R & D Jobs in Woburn, Massachusetts

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768 Woburn, MA R & D jobs found on Monster.

Jobs 1 to 20 of 768
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...
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...
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...
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 ...
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 ...
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...
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...
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 ...
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...
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...
Vice President Regulatory Affairs & Quality Assurance My client is a clinical-stage bio-pharma company focused in neuroscience drug development. They are expanding rapidly over 2014 and anticipate going public in the future. In this brand new role as the Vice President of Regulatory Affairs & Quality Assurance you will lead and promote the organization’s philosophy in quality of development and s...
Job ID: 25198 Date Posted: 07/10/2014 Location: Galleria Job Family: Clinical Research Full/Part Time: Full-Time Regular/Temporary: Regular FLSA Status: Exempt About Dana-Farber Located in Boston, Dana-Farber Cancer Institute brings together world renowned clinicians, innovative researchers and dedicated professionals, allies in the common mission of conquering cancer, HIV/AIDS and related...
Ortho Clinical Diagnostics is recruiting for a Intercompany Accountant , this position will be located in Waltham, MA . Ortho Clinical Diagnostics, Inc. (OCD) is a leading provider ofin vitrodiagnostic products and services, offering accurate, timely, and cost-effective solutions for screening, diagnosing, monitoring and confirming diseases. The company has approximately 3,800 employees around th...

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