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R & D Jobs in Billerica, Massachusetts

871 jobs

Perform quality assurance checks on radiographic and photographic medical imaging data to ensure protocol specific requirements are met Perform established image processing techniques (converting imaging formats, performing preliminary measurements of lesions and volumes) across multiple modalities (including but not limited to CT, MRI, Ultrasound) using proprietary software as well as other thir...
As one of the world’s leading analytical instrumentation companies, Bruker covers a broad spectrum of advanced solutions in all fields of research and development. All our systems and instruments are designed to improve safety of products, accelerate time-to-market and support industries in successfully enhancing quality of life. We’ve been driving innovation in analytical instrumentation for 50 y...
Job Title: Development Engineer Location: Bedford, MA Duration: 12 months+ Job Description: Development Engineer As part of the R&D organization, the successful candidate will design novel products to be used in the processing and purification of biopharmaceuticals. This position will be based at our Bedford, MA campus, with some local travel to internal/external manufacturing sites. The ca...
COMPANY SEEKS SENIOR R&D ENGINEER LeMaitre Vascular is a leading global provider of innovative medical devices for the treatment of peripheral vascular disease. We develop, manufacture and market disposable and implantable vascular devices to address the needs of vascular surgeons and interventionalists. The company is listed on NASDAQ General Purpose of the Job: Works as member of multi-discip...
Fixed Assets Manager Job Location:Wilmington, MA Responsibilities BASIC SUMMARY: Responsible for reviewing/analyzing the transaction activities completed by the accountants as well as overseeing the fixed asset process.Responsible for developing global fixed asset processes and lead continuous improvement activities. ESSENTIAL DUTIES AND RESPONSIBILITIES: • Manage the global fixed asset func...
VALIDATION ENGINEER Our client is seeking a Validation Engineer who will be responsible for manufacturing process and equipment validation and have experience with highly complex capital equipment as well as commissioning, qualification, and validation of equipment and processes. They will also need to understand the quality impact on the product from a validation standpoint. The candidate select...
BASIC SUMMARY: Initiate, direct and execute projects of diverse scope in a GLP environment, working independently (with peer guidance as needed) or as part of a multi-disciplinary team. Develop strategies, applying broad scientific principles and concepts for the preclinical assessment of treatment modalities including pharmaceuticals and medical devices. ESSENTIAL DUTIES AND RESPONSIBILITIES: R...
Development Engineer - Lexington, MA Currently seeking a Development/Bioprocess Engineer with cell culture knowledge/experience. You would be responsible for assisting in the evaluation of the growth, metabolism and product expression of candidate cell lines in bench-scale bioreactors and shake-flasks. Daily Responsibilities: Cell culture sampling, cell counting, metabolite analysis, sample sub...
Laboratory Specialist Lexington, MA 5 Mos Responsibilities Assist in the evaluation of the growth, metabolism and product expression of candidate cell lines in bench-scale bioreactors and shake-flasks. Daily activities include cell culture sampling, cell counting, and metabolite analysis, sample submission for product analyses as well as data management and analysis. The candidate will gain ...
Quality Systems Integration, LLC. Job Description: Validation Engineer The Validation Engineer is part of the Validation group at QSI. The Validation Engineer will review and/or execute primary validation activities for equipment, utilities, computer systems and manufacturing processes at QSI customer locations. Support for all projects will be provided by senior management of QSI. The most crit...
Quality Systems Integration, LLC. Job Description: Quality Engineer The Quality Engineer is part of the Quality group at QSI. The Quality Engineer will review and/or execute primary Quality activities for systems and manufacturing processes at QSI customer locations. Support for all projects will be provided by senior management of QSI. Specific Responsibilitieswill include but are not limited ...
If you are a Senior Manager, CMC & Regulatory Affairs with CMC Biologics experience, please read on! Top Reasons to Work with Us 1. Join an award winning team of scientists! 2. Be part of changing the nature of cancer therapeutics. 3. Experience tremendous personal and professional growth. What You Will Be Doing The Senior Manager, CMC & Regulatory Affairs will be responsible for preparing C...
Review/audit of non-clinical documents to support the preparation for the development of an NDA submission to the FDA and MAA submission to the EMA to support an indication in oncology. Tasks include: Audit of 8 GLP "non clinical" (pre-clinical) study reports Audit of 68 non-GLP non-clinical study reports Reports range in size from 3 pages to 2298 pages (average is 222 pages) Results/findings...
Our client, a global consumer products manufacturer operating in the durable goods, components and consumer electronics space, is looking for an Assistant Manager - R&D to form part of the leadership team in their new office in Cambridge. This position would suit a PhD graduate with the ability to drive the search for new ideas and product innovation in a high-growth environment. Client Details ...
Job Number: 440163 Principal Statistician OVERVIEW: The purpose of this position is to provide compound level / development phase statistical expertise and leadership by: * Independently designing, analyzing and interpreting clinical studies at a compound level for early phase or less complex programs. * Providing strategic statistical input for feasibility assessments, development plans, cro...
Overview: 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: Performs research procedures on mice including but not limited to blood pressure monitoring, body mass composition, hypoxia/hyperoxia experiments, telemetry, behavior...
Regulatory Affairs Manager One of the largest in vitro diagnostic companies in the world is looking for a Regulatory Affairs Manager. The company is a privately owned and works globally to develop, manufacture, and sell measurement technologies. Requirements: Advanced Degree in Sciences 10+ years’ experience in Regulatory Affairs and in medical devices or in vitro diagnostics Knowledge of FDA...
Responsibilities of the Food Scientist: Participate in the testing and development of fluid and cultured Products Procure raw materials and technical information needed for development Prepare and process pilot plant prototypes Participate in production trials and commercialization Record test procedures and observations Coordinate product evaluations Lead shelf life testing of fluid and cu...
Auto req ID 9126BR Title Watson Health - Client Experience Center Manager Job Description Ready to change the way the world works? IBM Watson uses Cognitive Computing to tackle some of humanity’s most challenging problems - like revolutionizing how doctors research cancer or transforming how care is delivered to citizens. This is a crucial role for Watson Health and a phenomenal opportunity for...
PURPOSE OF THE ROLE The Clinical Monitor is an operational role within the New Biological Entity (NBE) group in Quantitative Pharmacology and Drug Disposition (QPD) at EMD Serono to enable operational processes and the delivery of key CRO bioanalytical data to support multiple NBE clinical development programs. As an integral member of a team, the Clinical Monitor will be working closely with the...