Biotech Jobs in Acton, Massachusetts

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93 Acton, MA Biotech jobs found on Monster.

Jobs 1 to 20 of 93
BIOANALYTICAL SCIENTIST WITH HPLC EXPERIENCE REQUIREMENT #14-00666 RECRUITER: KAREN GULUTZ JOB LOCATION: DEVENS, MA OCTOBER 20, 2014 Project Description: Temporary Quality Control Analyst to support Rheumatoid Arthritis Drug while other analyst is dedicated to a Cancer Drug bioassay validation and spec setting GMP •Performs routine testing and data review of in-process, batch release and st...
SENIOR QUALITY CONTROL ASSOCIATE WITH MIRCOBIOLOGY AND CELL CULTURE EXPERIENCE REQUIREMENT #14-01093 RECRUITER: MELISSA GIUSTI JOB LOCATION: DEVENS, MA OCTOBER 6, 2014 Project Description: The Senior Associate, QC Microbiology performs routine Bioburden, Endotoxin, and environmental monitoring testing in accordance with SOPs, safety, and cGMP guidelines to support the release and stability of...
Entegris Job ID 2014-2296 Posted Date 9/8/2014 Job Location US-MA-Billerica Category Engineering & Manufacturing Shift 1st Company Overview and Values: For more than 40 years, Entegris has been a provider of critical products and materials used in advanced high-technology manufacturing. These products and materials are often used to make the building blocks of many of the world's most compl...
Primary Duties: Reporting to the Clinical Documentation Team Lead, the Clinical Document Specialist is responsible for the management of clinical study records (e.g. clinical Trial Master File) from set up through to final archival, ensuring compliance with company SOPs and process. With a focus on inspection readiness, monitors clinical Trial Master File (TMF) compliance and supports preparatio...
Primary Duties: Reporting to the Clinical Documentation Team Lead, the Clinical Document Manager is responsible for overseeing Clinical Documentation Team (CDT) resource management globally, ensuring effective support for Clinical Development Operation's (CDO) document deliverables. Monitors and supports team compliance with regulatory legislation and Shire policy. Oversees effective outsourcing...
ImmunoGen, Inc. of Waltham MA is in search of a Sr. Research Associate to join the Bioanalytical Sciences department. The qualified candidate will be responsible for the development and validation of cell-based and immunochemical assays to support product development stability of antibody drug conjugates from late stage research through clinical testing and licensure. Develop and validate GMP com...
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...
This position will design and develop new products for ANGIODYNAMICS, Inc. from the initial concept stage through demonstration of feasibility. Development of the basic science will involve predictive modeling, prototype design and fabrication, as well as the development and execution of tests (bench and animal) to verify theoretical predictions and evaluate product performance. Refine product de...
Position Summary: Proove Biosciences, Inc. is seeking team players for Research Assistantsto join a fast growing team supporting physician clinics across the nation. Proove Biosciences is the Personalized Pain Medicine Company. Our mission is to Change the Future of Medicine. With offices in Irvine, California and Annapolis-Junction, Maryland, Proove provides physicians with information to improv...
Fermentation Process Development Associate The Process Development Group provides support through the development and optimization of production processes. We work with our R&D and manufacturing colleagues. We are seeking a Research Associate to join our Fermentation Process Development team. This individual will collaborate with Scientists and Process Engineers to design experiments, analyze and...
Senior Scientist – Fermentation Process Development The Process Development Group provides support through the development and optimization of production processes. We work with our Strain Development team and manufacturing colleagues. We are seeking a Fermentation Scientist to join our Process Development team. Responsibilities include all aspects related to development of a robust and scalable ...
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...
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 Description : • Perform quality assurance checks on study images. • Validate and maintain imaging database including images and tracking and review results for assigned projects. • Ensure the site personnel have a good understanding of the protocol, the requirements of the study so that they can fulfill their obligations to complete their study accurately. • Perform established image proce...
EMD Millipore has an opening on the North America Field Marketing team. We are seeking a Technical Consultant with a strong experience in solid dose formulation of drugs. This is a field based position and not limited to MA. Headquarters is located on Middlesex Turnpike in Billerica, MA. The candidate is expected to have the following key skills: Residential expert on oral solid dose formulation ...
COMPANY Randstad in partnership with EMD Serono is seeking a qualified Research Informatics Scientist to join the Research Informatics team in Billerica, MA. PURPOSE OF THE ROLE The purpose of this role is to develop and implement new solutions for research informatics systems, as well as to provide end user supports. KEY TASKS & RESPONSIBILITIES - Develop new informatics applications to supp...
Primary Duties This position has two primary responsibilities: 1. Global Health Economics , Outcomes Research and Epidemiology (GHEORE) Product (s) support Responsibilities as a member of a Global product team representing and helping execute the GHEORE product strategy. In this capacity you will support the GHEORE product team(s) to which you will be assigned to coordinate and articulate the i...
Primary Role Under the direction of the Director of Regulatory Affairs direct and manage Regulatory Affairs activities for developing global CMC strategies across product life cycles & execution in North America. Provide collaborative support for execution of global strategies to other regions (EU & International). Manage submissions and interactions with the FDA and Health Canada for CMC issues....
Primary Role: • Drives clinical activities of one or more Programs including life cycle management (LCM) and co-leads the development operations team (DOT) • In collaboration with the DOT, defines clinical strategy (clinical development plan, CDP) which is aligned with the Program strategy as defined by the global development team (GDT) • Responsible for the benefit/risk clinical assessment, in...
Primary Duties: • Drives clinical activities of one or more Programs including life cycle management (LCM) and co-leads the development operations team (DOT) • In collaboration with the DOT, defines clinical strategy (clinical development plan, CDP) which is aligned with the Program strategy as defined by the global development team (GDT) • Responsible for the benefit/risk clinical assessment, ...

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