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The CAPA Process Analyst leads complex quality investigations, ensuring corrective actions are documented and compliant. Requires CAPA systems experience, a Bachelor's in Life Sciences, and ASQ CQA certification. Effective communication and technical writing are essential.

QC Microbiology Tech role in cancer immunotherapy domain, responsible for quality control testing and environmental monitoring in a GMP-regulated environment. Requires microbiology and environmental monitoring experience, proficiency in MS applications, and ability to work in a fast-paced setting.

Seeking a Quality Control Analyst I in the clinical/scientific domain to perform routine and non-routine chemical testing and analyses using analytical instrumentation. Requires lab experience and skills in compendial testing and wet chemistry. Must communicate effectively and contribute to ...

The Lab Support role requires 2-3 years of lab experience, focusing on analytical testing and data entry in a chemical manufacturing environment. Key responsibilities include conducting tests, measuring properties, and ensuring product quality. A science degree and attention to detail are critical.

The Quality Control Technician role requires 1-2 years of lab and quality control experience. Key responsibilities include performing testing for Lateral Flow, ELISA, and Molecular products, troubleshooting issues, and maintaining GMP/GLP standards. Competencies include knowledge of regulatory ...

The QC Technician I role involves working in a lab environment, performing sample management, coordinating transfers, and supporting QC functions. Requires knowledge of GMP, LIMS, and FDA regulations. Strong attention to detail and communication skills are essential. The position is with a ...

Seeking a Cell Therapy Technician with 1-3 years experience in cGMP manufacturing. Requires troubleshooting skills, equipment operation, and SOP execution. Join a team at a state-of-the-art facility to perform cell processing and ensure compliance. Enthusiasts in innovative immunotherapies ...

The QA Lab Technician will conduct quality control and assurance testing for raw materials, intermediates, and finished products at the Georgia site. Key responsibilities include data evaluation, lab process improvements, and ensuring compliance with ISO 9001 standards. The role requires strong ...

The Regulatory Affairs Coordinator role involves supporting regulatory operations activities requiring strong organizational skills and knowledge of EU and US regulations. Key responsibilities include managing eIFU activities, distribution-related tasks, and developing regulatory strategies. ...

The Regulatory Affairs Coordinator role demands expertise in regulatory operations, particularly in medical device compliance with US FDA and EU MDR regulations. Key responsibilities include supporting eIFU activities, managing regulatory documentation, and executing distribution-related tasks. ...