R & D Jobs in Wellesley, Massachusetts

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489 Wellesley, MA R & D jobs found on Monster.

Jobs 1 to 20 of 489
Senior Clinical Trial Manager/Associate Director, Clinical Trials (NJ, MA, CT) Overview: The Senior Clinical Trial Manager/Associate Director works closely with internal team members and vendors to ensure that assigned clinical trials are conducted per protocol, in a timely fashion and in a manner compliant with SOPs, ICH/GCP/regulatory guidelines, company goals and established study budgets. Th...
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 ...
Sr Manager Global Labeling - Regulatory Affairs Business Unit: Global Development Division: Vaccines & Diagnostics Company/Legal Entity: Novartis Job Reference Code: 148050BR Lead the RA Global Labeling (GL) group for the development and review of NVD vaccine labeling to ensure compliance with regulatory guidelines ranging from the development of reference documents such as Core Data Sheets o...
In this start up role, the Manager, Clinical Trials (Office of Commercialization & Ventures) will work closely with internal staff members and vendors to ensure that assigned clinical trials are conducted per protocol, in a timely fashion and in a manner compliant with all regulatory guidelines, organizational goals and established study budgets. In this exciting venture, The Manager, Clinical Tr...
The Research Assistant (Animal Physiology Core) coordinates and conducts the services for a core physiology laboratory for the evaluation of animal behavior, physiology, and metabolism in rodent models. Responsibilities include: Performs research procedures on mice including but not limited to blood pressure monitoring, body mass composition, hypoxia/hyperoxia experiments, telemetry, behavioral ...
Overview: The Lead Animal Technician will oversee staff in one section or area of the animal facility, perform duties related to the care and feeding of laboratory animals, the processing of dirty and clean caging and maintenance of the Animal Facility. Monday-Friday 7:00 am -3:30pm. Responsibilities: Supervise Technicians in his/her area (facility), specifically: assign tasks, make ongoing as...
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...
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 ...
Fortune-500 Biotech/Pharmaceutical Company is seeking a Compliance Specialist to join their team in Cambridge, MA. The full job description is listed below. Upon receipt of your resume, we will contact you to discuss further details. We look forward to receiving your resume and speaking with you further! OVERVIEW: · Quality Assurance (QA) Bulk Operations is responsible for quality oversight of o...
Position Details: Job Location: Cambridge, MA, 02142 Job Description: TITLE: Sr. Associate II, Safety & Benefit Risk Management (SABR) Operational Excellence and Compliance DEPARTMENT Safety & Benefit Risk Management POSITION SUMMARY Responsible for ensuring departmental compliance with regulatory requirements and department/company operating procedures. Manages the delayed case investigati...
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...
Title: Quality Assurance Specialist II/III The Company: Collegium Pharmaceutical, Inc. is a specialty pharmaceutical company focused on the development of proprietary, late stage pharmaceutical products. These products target market opportunities through formulation based product improvements protected by intellectual property (IP). Collegium is focused on building a portfolio of pain products t...
One of the oldest and most respected pharmaceutical companies in the world has revamped their product initiatives to utilize some of their new technology while maintaining and improving profitability on existing product lines. In their generic pharmaceutical branch they are seeking a highly qualified Sr. Regulatory Specialist. This position will have advanced responsibilities in support of the Reg...
ESIS HSE will be the preferred provider of HSE consulting and compliance services in the unbundled market while maintaining our underwriting and loss control capabilities to support ACE. Our relentless focus on the customer experience will build ourbrand preference. Our customers will describe us as customer-focused,experienced, flexible, creative, and efficient. KEY OBJECTIVE: Provide superior ...
Entry Level - Research Engineer – SolidWorks and LabView LightLine Technologies is a small, high tech company engaged in research, development, and manufacturing. The company’s focus is on advanced optics, electronic hardware, and chemical processing and sensing hardware. (See our website at www.LightLineTech.com). LightLine Technologies is currently engaged in a challenging government-funded re...
Global Clinical Project Leaders (2 open positions) (NJ, CT, MA) Overview: Celldex Therapeutics seeks a Global Clinical Project Leader who will be responsible for overall management of the clinical execution of one of our later stage programs.This position can be based in Hampton, NJ; Needham, MA; or Branford, CT. If the incumbent will be based in NJ or MA, periodic travel to the Branford, CT sit...
Associate Scientist – The Associate Scientist will work within a multi-disciplinary team to conduct research and development of clinical chemistry instrumentation which includes chemical/biological sensors, analytical sequences and reagents. Responsibilities include: maintenance and operation of laboratory equipment for data gathering; blood manipulation and analysis; recording, summarizing and i...
Job Title: Laboratory Technician Location: Framingham, Massachusetts Duties: Join a team dedicated to supporting purification development and other activities within Late Stage Process Development (LSPD), Biologics R&D. Independently performs tasks which include cleaning and sanitizing of lab ware, equipment preparation and sterilization: stocking of all scientific glassware; assistance with o...

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