Biotech Jobs in Acton, Massachusetts

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111 Acton, MA Biotech jobs found on Monster.

Jobs 1 to 20 of 111
PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, consulting, and medical communications services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed sig...
QUALITY CONTROL ASSOCIATE FOR RAW MATERIALS REQUIREMENT #14-01228 RECRUITER: JESSICA CLARK JOB LOCATION: DEVENS, MA NOVEMBER 10, 2014 Project Description: To perform routine QC Raw Material chemistry testing in support of Raw Materials and biologics bulk drug substance manufacturing using defined methods in a cGMP compliant laboratory. Assures test results are accurately recorded and abnormal...
MID-LEVEL QUALITY CONTROL ASSOCIATE WITH ANALYTICAL EXPERIENCE REQUIREMENT #14-01224 RECRUITER: MELISSA GIUSTI JOB LOCATION: DEVENS, MA NOVEMBER 7, 2014 Project Description: This position will perform routine testing including Facilities (Water/Gas), STAT testing (In support of Manufacturing), and sample receipt functions. Primary responsibilities include testing of Abatacept using HPLC, UV-V...
SENIOR QA SUPPORT – DRUG SUBSTANCE TECH TRANSFER REQUIREMENT #14-01223 RECRUITER: CINDI PISNOY JOB LOCATION: DEVENS, MA NOVEMBER 7, 2014 Project Description: Provide Quality Assurance oversight to support the commercial technical transfer of drug substance from client’s facility to another facility. This position will be responsible for the following, but not limited to: · QA review and appr...
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 is responsible for the project management of engineering programs. The specifics of the duties can vary depending upon project deliverables as dictated by the R&D disease state project needs; however will include partnership with cross-functional teams, such as Operations, Marketing, Intellectual Property, Sales, Quality Assurance and Regulatory Affairs, in order to meet project deli...
Develops products, materials, capable processes, or equipment for projects of moderate complexity. Under limited supervision/guidance, compiles, analyzes, and reports operational, test, and research data to establish performance standards for newly designed or modified products, processes, and materials. Fully participates in and successfully contributes to project teams typically including the f...
Fortune-500 Pharmaceutical / Biotech Company is seeking two motivated, experienced QC Analysts to join our team. We are seeking one QC Analyst with a focus in QC Microbiology and another with a focus in QC Chemistry. Below are the full details for both opportunities. QC Analyst – Microbiology: · Completes testing of raw materials, in-process and final products in accordance with SOPs for product...
6 Month Contract Position - H1's/Subcontractors will NOT be considered: · 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. · Collect and process samples i...
Client: Growing Biopharmaceutical Company! MUST HAVE: - Bachelor's Degree - 3-5 years experience in the Pharma or Med Device Industry as a CRA Responsibilities: - Assist in designing of study protocols - Organize Data in orderly fashion to allow for accurate & efficient clinical reports - Perform Trial Site visit’s to make sure study & regulatory requirements are being met. - A Resource fo...
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 Summary: The primary responsibility of this position is to develop and lead the implementation of global sourcing and procurement strategies globally to ensure continuity of supply, quality and competitive pricing. Job Responsibilities: Demonstrate skills in global procurement, inventory optimization/planning, and logistics Strong track record of developing and managing Supplier relationsh...
PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, consulting, and medical communications services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed sig...
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. • Perform quality assurance checks...
QUALITY CONTROL LEAD FOR RAW MATERIALS REQUIREMENT #14-01227 RECRUITER: BRIDGET BURNS JOB LOCATION: DEVENS, MA NOVEMBER 10, 2014 Project Description: To provide technical, scientific and project support for the Raw Material Chemistry Quality Control Laboratory in establishing and monitoring testing procedures, investigations, technical transfer of methods, training of staff, and analysis of ...
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 ...
EMD Millipore has an opening for a Lab Manager. This position is located in Billerica, MA. Laboratory Operations Manager: Extractables and Leachables Lab The prime responsibilities in this role would be managing the day to day operations of the Extractables and Leachables Chemistry laboratory, focusing on customer testing supporting EMD Millipore sterile filtration and disposable components. The...
Client: Pharmaceutical Company MUST HAVE: - Bachelor's Degree - 2-5 years of Supply Chain experience from a pharmaceutical or biotech company. Preferred: - Experience with an MRP system. - Authoring of detailed work instructions and/or SOPs - PMBOK and or APICS certification Description: - Candidate will be responsible for overall coordination and management of several Supply Chain projec...

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