R & D Jobs in Bedford, Massachusetts

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454 Bedford, MA R & D jobs found on Monster.

Jobs 1 to 20 of 454
Job Title: Senior QA Specialist/Manager, Quality Assurance Report to: Associate Director, Corporation Quality Assurance Location: Lexington, MA Relocation: Available RESPONSIBILITIES: The Quality Assurance Senior Specialist/Manager will serve as the key interface with corporate personnel and third party partners for day to day support of drug substance and drug product manufacturing, includin...
Primary Duties: The individual will be expected to monitor and provide support for manufacturing operations. Responsibilities will include attending manufacturing morning meeting, daily production data trend review, event response and troubleshooting, batch review, deviation initiation support and manufacturing personnel training. The individual will also be responsible for sampling and/or testing...
Client: Pharmaceutical Company There is more emphasis on the training ability than the PV knowledge. Would accept someone with strong training background and only limited PV exposure or experience. MUST HAVE: - Bachelors Degree - 3+ years conducting training - Some exposure to GCP and Pharmacovigilance - Knowledge of organizational development and adult learning principles and methods Respo...
Merck Millipore is a Life Science leader providing cutting-edge technologies, tools, and services for bioscience research and biopharmaceutical manufacturing. As a strategic partner, we collaborate with customers to confront the world's challenging human health issues. From research through development to production, our scientific expertise and innovative solutions help customers tackle their mos...
New England Research Institutes (NERI) was founded in 1986 and has grown to become a research organization with a global reputation for high-quality research, innovative thinking, and the use of state-of-the-science tools and techniques. NERI continues to be a leader in public health research, clinical trials management, epidemiology, and state of the art media and dissemination research. NERI's ...
Company: Yoh Pharmacovigilance Associate needed for a contract opportunity with Yoh's client located in Cambridge, MA. What You'll Be Doing: - Contribute to the development, production and maintenance of the appropriate tracking and compliance tools, reports, plans, tasks and activities pertaining to the management of the GPE compliance management system. - Perform data entry, deviation closur...
Any combination will do Director GRA Combination Products- Medical Devices ASSOC DIR BIOSURGERY REGULATORY AFFAIRS, * medical device Director, Global Regulatory Affairs Combination Products- Medical Devices Director Global Regulatory Affairs Combination Products and Medical Devices Senior Manager, Global Regulatory Affairs - Medical Devices Joe, 860 889 4141, until 9 pm Eastern, 7 days a wee...
Our client is a top tier company in Cambridge and they are building a surgical core group to support their ever growing in vivo research program. These are newly created, specialized roles and are permanent hires with full benefits in a world class company. Don't miss your chance to join an experienced leadership team in an AAALAC accredited facility supporting a research program that continues to...
RMC is seeking an environmental protection specialist with a bachelor’s degree and 7 years experience or a master’s degree and 3 years experience with environmental impact assessment and NEPA (AICP certification is a plus). The candidate should have background in transportation planning for transit project development and/or city/urban planning. Must have a working knowledge of NEPA, NHPA/Section ...
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries - and growing - we l...
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries - and growing - we l...
Celgene is a global biopharmaceutical company leading the way in medical innovation to help patients live longer, better lives. Our purpose as a company is to discover and develop therapies that will change the course of human health. We value our passion for patients, quest for innovation, spirit of independence and love of challenge. With a presence in more than 70 countries - and growing - we l...
Fermentation Process Development Associate The Process Development Group provides support through the development and optimization of production processes. We work with our R&D and manufacturing colleagues. We are seeking a Research Associate to join our Fermentation Process Development team. This individual will collaborate with Scientists and Process Engineers to design experiments, analyze and...
Senior Scientist – Fermentation Process Development The Process Development Group provides support through the development and optimization of production processes. We work with our Strain Development team and manufacturing colleagues. We are seeking a Fermentation Scientist to join our Process Development team. Responsibilities include all aspects related to development of a robust and scalable ...
Research Assistant or Research Associate Conagen Inc. is a growing Research and Development company located in Bedford, MA. We are currently seeking candidates for a Research Assistant or Research Associate position to assist our research scientists in genetic engineering of industrial microbes such as E. coli and yeast. Duties and Responsibilities • Perform basic lab maintenance tasks such as ...
Automation Specialist Location: Bedford, MA Job Type: Full-time Compensation: Commensurate with skills Overview We are looking for an experienced scientist or engineer with strong expertise in automatic system programing. The candidate will be responsible for operation, maintenance, and protocol development of a liquid handling system (Beckman Biomek). The specialist is also expected to integ...
Primary Role: The Sr Program Manager is experienced in the use of project management tools and principles who can independently manage program activities for two or more CMC teams ensuring that the program stays on track and is within the expected budget and timelines. The senior program manager works closely with the CMC Team Lead to guide the team in developing plans to which bring programs succ...
Primary Role: • Providing leadership and management within CD to provide medical and scientific support for products within assigned therapy area. • Support development and execution of medical & clinical strategy for assigned Shire product(s). • Oversight of study design and data generated, including clinical trial medical monitoring, from Shire sponsored Phase I-IV clinical research programs ...
Primary Duties: Establishes and manages Shire Global Labeling function. Provides regulatory expertise and guidance to Clinical, Pharmacovigilance, Legal, Scientific, Commercial, and other internal stakeholders for successful development of core data sheets and global labeling; formulates and implements regulatory strategies and liaises with regulatory team members to assure that products in devel...
The Clinical Study Manager will assist in the development of observational studies including the development of protocols, informed consent documents, case report forms (CRFs), and CRF guidelines and assists with the development and implementation of study-specific monitoring plan, study tools including communication plan, investigator grants, study budget, study timelines, and study tracking syst...

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