collaboration, People, Learning, and Excellence.

What we Provide: 

  • Competitive compensation
  • Medical, dental and vision insurance
  • Generous paid time-off (4 weeks) for vacations, sick and/or personal reasons
  • Over 10 paid holidays per year, including the week of 12/24 through 1/1
  • 401(k) plan
  • Tuition Reimbursement and Student Debt Payment Program
  • Life and disability insurance plans
  • Flexible spending accounts for medical and dependent care (FSA)
  • Fun employee events all year long
  • Flexible work schedules
  • Employee assistance program
  • Casual dress
  • Onsite Gym Facility