AbbVieCambridge, 17 mi from Tewksbury (MA)
Job Description
We are seeking an experienced and highly motivated Senior Scientist I to provide scientific, operational, and logistical support for implementing biomarker strategies in multiple neurology and neuropsychiatry, psychiatry clinical...
AbbVieCambridge, 17 mi from Tewksbury (MA)
biologists across the network and be embedded in research project teams in immunology discovery and precision medicine to analyze multi-omic datasets to derive insights into immunological diseases, identify novel therapeutic targets and biomarkers specific...
MindlanceAndover (MA), 6 mi from Tewksbury (MA)
concentration and immunogenicity data to BioMedicine Design Project Leads and other BioTX partners.
Design, develop and implement ligand-binding assays (e.g., MSD, Gyrolab, ELISA) to measure protein concentration of drug and/or biomarker and detect the presence...
Pioneer Data SystemsAndover (MA), 6 mi from Tewksbury (MA)
programs.
Deliver concentration and immunogenicity data to BioMedicine Design Project Leads and other BioTX partners.
Design, develop and implement ligand-binding assays (e.g., MSD, Gyrolab, ELISA) to measure protein concentration of drug and/or biomarker...
Booz Allen HamiltonLexington
Cloud Application Migration Project Manager. As an Application Migration Program Manager, you know how to take advantage of cloud. Experience with project management tools, including Jira, Trello, or Asana. Knowledge of project management methodologies, including Agile, Waterfall, and DevOps.
...
MITREBedford
The successful candidate for this position is a geospatial data scientist who combines a solid theoretical and technical background with the ability to formulate problems, develop and evaluate solutions, and communicate results. Apply a variety of spatial data science techniques to tackle customer c...
MeetBoston, 20 mi from Tewksbury (MA)
first-in-class biologics and innovative treatments.
As a Senior/Principal Scientist in Clinical Biomarkers, you will be a key player in their research efforts to develop therapies that combat neuromuscular disease. You will leverage your extensive...
X4 Life SciencesBoston, 20 mi from Tewksbury (MA)
the pipeline from preclinical stages through clinical development, leveraging their expertise in translational medicine, biomarker development, and oncology/immunology.
Key Responsibilities:
1. Translational Strategy Development: Develop and execute...
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Quality Assurance Associate I
Cambridge Isotope Laboratories, Inc. | Tewksbury | Full-time | apply.workable.com |
Cambridge Isotope Laboratories, Inc. (CIL) is searching for a Quality Assurance Associate I 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 Associate I is responsible for the quality of several new and existing active pharmaceutical ingredients (APIs) and medical device components in a GMP/ISO Environment.
Responsibilities
• Maintenance and management of CIL’s change control process by helping with the initiation of change control, tracking of documents, and final distribution of the approved documents
• Perform room/line clearances, creation of logbooks and controlled forms and form reconciliations
• Review and release of raw materials
• Provide back-up coverage to the stability, training and calibration coordinator
• Support the performance of the other appropriate Quality Assurance functions including document writing/revisions, deviations, CAPA’s, document/data review and other administrative duties as needed
Requirements
• Bachelor's degree in a science and/or quality concentration preferred
• Minimum of 0-2 years of experience with Quality Assurance
• Knowledge and/or experience in ISO 17025, ISO 13485, GMP and ICH Q7A a plus
• Must be detail-oriented with strong organizational skills
• Must possess excellent verbal, written, and interpersonal communication skills and be a team player
• Some travel between facilities is required as this position supports our Tewksbury, MA and Andover, MA locations
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: www.isotope.com
About Us:
Cambridge Isotope Laboratories, Inc. (CIL) is the world’s leading producer of stable isotopes 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: www.isotope.com
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 Associate I is responsible for the quality of several new and existing active pharmaceutical ingredients (APIs) and medical device components in a GMP/ISO Environment.
Responsibilities
• Maintenance and management of CIL’s change control process by helping with the initiation of change control, tracking of documents, and final distribution of the approved documents
• Perform room/line clearances, creation of logbooks and controlled forms and form reconciliations
• Review and release of raw materials
• Provide back-up coverage to the stability, training and calibration coordinator
• Support the performance of the other appropriate Quality Assurance functions including document writing/revisions, deviations, CAPA’s, document/data review and other administrative duties as needed
Requirements
• Bachelor's degree in a science and/or quality concentration preferred
• Minimum of 0-2 years of experience with Quality Assurance
• Knowledge and/or experience in ISO 17025, ISO 13485, GMP and ICH Q7A a plus
• Must be detail-oriented with strong organizational skills
• Must possess excellent verbal, written, and interpersonal communication skills and be a team player
• Some travel between facilities is required as this position supports our Tewksbury, MA and Andover, MA locations
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: www.isotope.com
About Us:
Cambridge Isotope Laboratories, Inc. (CIL) is the world’s leading producer of stable isotopes 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: www.isotope.com