R & D Jobs in Bedford, Massachusetts

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

Jobs 1 to 20 of 309
Primary Duties: Reporting to the Clinical Documentation Team Lead, the Clinical Document Specialist is responsible for the management of clinical study records (e.g. clinical Trial Master File) from set up through to final archival, ensuring compliance with company SOPs and process. With a focus on inspection readiness, monitors clinical Trial Master File (TMF) compliance and supports preparatio...
Primary Duties: Reporting to the Clinical Documentation Team Lead, the Clinical Document Manager is responsible for overseeing Clinical Documentation Team (CDT) resource management globally, ensuring effective support for Clinical Development Operation's (CDO) document deliverables. Monitors and supports team compliance with regulatory legislation and Shire policy. Oversees effective outsourcing...
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...
Entegris Job ID 2014-2296 Posted Date 9/8/2014 Job Location US-MA-Billerica Category Engineering & Manufacturing Shift 1st Company Overview and Values: For more than 40 years, Entegris has been a provider of critical products and materials used in advanced high-technology manufacturing. These products and materials are often used to make the building blocks of many of the world's most compl...
Gemini Staffing Consultants, LLC is a leading provider of staffing solutions to the Boston area's Biotech, Pharmaceutical and Medical Device industries with a particular strength in the areas of clinical operations, regulatory affairs and quality assurance. We are a young, progressive company that has seen dramatic year-over-year growth for the past 6+ years with aggressive growth plans in place f...
ImmunoGen, Inc. of Waltham MA is in search of a Sr. Research Associate to join the Bioanalytical Sciences department. The qualified candidate will be responsible for the development and validation of cell-based and immunochemical assays to support product development stability of antibody drug conjugates from late stage research through clinical testing and licensure. Develop and validate GMP com...
ImmunoGen Inc. is in search of a Quality Assurance Specialist responsible for execution of projects in our Good Clinical Practices (GCP) compliance programs. This Specialist will be responsible for ensuring that external and internal laboratories and contract research organizations meet all regulatory requirements. This role will be responsible for: Planning, tracking and performance of GCP audit...
PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, consulting, and medical communications services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed sig...
GCP QA Consultant This position provides operational support for the quality management system within Global Clinical Operations (GCO.) The AD is responsible for assessing the quality measures, and conducting analysis and reporting to support proactive quality management for GCO related processes. The AD will be a Good Clinical Practice (GCP) expert and will provide quality and regulatory guidanc...
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...
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 ...
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...
Company Confidential Lexington, MA, 02421
Synageva BioPharma Corp. JOB DESCRIPTION JOB TITLE Associate Director/Contract Manufacturing REPORTING RELATIONSHIP This position reports to the Vice President of Manufacturing DATE AVAILABLE LOCATION Lexington, MA RESPONSIBILITIES The Associate Director of Manufacturing will support process development, manufacturing and tech transfer activities. The successful candidate will be respons...
Primary Role: • Drives clinical activities of one or more Programs including life cycle management (LCM) and co-leads the development operations team (DOT) • In collaboration with the DOT, defines clinical strategy (clinical development plan, CDP) which is aligned with the Program strategy as defined by the global development team (GDT) • Responsible for the benefit/risk clinical assessment, in...
Primary Duties This position has two primary responsibilities: 1. Global Health Economics , Outcomes Research and Epidemiology (GHEORE) Product (s) support Responsibilities as a member of a Global product team representing and helping execute the GHEORE product strategy. In this capacity you will support the GHEORE product team(s) to which you will be assigned to coordinate and articulate the i...
Job Title: Publications Manager Position Responsibilities The Publications manager will oversee the overall publication strategy and implementation of related activities. Responsibilities include leading the planning, development and execution of publication plans according to and in fulfillment of teams (including field Thought Leaders through Publication Steering Committees) established goals...
Primary Role: Primary duties of this position will include serving as a lead for various technical aspects of the QC areas. Position will provide both subjectmatter expertise as well as technical leadership on activities such as method related projects (ex. method transfers and validations), investigations, quality events, data analysis and trending, key program oversight (ex. reference standard ...
Primary Duties: The Manager of Clinical Trial Transparency (CTT) is responsible for providing oversight and project management-related support of CTT operational activities to ensure accuracy, consistency, and completeness of Shire clinical trial data in support of clinical trial disclosure activities including Global Clinical Trial Registration & Results Disclosure, Clinical Data Sharing, Lay Re...

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