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- San Diego, CA

Our client - a major Pharmaceutical company in SoCal - is looking for Analytical Chemists. These Chemists will work within the company's Analytical R&D department. Responsibilities will include:Method Development / Method ValidationDevelopment of stability studies Performing literature searches Documenting/Recording all experimental activities in laboratory notebooksThe Qualified Candidate will have analytical methods development experience in a pharmaceutical environment. (4-10+....


Associate Director / Director, Process Development – San Francisco Bay Area Responsibilities: Process Development of small molecule oncology drug candidates from research to validationSubject Matter Expert for process chemistry. Attend CMC meetings, provide status assessments and technical expertiseExperienced organic chemistry skills and leadership abilities to oversee outsourced projects at CRO/CMOCreate technology transfer, scale up and late stage supply chain strategy. Evaluate process....

- Bedminster, NJ

A growing Pharmaceutical company in the Bedminster, NJ area, is looking for an Associate Director QA - CMC. This person will be responsible for ensuring CMC QA document review and approvals are performed in a manner that supports clinical release, regulatory approval, and commercialization of the company’s drug product programs. This person will be responsible for support of the following functional areas: Analytical Manufacturing Microbiology This person will also have responsibility for....


BS Engineering w/5 plus years experience in biotech/pharmaceutical engineering preferredDemonstrated ability to perform hands-on, detailed work, in a fast-paced manufacturing environmentExperience working on the floor in a manufacturing process environment requiredProficient in the design, installation and implementation electro-mechanical control systemsAbility to troubleshoot electrical systems and automated equipment in a GMP environmentKnowledge of practices applied to the preparation of....


The Automation Engineer reports to the Manager of the Automation group. The position is responsible for providing Automation Engineering support. Specific duties include:Working closely with multiple disciplines, including manufacturing, process engineering, process development, utility operations, maintenance, quality assurance, and validation to implement operational improvementsProvide technical support to commercial and clinical manufacturing as needed, specific to process control and....


Top tier Pharmaceutical company (one n Boston and one in NJ nd one in Seattle)Required:Has completed management of a study or group of studies from planning through close out (Phase 3)Experience with managing VendorsExperience working on global studies with CROs Nice to Have:Experience supporting writing clinical study reports,Supporting sNDA or NDA submissions, Supporting pre-Inspection preparation,Participating in Sponsor Inspections by Regulatory BodiesExperience managing or leading teams....

- Boston, MA

My client seeks a Computational Chemist for an applications role. The ideal candidate will support small molecule drug discovery efforts from lead identification to candidate selection. The ideal candidate will take on the following tasks: Liaise with medicinal chemists and project teams to address challenging drug discovery problems with computational chemistry expertise.Leverage proprietary data, design applications, and computional infrastructure in conjunction with commercial tools and....

- San Diego, CA

Computational Chemist My client offers a great opportunity to join a growing, vibrant firm and make an impact on drug discovery and development. The ideal candidate will focus on applying structure and ligand based drug design methods to design molecules with superior pharmacological properties. The ideal candidate will lead and support project teams, and take on the following tasks:Support medicinal chemists and project teams by applying a wide variety of methods to improve potency,....


Director of Quality Assurance My client is focused on cell therapy products, and they actively seek a QA Director. The ideal candidate will take on the following tasks:Establish, develop and manage the quality management system for the firm.Build the quality department infrastructure to assure compliance to company, industry standards and the applicable regulatory requirements.Interface with external personnel (vendors, partners and regulatory bodies) and internal personnel (management and....


Top Tier Global Pharmaceutical company is expanding – Looking for a Director, Clinical Devlopment in their New Jersey office (Jersey City or Madison, NJ) – Supporting their GI programs (Phase III Diabetic Gastroparisis); role will sit in JC for the short term. (Ultimately Madison, NJ). The role will require a MD (GI preferred not required) Must have GI clinical development experience (4-5 years will be sufficient) Will lead and develop Phase III GI program This will be an exciting opportunity....

