Quality Assurance Change Specialist

Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Quality Assurance Change 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 Assurance Change Specialist assists the Quality Assurance department by leading the various change management programs (Document, Equipment, Facility and Information Technology [IT]), all in support of the Food and Drug Administration regulated cGMP (current Good Manufacturing Practices) and ISO 13485 (International Standards Organization) programs.
Responsibilities
Initiates all change plans and assign the appropriate teams for review and approval
Prepares and maintains manufacturing records and SOPs, ensures the proper document format is in place
Monitors custody of change plans to ensure appropriate completion timelines are being met
Creates final original document from completed change control process
Distributes newly approved documents
Maintains hard copy GMP/1SO documentation files
Writes/revises documents as needed
Collaborates with Stakeholders/Subject Matter Experts (SME) in the completion and documentation of equipment, facility and IT change controls
Performs any related work as required
Requirements
Associates Degree in Business/Science or equivalent
Bachelors Degree preferred; equivalent applicable industry experience may be substituted for the degree requirement
Minimum of 5 years of experience working in a chemical manufacturing, biotech or pharmaceutical GMP regulated environment
Advanced knowledge and experience using Microsoft office products including Word, Power Point and Excel
Knowledge of cGMP and ISO documentation control regulations
Experience with Quality Assurance and knowledge and/or experience in ISO 17025, ISO 13485, GMP and ICH Q7A is preferred
Excellent interpersonal, verbal and written communication skills are required
Attention to detail, organizational skills, ability to multitask and follow tasks through to completion
Benefits
CIL and CIS offer a competitive salary and comprehensive benefits including generous paid time off, Long Term Incentives, 6% matching 401K plan and health insurance with no in-network deductible.
CIL is an EEO/Affirmative Action employer.
Learn more about us on our website: 
About Us:
Cambridge Isotope Laboratories, Inc. (CIL) is the world’s leading producer of and stable isotope-labeled compounds. With approximately 750 employees and laboratories in four countries, CIL specializes in the process of labeling biochemical and organic compounds with highly enriched, stable (nonradioactive) isotopes of carbon, hydrogen, nitrogen and oxygen. Our chemists substitute common atoms (e.g., 1H, 12C, 14N, 16O) with rare, highly valued isotopes (e.g., 2H or D, 13C, 15N, 18O) so that the final product can be readily measured or traced using mass spectrometry (MS) or nuclear magnetic resonance (NMR). CIL’s products are utilized in laboratories, medical, government and academic research centers and health care facilities worldwide.
We are proud that CIL products have contributed to medical advancements in cancer research, new-drug development, environmental analysis, and medical diagnostic research. In the past decade, as the fields of proteomics and metabolomics have developed as leading techniques for determining biomarkers for disease presence, progression and the monitoring of therapeutic response, CIL has worked closely with industry leaders and researchers to provide the stable isotope-labeled tools needed for improved quantitation and qualification of complex biological systems.
After decades of research, stable isotopes have found their place in an ever expanding commercial scale applications in pharmaceuticals, semiconductors, flat panel displays as well as other high technology fields specifically with deuterium oxide (D2O) and deuterium gases. Pharmaceutical companies have begun to investigate deuteration of molecules that may provide advantages over their existing nondeuterated counterparts. In addition, increasing research into the potential medical advantages of new deuterated drugs is also occurring. In high technology, deuterated organic molecules and deuterium gas are commonly used in the manufacturing of microelectronics and OLEDs, which contribute to the increased lifetime of the devices.
 
Learn more about us on our website: