R & D Jobs in Waltham, Massachusetts

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820 Waltham, MA R & D jobs found on Monster.

Jobs 1 to 20 of 820
Senior Microbiologist Temp to Perm: 6 months contract and then converts Permanent Waltham MA Work in a fast paced environment executing, troubleshooting and developing micro biological test. Responsible for ensuring compliance with regulatory, industry standards and internal laboratory procedures and practices are followed. Key Job Activities: · Create, edit, and review reports for client ana...
New England Research Institutes (NERI) was founded in 1986 and has grown to become a research organization with a global reputation for high-quality research, innovative thinking, and the use of state-of-the-science tools and techniques. NERI continues to be a leader in public health research, clinical trials management, epidemiology, and state of the art media and dissemination research. NERI's ...
QA/QC Specialist III Needed in Lexington, MA Every day, Kelly Services connects professionals with opportunities to advance their careers. We currently have a contract opportunity with a global leader in the biotechnology industry in Lexington, MA. OVERVIEW This position supports the execution of quality systems including the external audit program. This position is responsible for successful, ...
Synageva BioPharma Corp. JOB DESCRIPTION JOB TITLE Manager, Pharmacovigilance REPORTING RELATIONSHIP Senior Director, Pharmacovigilance DATE AVAILABLE Immediately LOCATION Lexington, MA RESPONSIBILITIES Position Overview The Manager, Pharmacovigilance is a seasoned expert in the preparation, analysis, and follow-up of adverse event reports, including preliminary regulatory assessment f...
Manager, Pharmacovigilance Great Pharmacovigilance Opportunity Boston Area We are looking for a seasoned Pharmacovigilance expert who will manage all PV activities for the specified product and or programs in this exciting, high-growth, late stage/early commercial biotech Boston based company. This person will collaborate and act as key product expert with Safety physicians on program activiti...
The purpose of this role is to lead the development and execution of Health Economics and Outcomes Research (HEOR) strategies to evaluate and communicate the economic and humanistic value of Baxalta products within the Immunology franchse to customers and payers. He/she will also provide overall leadership and strategic direction for the HEOR Immunology team on a global scale. This role is based i...
Nuclea Diagnostic Laboratories, a part of Nuclea Biotechnologies, develops a wide range of tests to measure oncogenes, growth factors and growth factor receptors as well as other biomarkers. Our focus is primarily the development and manufacturing of new biomarkers for use as companion Dx. Our in vitro diagnostic assays are used by pharmaceutical, reference laboratories and clinical researchers. N...
Job Title: Clinical Documentation Specialist Position Responsibilities QC Review of pre-study and study documents, coding of administrative and regulatory documents, verification of documentation, and maintenance of document tracking system. Collaborating with CTM to determine and respond to issues in regulatory documentation. Creates study specific document checklists in collaboration with th...
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...
Vericel Corporation (formerly Aastrom Biosciences) is the leader in developing patient-specific expanded cellular therapies for use in the treatment of patients with severe diseases and conditions. The company markets two cell therapy products in the United States, Carticel® (autologous cultured chondrocytes), an autologous chondrocyte implant for the treatment of cartilage defects in the knee, an...
Director, Regulatory Affairs PixarBio seeks a qualified, highly motivated individual to serve as Director, Regulatory Affairs to implement the company’s regulatory strategies for all products. The ideal candidate will provide technical and regulatory expertise to the product teams and in accordance with the current FDA guidelines. The position will report directly to the CEO. Our CEO has been ca...
Product Specialist Needed in Cambridge, MA Every day, Kelly Services connects professionals with opportunities to advance their careers. We currently have a contract opportunity with a global leader in the biotechnology industry in Cambridge, MA. OVERVIEW Supports the management of CMOs responsible for the production of drug substance, drug product and finished goods. Supports tactical operati...
Position Details: Job Title: Product Specialist Job Location:Cambridge, MA, 02142 Duration: 11+ month Job Description : Supports the management of CMOs responsible for the production of drug substance, drug product and finished goods. Supports tactical operations at CMO site(s), including performing inventory transactions, creating batch production documentation, procurement administration, ...
Minimum degree and field of knowledge: PhD or MSc required Years experience required: 5+ Description: We are looking for a Research Specialist to serve as the Manager of the Ragon Institute Virology Core. The Core provides a variety of HIV characterization services such as nucleic acid isolation, viral stock propagation, and viral genome sequencing to researchers both within Ragon, and to the H...
PREFERENCE GIVEN TO LOCAL CANDIDATES Validation Engineer II Summary Ensures that a large number of highly complex pieces of process equipment and systems remain within their validated state and regulatory compliance Responsibilities and Tasks · Executes major engineering challenges pertaining to policies, plans, and objectives · Works with Manufacturing, Facility, and Quality Control design,...
We are seeking an experienced Laboratory Operations Director who will be responsible for controlling production through the Quality Control Laboratory ensuring that all company objectives are met. This candidate should be a self-motivated individual with strong interpersonal skills who is able to motivate, train and monitor other laboratory personnel. Duties: · -Develop and implement strategic b...
Associate Director Regulatory Labeling My client is embarking on global markets as well as emerging markets with an exciting and diverse pipeline. Located in the heart of Boston, they have an executive team offering a well-rounded atmosphere thanks to a nice blend of large and small pharmaceutical experience. They are seeking an Associate Director Regulatory Labeling who will have the opportunity...
QUALITY CONTROL ANALYST We are seeking a highly motivated QC Analyst to join our team responsible for executing QC testing and related analytical activities supporting product development, release and stability. The ideal candidate will have 2-5 years of experience in a cGMP compliant setting; extensive experience with executing QC test methods, generating associated data packages, auditing data ...
The ideal candidate will possess an academic background in physics, chemistry, or electrical engineering, with in-depth experience in physical and chemical principles and practices. In addition, he or she shall possess strong interdisciplinary skills in mechanics, pneumatics, thermodynamics, and materials science. The candidate should also have academic training and industry experience in trace ex...
Description: We're changing the way health care works for the better. That means consulting with our members, partnering with our physicians, and delivering drugs in the most efficient and effective way. Join us and start doing your life's best work.(sm) The epidemiologist has the primary responsibility for the scientific direction and day-to-day management of research projects. It is the epidem...

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