Quality Control Analyst I

BioPharma Consulting JAD Group is seeking a Quality Control Analyst II to join our dynamic team MA. The Quality Control Analyst II will be responsible for conducting various analytical tests, maintaining laboratory equipment, and assisting in method development and validation activities, while adhering to Good Manufacturing Practices (GMP).

Key Responsibilities:

• Perform routine and non-routine analytical and/or microbiological assays, with increasing complexity, to support raw materials, in-process samples, product release, and stability studies, following established SOPs
• Maintain up-to-date training records, adhere to the testing schedule, and ensure the timely completion of all assignments to support the seamless operation of QC activities and uphold the department's commitment to meeting project timelines and quality metrics
• Assist in the maintenance of laboratory equipment and inventory, including the preparation of reagents...

Direct Biologics, LLC is a rapidly growing biotechnology company specializing in advanced regenerative medicine therapies. We are currently seeking a highly skilled and motivated Quality Control Analyst to join our team. As a Senior Quality Control Analyst, you will play a crucial role in ensuring the safety, efficacy, and quality of our late-stage product.

In this role, you will be responsible for conducting comprehensive analysis of our product using state-of-the-art laboratory techniques and complex equipment. You will collaborate closely with cross-functional teams including Research and Development, Process Development, Manufacturing, Quality Assurance, and Regulatory Affairs, with attention on compliance with industry standards and regulatory requirements. Your primary focus will be on method transfers and product characterization, additional tasks include stability and release testing.

Primary Role and Responsibilities:

• Perform day-to-day drug...

Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Quality Control Analyst I 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 Analyst I (RP/ISO) is responsible for conducting routine analysis of materials including: Raw Materials, in-process and finished formulations under general supervision and in accordance with standard...

Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Quality Control Analyst I, that will be primarily focused on wet chemistry, 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 Analyst I (RP/ISO) is responsible for conducting routine analysis of materials including: Raw materials, in-process and finished formulations under...

We are currently seeking qualified candidates for a Quality Assurance/Quality Control (QA/QC) Analyst in LaBella’s Program Management Services Division at our client’s office in Orange, CT. This position will be in the electric and gas utility industry working on key initiatives for a customer service/information technology project. Ideal candidates will have experience in the strictly government regulated, utility industry in New York state. Applicants with experience in the highly regulated pharmaceutical or medical industry would also be considered. The Program Management Services Division at LaBella provides comprehensive management services for complex projects and multi-year capital programs. Project teams are established to provide a customized mix of business consulting, project management, financial control and monitoring, administrative, and technical support services.

Salary Range: $65,000 - $105,000

The specific salary offered may be...

We are currently seeking qualified candidates for a Quality Assurance/Quality Control (QA/QC) Analyst in LaBella’s Program Management Services Division at our client’s office in Rochester, NY. This position will be in the electric and gas utility industry working on key initiatives for a customer service/information technology project. Ideal candidates will have experience in the strictly government regulated, utility industry in New York state. Applicants with experience in the highly regulated pharmaceutical or medical industry would also be considered. The Program Management Services Division at LaBella provides comprehensive management services for complex projects and multi-year capital programs. Project teams are established to provide a customized mix of business consulting, project management, financial control and monitoring, administrative, and technical support services.

Salary Range: $65,000 - $105,000

The specific salary offered may be...

Cambridge Isotope Laboratories, Inc. has an outstanding opportunity to join our GMP Quality Control team as a Quality Control Analyst I based onsite in our Tewksbury, MA headquarters. 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 Analyst I is responsible for conducting routine analysis of GMP/ISO materials including: Raw materials, in-process and finished products under general supervision...