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Gmp Quality Control Jobs in Michigan (NOW HIRING)

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 ...

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 ...

This individual would be responsible for ensuring that GMP, HACCP, SOPs and other quality ... Monitor and support all QC Program activity such as environmental, foreign material, Allergen ...

... GMP, and all other Quality Assurance programs -Provides training to manufacturing employees on quality control processes, standards, and best practices. -Reports any programming, processing and ...

... GMP, and all other Quality Assurance programs -Provides training to manufacturing employees on quality control processes, standards, and best practices. -Reports any programming, processing and ...

... GMP, and all other Quality Assurance programs -Provides training to manufacturing employees on quality control processes, standards, and best practices. -Reports any programming, processing and ...

Senior Quality Systems Specialist

Lansing, MI · On-site

$75K - $103K/yr

... control, and document control modules * Serves as the site-level subject matter expert for ... Possesses advanced understanding of GMP regulations (FDA, EMA, ICH) and QS principles Great to have.

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Gmp Quality Control information

Is GMP quality control inspection a good career?

GMP quality control inspection is a stable career in the pharmaceutical and biotech industries, focusing on ensuring products meet regulatory standards. It often requires attention to detail, knowledge of Good Manufacturing Practices, and certifications such as GMP training. The role offers opportunities for advancement and consistent employment in regulated environments.

What is the role of quality control in GMP?

In GMP, quality control (QC) is responsible for testing and verifying raw materials, in-process samples, and finished products to ensure they meet specified quality standards. QC helps prevent contaminated or substandard products from reaching consumers and maintains compliance with regulatory requirements through proper documentation and testing procedures.

What is the difference between Gmp Quality Control vs Gmp Quality Assurance?

AspectGmp Quality ControlGmp Quality Assurance
Primary FocusTesting and inspecting products to ensure compliance with standardsDeveloping and maintaining quality systems and processes
ResponsibilitiesSampling, testing, and documenting product qualityAuditing, process validation, and quality system oversight
CertificationsGMP training, laboratory skillsGMP knowledge, quality management system training
Work EnvironmentLaboratories, manufacturing sitesQuality departments, compliance offices

Gmp Quality Control focuses on testing products to verify they meet quality standards, while Gmp Quality Assurance involves establishing and maintaining systems to prevent defects. Both roles are essential in ensuring product safety and compliance in the pharmaceutical and biotech industries.

Is GMP Quality Control a good career?

GMP Quality Control is a vital role in the pharmaceutical and biotech industries, focusing on ensuring products meet regulatory standards through testing and documentation. It often requires attention to detail, knowledge of Good Manufacturing Practices, and certifications such as GMP training. The career offers stability, opportunities for advancement, and the chance to work in regulated environments that prioritize quality and safety.

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

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

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

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

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 4 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