Quality Document Specialist

Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Quality Control Documentation Specialist, based onsite in our Tewksbury, MA facility.  CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets.  CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years.

The Quality Control Documentation Specialist is responsible for performing the data review for the release of regulated and/or non-regulated materials including raw materials, in-process and finished...

Azzur Group is a premier consulting firm specializing in providing innovative solutions to the life sciences industry. Our expertise in quality assurance ensures that our clients' products, processes, and systems meet the highest standards of quality and regulatory compliance. Join us and contribute to projects that enhance product safety, efficacy, and reliability while working in a dynamic and collaborative environment.

We are seeking a detail-oriented and experienced Quality Assurance Specialist to join our consulting team. The Quality Assurance Specialist will be responsible for ensuring that products and processes comply with regulatory requirements and industry standards. The ideal candidate will have a strong background in quality assurance, excellent analytical skills, and a commitment to maintaining high standards of quality and compliance.

Key Responsibilities:

• Develop, implement, and monitor quality assurance processes and procedures to ensure...

Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Quality Control Documentation Specialist based onsite in our Andover, MA facility.  CIL is the global leading company in a highly technical, extremely fast-growing industry and is a critical supplier to several scientific and high technology markets.  CIL's growing customer base spans academia, pharmaceutical, medical diagnostic and semiconductor industries enabling collaborations with Nobel laureates, industry-leading scientists, and chemists. CIL partners with leading instrument manufacturers as well pioneering research groups that have expertise in product development and drive market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over 40 years.

The Quality Control Documentation Specialist is responsible for performing the data review for the release of regulated and/or non-regulated materials including raw materials, in-process and finished...