R & D Jobs in Woburn, Massachusetts

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230 Woburn, MA R & D jobs found on Monster.

Jobs 1 to 20 of 230
Role Description The candidate will support research programs in the CTI pipeline by leading the CTI Boston Biotherapeutics Technology Group, a group of 8-12 scientists with expertise in phage display, antibody engineering, protein expression and purification. Responsibilities include establishing and executing on aspects of antibody generation and characterization including screening, protein exp...
Job Summary: We are seeking a Marketing Manager responsible for marketing DRG products and services that focus on digital trends shaping the future of consumer and physician marketing. The Marketing Manager will work on messaging, brand development, lead generation activity, marketing collateral, speaking opportunities, webinars, media relations, trade show content and publicity for the companies...
Job Summary: The Software Engineer is responsible for developing new data driven, web-based applications using Ruby on Rails and Ember. This position is based in our Burlington, MA office, but offers flexibility in terms of location and hours (including the ability to work remotely up to 75%). Role Description: Design and develop web functionality using Ruby on Rails, Javascript frameworks such as...
Job Summary: Decision Resources Group (DRG) is seeking a motivated Business Insights Analyst to join our talented and vibrant Infectious Diseases team. With minimal supervision, the Business Insights Analyst will deliver high-quality research and analysis designed for key decision-makers within the biopharmaceutical industry. The ideal candidate will have an entrepreneurial approach to work, exper...
LEXINGTON, 02420
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...
The BA is a bridge between the Business (Need) and the Technology (Solutions). The Business need can be anything about overall business systems (model, process, method etc.) and solutions can be about efficient use of technology (architecture, tool, software application etc.). The BA is required to analyze, transform and ultimately resolve the business problems with the help of technology. The BA...
Primary Duties: The Regulatory Process Standards Lead will further the vision for Global Regulatory Affairs (GRA) in alignment with the One Shire business model to establish and document global process and standards. This position will collaborate with all functions within GRA to design optimum Shire Regulatory processes and interfaces between GRA and Shire functions and contribute to the directio...
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 and manufactu...
Primary Duties: Responsible for the design, development, and validation (both internal and external at CROs) of a broad range of bioanalytical assays including Immunoassays (PK, ADA, and biomarker) and activity or cell-based neutralizing antibody assays to support in accordance with appropriate global regulatory guidance. Schedule activities in accordance with line function and program/corporate g...
Primary Duties: Responsible for assisting the Director, Biostatistics with management and leadership of biostatistics-related activities within therapeutic area through direct product responsibility. Contributes to product development strategy and serves as a statistical expert in registration and communication activities. Represents Shire and provides input to his/her supervisor for statistical i...
PRIMARY ROLES: The Regulatory Technologies and Information Management Lead will further the vision for Global Regulatory Affairs (GRA) in alignment with the One Shire business model to establish and support the new/existing systems and Regulatory information management needs within GRA. This individual will collaborate with all functions within GRA and R&D IT to contribute to the direction and imp...
Primary Duties: The Submissions Portfolio Lead is a team leader with first line accountability for the quality, accuracy and timeliness of regulatory submissions for their assigned business unit(s). This role is responsible for setting the vision for assigned team and collaborating with GRO leadership to set goals, drive process efficiencies and overall operational effectiveness for regulatory sub...
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...
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...
Primary Role: Responsibilities of this position include overseeing the design, development, improvement, qualification, and transfer of immunoassay methods to support studies for process development, product stability and product release. Specific focus will be the development and inventory management of associated critical reagents; this requires outsourcing antibody development/procurement and m...
Primary Role: The Senior Clinical Editor will be required to edit, format, and perform quality control (QC) checks of clinical documents intended for submission to regulatory agencies, as well as assist the Editing and Publishing Team Lead in scheduling and tracking of QC tasks, overseeing external QC vendors as necessary, and identifying, developing, refining, and disseminating QC process improve...
Primary Duties: This position May be based in Wayne, PA or Lexington, MA. Member of the US regulatory affairs team responsible 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, and ii) Responsible for the provision a...
Synageva BioPharma Corp. JOB DESCRIPTION JOB TITLE Associate Director Purification Process Development REPORTING RELATIONSHIP This position reports to the Senior Director of Process Development DATE AVAILABLE Open LOCATION Lexington, MA RESPONSIBILITIES The Associate Director of Purification Process Development is responsible for managing a group whose mission is development of cGMP protein purifi...
Primary Duties: To deliver quality patient engagement and recruitment services that enable study teams to plan, forecast, remodel and deliver on patient enrollment goals, and work to broadly deploy innovative processes, methodologies, data, and technologies for future implementation Responsibilities: 75% Execute and deliver day to day patient engagement and recruitment service and deliverables for...
Primary Role The Global Development Team Leader ("GDTL") will be responsible for the leadership and matrix management of all aspects of 1-4 Development Programs, from the end of preclinical development stage through post-commercialization. The position will be within the Internal Medicine therapeutic area and will focus on transplant medicine. Individuals applying for this role should possess a br...
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