Biotech Jobs in Massachusetts

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1000+ Massachusetts Biotech jobs found on Monster.

Jobs 1 to 20 of 1075
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...
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...
Job Title: Quality Control Analyst I Location: Framingham, Massachusetts Duties: Performs operations necessary for quality testing and plays a role in implementing new technology within quality control. At more senior levels, provides an investigative or technological orientation in designing, executing, interpreting and validating quality procedures and test methods. Completes routine testing ...
Job Title: Regulatory CMC Manager Position Description This individual is expected to contribute to the development and implementation of CMC regulatory strategy for products in development with minimal supervision as well as coordinating all aspects of CMC regulatory submissions relevant to their assigned projects or programs. This person will serve as the regulatory CMC representative on rele...
Client: Pharmaceutical Job Title: Brand Protection Senior Specialist Duration: 12+ Months (11/17/2014 to 12/15/2015) Contract on W2 Location: Cambridge, MA, 02142 Brand Protection Senior Specialist Responsibilities: The individual will be responsible for developing Product Protection solutions and associated processes. Product Protection is defined as the application of security features (ov...
Project Scientist – Protein and Serology SeraCare partners with diagnostics researchers, IVD manufacturers and clinical laboratories to shape the future of medical diagnostics. Our innovative portfolio includes ACCURUN® quality controls, research panels, SeraCon® processed biological materials, specialty human blood products and characterized disease state materials. SeraCare helps bridge the gap...
Company Confidential Boston, MA, 02114
Job Description Title: Food Scientist A confidential company north of Boston, MA is seeking a Food Scientist. JOB DESCRIPTION The leader who is hired for this position will support food process technology projects and programs including scale-up and introduction of new products, product quality improvements and productivity increases. Come engage with us as you impact our success as a technica...
Technical Manager Veristat, LLC has an opening for a Technical Manager, Statistical Programming at its Holliston, MA office. The Technical Manager, Statistical Programming independently leads the programming activities for clinical trial projects through mgmt of internal staff. Provide technical support and participate in process and quality improvement initiatives used in the production of ...
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...
GCP QA Consultant This position provides operational support for the quality management system within Global Clinical Operations (GCO.) The AD is responsible for assessing the quality measures, and conducting analysis and reporting to support proactive quality management for GCO related processes. The AD will be a Good Clinical Practice (GCP) expert and will provide quality and regulatory guidanc...
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...
Senior R&D Engineer TEI Biosciences Inc. seeks for a highly driven engineer with a passion for product development and a proven track record of taking products from concept to launch. The successful candidate will have a biomedical/mechanical engineering background with experience developing polymer/biopolymer and tissue-based Medical Device products for human implantation. TEI Biosciences is an...
Summary JOB SUMMARY: Plans, organizes and develops business development activities of the site to contribute to the growth and success of the US business. Conducts regulatory functions aimed at achieving clients' product development and life cycle management goals. Client Details A services company that consults biotechnology, medical technology and pharmaceutical companies in the design and i...
As a member of the Analytical Sciences group in Technical Operations department, the Analytical Scientist I furthers our understanding of the purity, structure and function of a hemophilia bio-therapeutic product to facilitate drug development and manufacturing support. As a technical expert, the Analytical Scientist I develops and optimizes quantitative bio-analytical methods in support of Manufa...
: Pall is a Fortune 1000 materials science and engineering company with the broadest filtration, separation and purification capabilities in the world. Our process and product enabling technologies help our customers make good products better, safer and even possible. We provide innovative products to customers in health care, biotechnology, pharmaceutical, semiconductor, municipal drinking water...
Saint-Gobain, the world leader in the habitat and construction markets, designs, manufactures and distributes building materials, providing innovative solutions to meet growing demand in emerging economies, for energy efficiency and for environmental protection. Saint-Gobain is a welcoming, solid, open-minded company that offers long-term career opportunities. The Northboro R&D Center focusing on...
Seeking a Manufacturing Engineer II for a long-term consulting position at a major medical devices client in Raynham, MA 02767. Qualifications : A minimum of a B.S. in Engineering is required and Mechanical or Manufacturing Engineering is preferred. A minimum of three years’ experience in manufacturing or engineering required. Experience in foundry, precision metal casting, and metal finishing...
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 ...
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...

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