R & D Jobs in Medford, Massachusetts

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708 Medford, MA R & D jobs found on Monster.

Jobs 1 to 20 of 708
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...
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...
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 ...
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...
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...
Position Description: Process Engineer – Filling & Packaging About Civitas Therapeutics Civitas Therapeutics is a privately held company focused on developing transformative therapies through their proprietary pulmonary delivery platform. The technology has the unique ability to deliver large precise doses of drug through a single inhalation, independent of flow rate and utilizing a small breath...
Civitas Therapeutics is a privately held company focused on developing transformative therapies through their proprietary pulmonary delivery platform. The technology has the unique ability to deliver large precise doses of drug through a single inhalation, independent of flow rate and utilizing a small breath actuated device. The lead product is for treatment of Parkinson’s disease, a debilitatin...
Company Confidential Boston, MA, 02109
Currently seeking dynamic sales entrepreneurs for a unique career opportunity in compounding pharmaceutical sales in the greater Boston area. Requirements · 5-7 years pharmaceutical sales experience · Established relationships with specialists in interventional pain management and/or: orthopedics, rheumatology, neurology, endocrinology, podiatry, oncology and primary care physicians. Preferenc...
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 ...
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 ...
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...
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...
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...
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...
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...
Requirements: BA/BS required preferably in Life Sciences; MS is preferred but not required. 3+ years’ experience in medical device industry Minimum of 2 years’ experience handling customer complaints, investigations and/or MDR/Vigilance reporting required Excellent understanding of 21 CFR Part 803 Experience with catheter-based or cardiac assist devices is a huge plus Duties/Responsibilities...
Primary Role The individual will be a senior technical expert to lead or participate in implementation of CAPAs and change controls within the Production Technical Support (PTS) group. Responsibilities will include providing support for upstream and downstream manufacturing operations associated with: -implementation of corrective/preventative actions identified in investigations into process fail...

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