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Quality Control Research Associate Jobs in Michigan

Our mission is to make research possible. That starts by employing a talented and highly qualified ... Currently, we are looking to add a GMP QC Chemist I to the team: Responsibilities and Duties:

Our mission is to make research possible. That starts by employing a talented and highly qualified ... Currently, we are looking to add a GMP QC Chemist I to the team: Responsibilities and Duties

Clinical Research Associate - Oncology - Detroit, MI ICON is a global healthcare intelligence and ... Resolve data queries and drive timely, high-quality data entry * Document site progress and ...

Summary: The Senior Clinical Research Associate (Sr. CRA) is an experienced clinical operations ... This role serves as a key resource to study teams, ensuring high-quality study execution, adherence ...

Clinical Research Associate - Oncology - Detroit, MI ICON is a global healthcare intelligence and ... Resolve data queries and drive timely, high-quality data entry * Document site progress and ...

Showing results 41-60

Quality Control Research Associate information

What does a quality control research associate do?

A Quality Control Research Associate is responsible for ensuring that products, materials, and processes meet established quality standards in industries like pharmaceuticals, biotechnology, and manufacturing. They perform laboratory tests, analyze data, and document results to verify the safety, efficacy, and consistency of products. These professionals also help identify areas for process improvement and may assist in developing new testing protocols. Their work is essential for maintaining compliance with regulatory requirements and ensuring that only high-quality products reach the market.

What are the key skills and qualifications needed to thrive as a quality control research associate, and why are they important?

To thrive as a Quality Control Research Associate, you need a strong background in biology or chemistry, experience with laboratory techniques, and typically a bachelor's degree in a related scientific discipline. Familiarity with analytical instruments such as HPLC, GC, and proficiency in data analysis software, as well as knowledge of industry regulations like GMP, are often required. Attention to detail, critical thinking, and effective communication are vital soft skills for ensuring accuracy and collaborating with team members. These competencies are essential to maintain product quality, comply with regulatory standards, and support the reliability of research outcomes.

What are some common challenges faced by quality control research associates, and how can they be addressed?

Quality Control Research Associates often encounter challenges such as managing tight deadlines while ensuring precise and accurate results, adapting to evolving testing protocols, and troubleshooting unexpected data inconsistencies. To address these challenges, it’s helpful to develop strong organizational skills, maintain clear documentation, and collaborate closely with both laboratory and cross-functional teams. Continuous learning and proactive communication can also help resolve issues quickly and uphold rigorous quality standards.

Is a Quality Control Research Associate a good career?

A Quality Control Research Associate is a valuable role in industries such as pharmaceuticals, manufacturing, and food production, focusing on ensuring product quality and compliance with standards. The position often requires attention to detail, knowledge of testing methods, and familiarity with regulatory guidelines, offering opportunities for career growth and specialization. It can be a stable career with potential advancement into supervisory or analytical roles.

What cities in Michigan are hiring for Quality Control Research Associate jobs?

Cities in Michigan with the most Quality Control Research Associate job openings:

QC Chemist I, GMP

Ann Arbor, MI

Cayman Chemical Company
Biotechnology Research and DevelopmentΒ β€’Β 51 - 200 employees

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 5 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.Β 

Currently, we are looking to add a GMP QC Chemist IΒ 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:Β 

  • 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