Biotech Jobs in Woburn, Massachusetts

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272 Woburn, MA Biotech jobs found on Monster.

Jobs 1 to 20 of 272
Pine Environmental Services LLC, a leader in the rental industry, is seeking a full time Technician to join our team. The position will be primarily responsible for the maintenance and calibration of our extensive fleet of rental equipment. Our technicians play a vital role within the organization, to ensure our customers receive expertly maintained equipment each and every order. We are looking f...
Pine Environmental Services LLC, a leader in the rental industry, is seeking a full time Driver to join our team. Our drivers play a vital role within the organization to deliver our equipment to our customers in a timely manner. We are looking for a motivated and dedicated person that wants to share in the overall success of our company. Duties & Responsibilities: Ensure timely delivery and pick...
Allied Search Partners is looking for a candidate for a qualifiedBiostatistician.Know someone for this position? We offer a $$ bonus if we place your referral in a position. For a complete list of current Allied Search Partners openings Nationwide please go to: http://www.alliedsearchpartners.com/careers.php Position: Biostatistician Schedule: Full Time Permanent/Direct Hire Location: Winchester,...
About our client: Our client is a global industrial manufacturer responsible for producing protective gear. Job Description: Our client is seeking a Buyer who is an energetic, self-starting, and very capable Professional to be involved collaborating across multiple departments, planning, scheduling and monitoring the movement of materials through the production cycle to determine required material...
As a Research Associate for the Analytical Dept, candidates will be responsible for providing technical expertise in supporting preclinical studies conducted under GLP, ISO 17025, and various other regulatory agencies. Other responsibilities include, but are not limited to:  Performing analysis and troubleshooting utilizing various analytical instruments such as; HPLC, GC, LC/MS/MS, ICPMS, etc. ...
Quality Control Chemist II JOB TITLE: Quality Control Chemist II Our rapidly growing client is looking for a seasoned Quality Control Chemist II that is responsible for performing routine and non-routine analytical chemistry assays of raw materials, in-process samples, finished formulations, special projects, and for performing method development, validation, and transfer activities. This role wil...
Connexion Systems & Engineering, a Boston based IT and Engineering Solutions Company immediately seeks individuals with the following skills: Job# bh2914 Clinical Product Manager Will develop clinical content; to develop market specific solutions; evaluate product utilization and provide recommendations that will improve customer efficiency and adoption. QUALIFICATIONS: BSN or RN required. Case Ma...
Job Description: RU Controller Software Engineer * This position requires candidates to be eligible to for security clearance. US Citizenship Required. * Job Description: Candidate will be required to contribute to the architecture, design and implementation of a system which includes remote device monitoring using digital commands and telemetry. Candidate will need to have experience integrating...
Job Description: Thermal Engineer * This position requires the ability to obtain a Security Clearance In order to apply for a Security Clearance you need to be a U.S. Citizen * Summary: The thermal engineer will be asked to carry out system-level and detailed thermal design, analysis, and testing on optical and communication systems including supporting electronics. Projects range from platform le...
Primary Role: Under the direction of the Senior Director of Regulatory Affairs, direct and manage Regulatory Affairs activities for developing and executing CMC strategies across product life cycles. Manage submissions and interactions with the FDA and other regulatory agencies for CMC issues. Provide regulatory support, guidance and expertise to internal groups such as product development, QA, QC...
Primary Duties: Shire is seeking a highly motivated, multi-talented individual with extensive experience involving all aspects of bioanalytics, and in particular, LC-MS assay development for nucleic acids (mRNA, oligonucleotide, lncRNA, DNA, etc.) with focus on CMC. Candidate is expected to have full proficiency of molecular biology with a strong disposition in analytics (QC, methods, assay develo...
Primary Duties The Lead Medical Writer (MW) is responsible for medical writing activities for a program (eg, a compound with one indication or single indication within a compound or several compounds if scope is small). With some oversight, provides strategic direction to cross-functional project team to ensure that clinical documents (eg, investigators' brochures, study protocol and amendments, s...
Primary Duties: Provides Data Management leadership and expertise to Data Management staff, as well as project and study teams. Act as a member of the Data Management & Clinical Standards Leadership Team (DM&CS LT). Functioning within the Department of Global Clinical Development Operations, the incumbent will be responsible for managing staff and clinical data management operational activities in...
Primary Duties:The Manager CMC Global Regulatory Affairs will direct and manage CMC regulatory strategy of one or more biological and/or small molecule products. This will include formulating and implementing CMC regulatory strategies for the development of protein therapies and CMC regulatory activities for assigned projects in line with US or ICH requirements. Primary role includes: Provide coll...
Primary Role: The Product License Support (PLS) Sr. Specialist is responsible for the planning, publishing (paper, NeES, eCTD), review and delivery of GRO-managed regulatory submissions to global Health Authorities within required timeframes. This role is also responsible for non-submission regulatory reporting on behalf of GRA. The PLS Sr. Specialist represents GRO in special initiatives, process...
PRIMARY ROLES: Responsible for the management of US regional regulatory activities for assigned development and commercially marketed products in the US. The major roles and responsibilities of this position are: i) Responsibility for corporate liaison with FDA and other national regulatory agencies as appropriate; ii) Responsible for the development, content and submission of complete and quality...
. Responsibilities 50% Business Process and Operational Excellence •Oversee the Grants, Charitable Contributions and Sponsorships process and systems to ensure they are executed and operated in compliance with all relevant guidelines and with high quality. •Continuously monitors for process and system efficiency, through operational reporting, direct observation, and client feedback to develop enh...
READING, 01867
As an Army National Guard Chemical Operations Specialist, you'll be there and prepared whenever a community is flooded, an earthquake shakes the foundations of a city, a hurricane makes landfall, or an enemy uses biological or chemical warfare. You will know what to do to evacuate the area, control the situation, and solve the problem. In order to perform these functions, you will be trained to ex...
R&D Senior Scientist (Quantum Magnetics, LLC - Wilmington, MA) Req. Ph.D. in Physics, Chem, or rel. field & 2 yrs’ exp. on the job or 2 yrs’ industry exp. working w/ Ion Mobility Spectrometry &/or Mass Spectrometry. Must have exp. leading a team in conducting trials & certifications for homeland security applications, hands-on exp. in modeling design concepts using SIMION ion optics simulation & C...
CyberCoders Matching Great People with Great Companies Learn more about CyberCoders Apply Senior Director, Biologics Development Lexington, MA Full-Time $140,000 - $200,000 Apply Apply Senior Director, Biologics Development Lexington, MA Full-Time $140,000 - $200,000 Apply Job Details Senior Director, Biologics Development sought to lead a group or scientists and researchers in multiple developmen...

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