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- Northern San Jose area, CA
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Sr. Systems Engineering Manager-San Jose area CA Our client, a Fortune 150 Global Supplier of Specialty Medical Diagnostic Equipment manufacturer designing and launching next generation platform and accessories is looking for a Sr Systems Engineering Manager to be hands-on and apply a diversified knowledge of Requirements Definition, Configuration, Risk Management, Human Factors and Usability Engineering principles, practices, and implementation in the development of complex diagnostic....


Director of Business Development My client is expanding and looking to hire a Director of Business Development -- the ideal candidate will develop and grow the flow cytometry biomarker services group. This person will present and promote services to potential clients including new accounts, new business with existing accounts, and new marketing opportunities to establish long term, mutually beneficial business partnerships. The ideal candidate will take on the following....


Director of Business Development My client is expanding and looking to hire a Director of Business Development -- the ideal candidate will develop and grow the flow cytometry biomarker services group. This person will present and promote services to potential clients including new accounts, new business with existing accounts, and new marketing opportunities to establish long term, mutually beneficial business partnerships. The ideal candidate will take on the following....


Director of Business Development My client is expanding and looking to hire a Director of Business Development -- the ideal candidate will develop and grow the flow cytometry biomarker services group. This person will present and promote services to potential clients including new accounts, new business with existing accounts, and new marketing opportunities to establish long term, mutually beneficial business partnerships. The ideal candidate will take on the following....


My client seeks a junior level Scientist to assist in toxicology assessments. The ideal candidate will take on the following tasks:Manage research projects, oversee data quality, ensure regulatory support and liaise with colleaguesDevelop risk assessments for specific toxicology endpoints and provide data interpretationsWrite and edit papers for publication, correspond with journal editors and publishers, and present data at scientific meetings The ideal candidate will possess the following....

- Palo Alto, CA

The Director is primarily accountable for nonclinical toxicology, working in collaboration with nonclinical pharmacology and pharmacokinetic scientists to drive the overall global nonclinical regulatory submission strategy and coordination for multiple company portfolio products, from research to registration and beyond. The individual has experience in evaluating and responding to inquiries from regulatory authorities addressing global nonclinical development issues in support of IND and....


GENERAL DESCRIPTION:This position provides leadership to the manufacturing department engaged in the production of both clinical and commercial drug products. The Associate Director ensures that the production department is adequately staffed with properly trained, knowledgeable employees who perform their duties according to approved Manufacturing directions, Standard Operating Procedures, company guidelines for safety and environmental compliance, as well as current European and US Good....


POSITION SUMMARY: Seeking an engineer to lead projects in support of small molecule clinical and commercial manufacturing processes. The individual will design, develop, scale-up and optimize robust drug product unit operations that provide high product quality at various scales ranging from R&D to cGMP manufacture. Strong collaboration is expected with internal early R&D groups, internal commercial partners, and external third party CMOs. The candidate should have strong communication


Require a highly motivated and experienced individual for the position of Sr. QA Associate II. This individual will be part of the External Commercial QA group. Responsibilities include supporting Supplier Quality Management activities. Performs vendor audits, supports changes, complaints and queries related to external vendors. Troubleshoots issues, develops and implements effective risk mitigation strategies as required. Collaborates with site operations to insure site expectations of....


Director of Business Development My client is expanding and looking to hire a Director of Business Development -- the ideal candidate will develop and grow the flow cytometry biomarker services group. This person will present and promote services to potential clients including new accounts, new business with existing accounts, and new marketing opportunities to establish long term, mutually beneficial business partnerships. The ideal candidate will take on the following....


Global Pharmaceutical Company with Animal Health Division is expanding the Manager of Health & Safety/Environmental/Security is responsible for managing the work activities of exempt and non-exempt staff whose focus and responsibilities include assuring that Clinton Laboratories operates all of its activities in a manner that meets all state, federal and company HSE and security standards. This individual works closely with the other management leaders of the site as well as the corporate....


The Senior Manager Clinical Operations is responsible for developing operational strategy for one or more clinical studies, and leading the cross functional Study Management Team to align and deliver on study goals of data quality, timelines, budget and GCP compliance in support of overall program level plans. Responsibilities: The Senior Manager Clinical Operations Lead will independently plan all aspects of the clinical operations for one or more clinical studies and oversee the execution of


Pharmaceutical company seeking a Quality Control Chemistry Associate I or II for a position based at their Cambridge, MA site initially with a planned move to Norwood, MA in the May/June timeframe. The individual in this role will perform routine testing of raw materials and samples for mRNA products (in process, release and stability) manufactured at the Norwood, MA facility. Also, this individual may support special projects as assigned. He/she will participate in troubleshooting assays and....

- Norwood, MA

Manufacturing Associate (five needs) 1st and 2nd Shifts available 6 month contract, and renewable up to 4 years Company is seeking a cGMP Manufacturing Associate for mRNA Manufacturing of Personalized Cancer Vaccines. This position will eventually transition from Cambridge, MA to our new GMP Manufacturing site in Norwood, MA. The individual in this role will be part of a cohesive team responsible for producing GMP mRNA-based personalized cancer vaccines for evaluation in human clinical trials.


Global Pharmaceutical company is hiring a Director, Scientific Communications- VERY COMPETITIVE base salary, bonus, stock and other Long Term Incentives Succesfull Pharma with marketed products and pipeline of product candidates for chronic diseases that include schizophrenia, depression, addiction and multiple sclerosis. Headquartered in Dublin, Ireland, Company has an R&D center in Waltham, Massachusetts; a research and manufacturing facility in Athlone, Ireland; and a manufacturing....


Global Medical Affairs Director, Immuno-Oncology Our client, a global pharmaceutical company is expanding their I/O portfolio. This is a full-time, onsite, Director level role with the primary focus on immuno-oncology drugs.Company prides itself on a collaborative culture and the opportunity to contribute to purposeful work. Work with Oncology PD-1 products and present data to stakeholders. Lead the medical information review of regulatory documents, publications, labeling, commercial, and....


The Senior Manager, Clinical Development CNS will participate in internal process improvement activities within R&D and Clinical Development. Main Areas of Responsibilities supports the Clinical Program Lead and Clin.Sci. Lead in the development of the Clinical Development Plan and associated clinical trial content (e.g., protocols, IBs/IDFUs, CRFs, CSRs, regulatory submissions and publications) by contributing to scientific/clinical information aligned with the strategy. key Clinical....


My client, a highly regarded New York based research consortium has asked us to search for a Director to lead biologics drug discovery projects in collaboration with academic investigators. You’ll be responsible for lead identification of therapeutic antibodies and proteins, in order to efficiently advance complex research programs from early target validation through animal proof of concept studies. They want a PhD in Immunology, Pharmacology, Molecular or Cell Biology, Biochemistry, or....


My established client seeks a Scientist to take on the following tasks:Perform experiments using behavior assays assessing motor and cognitive dysfunctionDemonstrate strong leadership skills and train/supervise scientists as neededConduct stereotaxic and general surgeriesManage data and perform statistical analysisPrepare and deliver presentations and reports, and contribute to manuscript preparationThe ideal candidate will possess the following qualities:Ph.D. degree in Neuroscience or....


Global Pharmaceutical Company is hiring three Clinical Operations Directors (Vaccine or rare disease or Oncology) This position will be responsible for initiating and leading phase 1 and 2 clinical trials development, set-up, implementation and completion. This will be accomplished by working with the internal project team and through a preferred provider CRO and other external contractors. This role will report internally to the Head of Clinical Operations and work closely with the Regulatory

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