Quality Control Associate role at Cook Medical | Life Science Graduates can Applyย
Life Science Job in Quality Control and Laboratory Testing: This role at Cook MyoSite could be an excellent fit for a career in life science. This role is central to supporting quality testing, method development, and compliance in regenerative medicine. Suppose you have a background in Life Sciences, Microbiology, Molecular Biology, or Engineering, and experience in laboratory testing. In that case, this is an excellent opportunity to contribute to cutting-edge medical research and manufacturing.
- Job Position:ย Quality Control Associate I
- Job Type: Full-time, On-site
- Location: Cook MyoSite (part of Cook Medical), USA
About the Company
Cook MyoSite, Inc., part of the Cook Medical family of companies, is focused on advancing regenerative medicine. The organization is investigating its core technologyโautologous muscle-derived cellsโfor the treatment of muscle-related disorders. Joining Cook MyoSite means being part of an innovative team that values integrity, growth, and purpose, while working to make a difference in healthcare worldwide.
Job Description
The Quality Control Associate I role is an exciting Life Science Job that supports method development, sampling, and product testing. This role will aid in developing, maintaining, and executing methods for sampling, testing, evaluating, and approving testing results for products and materials. The role ensures compliance with current Good Manufacturing Practice (cGMP) standards and supports the advancement of regenerative medicine research.
Key Responsibilities
- Perform QC sampling and testing of products/materials for identity, purity, quality, and strength.
- Conduct assays, including DNA isolation, mycoplasma testing, endotoxin detection, desmin analysis, and myogenic differentiation.
- Perform lot testing and document QC-related activities.
- Investigate nonconformance activities and provide additional testing when needed.
- Support method validation, evaluation projects, and quality plan preparation.
- Conduct cell culturing for lot testing and research.
- Maintain side labs, cleanroom environments, and inventory records.
- Ensure compliance with safety, quality, and regulatory standards.
Educational Qualificationsย
Undergraduate degree in Life Sciences, Microbiology, or Molecular Biology
Experience and Skills
- Minimum of 1โ3 years in a laboratory testing environment.
- Basic understanding of cGMP, 21 CFR Part 11, and regulatory requirements for bio/pharma manufacturing.
- Strong analytical, problem-solving, and critical thinking abilities.
- Proficiency in Microsoft Office and general lab equipment.
- Practical verbal, written, and interpersonal communication skills.
- Ability to work independently and collaboratively.
- Trainability and adaptability under changing priorities.