- Bridgewater, NJ

My client is actively recruiting for a Director of Clinical Operations – this is a high profile position where the Director will be responsible for managing the clinical trial strategy in collaboration with the Medical Affairs Team, regulatory strategy and execution, publications strategy and plan. The ideal candidate will have clinical operations experience in pharma or biotech industries (in the oncology space.) The ideal candidate will take on the following tasks: --oversee clinical trials....

- Philadelphia, PA

My client seeks a Director, Strategic Partnerships and Alliances to form research and clinical collaborations with mostly academic and some biotech partners. The ideal candidate will take on the following tasks: --Identify, prioritize and expand the research and clinical collaborations. --Manage collaborations within the territory and understand the research and drug development needs of current and future partners. --Work as an internal collaborator and leverage multi-faceted opportunities in


My client seeks a Director, Strategic Partnerships and Alliances to form research and clinical collaborations with mostly academic and some biotech partners. The ideal candidate will take on the following tasks: --Identify, prioritize and expand the research and clinical collaborations. --Manage collaborations within the territory and understand the research and drug development needs of current and future partners. --Work as an internal collaborator and leverage multi-faceted opportunities in


My client seeks a Director, Strategic Partnerships and Alliances to form research and clinical collaborations with mostly academic and some biotech partners. The ideal candidate will take on the following tasks: --Identify, prioritize and expand the research and clinical collaborations. --Manage collaborations within the territory and understand the research and drug development needs of current and future partners. --Work as an internal collaborator and leverage multi-faceted opportunities in


My client seeks a Director, Strategic Partnerships and Alliances to form research and clinical collaborations with mostly academic and some biotech partners. The ideal candidate will take on the following tasks: --Identify, prioritize and expand the research and clinical collaborations. --Manage collaborations within the territory and understand the research and drug development needs of current and future partners. --Work as an internal collaborator and leverage multi-faceted opportunities in

- San Francisco, CA

Outstanding opportunity for a Director of Quality for Clinical GCP. My client is seeking a talented Clinical Quality professional who has significant experience in ensuring that Clinical Trials are in compliance with Good Clinical Practice (GCP). Reporting in to the VP, this individual will be responsible for ensuring quality systems, procedures and documentation are in compliance with applicable US and international standards and regulations. While this is initially an individual contributor....


My biotech client seeks a VP, Regenerative Medicine to take on the following tasks: Direct operations including administration, workflow organization, and managing lab personnel and performance (including academic collaborations and CROs.)Guide the method development of FIH combination product.Drive the strategy for translational research development and establish collaborations.Support the development of biologics programs.Serve as an integral member of the discovery and development teams and


Director, Regulatory Affairs / CMC A key leadership position in the therapeutic area of Oncology. Responsibilities include all development activities, marketed products, including CMC, labeling changes, and regulatory compliance of marketed products.Position requires a leader who can generate and effectively implement all strategic initiatives and programs, and communicate the status of all work to leadership and Board of Directors.The position is global in scope and will require the....

- Western, MI

Company:Strong collegial group of people with a very strong team-minded cultureFast-paced work environment on highly technical projectsVery community-minded with a strong sense of giving back to the community with time and talents for charitable organizationsVery strong work-hard, play-hard mentality with fun events outside the officeCompany has grown nationally and this office is slated for growth as wellPrivately-held- you won't be a number hereNationally recognized for innovative,....


Our client - a growing Pharmaceutical company in Raritan, NJ is looking for a Manager - Regulatory Operations. The Manager - Regulatory Operations will be responsible for development and implementation of procedures and systems to support Regulatory Submissions and Regulatory Publishing. The Manager will also be responsible for the establishment and maintenance of an archiving/document management systems and tools (e.g. eDMS, Regulatory Information System, CTD templates, etc.). The Manager....

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