Biotech Jobs in Acton, Massachusetts

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163 Acton, MA Biotech jobs found on Monster.

Jobs 1 to 20 of 163
EMD 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 to development to production, our scientific expertise and innovative solutions help customers tackle their most compl...
Materials / Chemical Laboratory Technologist Major Responsibilities The Technologist will provide analytical, mechanical, and problem solving support to development, production, and failure analysis efforts in the areas of materials science and chemistry. The work will include consultation on laboratory related technical issues, review of the problem/requirements of work requests, specimen prep...
PHARMACEUITCAL MANUFACTURE PROCESS ENGINEER REQUIREMENT #14-00832 RECRUITER: BRIDGET BURNS JOB LOCATION: DEVENS, MA AUGUST 8, 2014 Project Description: The client in Devens, MA MS&T organization is seeking to fill a Process Engineer position for a 1+ year contract. The successful candidate will provide significant contributions toward technology transfer and process validation activities. 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...
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...
Primary Duties: Under the direction of the Director, Clinical Supply, the Manager, Clinical Supply manages all drug products and devices; packaging, labeling, Shipment and drug return logistical activities by interacting with both internal and external customers and suppliers in order to accomplish project objectives; develops IMP distribution and return drug plans and manages Clinical Supplies Do...
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...
Global Project Manager A Life Science company engaged in medical device design and development. Project teams at this site are interfacing with teams for projects: (a) involving clinical trial validation studies, regulatory submissions, and launch activities as well as (b) projects involving instrument design, development and transfer. An experienced individual with general project management ...
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...
Research Technician Conagen Inc. is a growing Research and Development company located in Bedford, MA. We are currently seeking candidates for a Research Technician position to assist our research scientists in genetic engineering of industrial microbes such as E. coli and yeast. Duties and Responsibilities • Perform basic lab maintenance tasks such as ordering laboratory reagents and small equ...
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...
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...
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...
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...
Job Number: 217164 SAS Programmer REQUIRED KNOWLEDGE, SKILLS AND ABILITIES Knowledge of statistics, programming and/or clinical drug development process In-depth knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines Ability to implement programming specifications, as appropriate Und...
Job Description : Perform analysis and processing of medical imaging data for clinical trials in compliance with study protocols and applicable regulatory agencies. Issue and resolve queries with investigator sites and academic centers to ensure follow-up on imaging-related issues. Validate and maintain a database of medical imaging data and associated results. Key Accountabilities • Perform qu...
Job Description : • Perform quality assurance checks on 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 third party...
•Responsible all activities associated with quarterly commission payouts: maintaining territory alignment, customer files, and targets in TMIC system; calculates commission payments and interfaces with Finance for audit review; communicates achievement to Sales. Works directly with Sales Management to resolve order recognition issues, territory changes, and account assignment. •Works directly wit...
Overview: We are seeking a highly motivated MS/PhD scientist to join the research team of the Translational Oncology Group at the EMD Serono Research & Development Institute, Billerica, MA. The center is located in a suburban setting approximately 12 miles from Cambridge, MA. Company Information: Striving to transform lives through medical science: EMD Serono is the U.S. subsidiary of Merck Se...
The Single-use Sales Development Specialist serves as the primary technical resource for generating opportunities and sales from existing or new customers for a focused technology - this position is specifically responsible for providing highly technical sales support, assuring acceleration(speed) and enhancement (value-add) of the sales cycle to facilitate and drive sales growth within the single...

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