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- San Francisco, CA
new job!

DIRECTOR / SENIOR DIRECTOR, REGULATORY AFFAIRS – CMC Our client, a progressive biopharmaceutical company, has a new opportunity for a Senior Director level Regulatory Affairs professional with CMC expertise in the San Francisco Bay area, to drive US and Global Regulatory projects. This is a full-time Senior Director level role with a primary focus on the discovery and development of oncology drugs. Independently manages all regulatory CMC business for oncology products throughout lifecycle.....

- San Francisco, CA
new job!

Our client in the San Francisco Bay area, has a new opportunity for Medical Director with expertise in Oncology NGS. This is a full-time, onsite position, with the opportunity to make an impact, company is seeking a driver to lead change. Medical Director, Oncology NGS San Francisco Bay AreaServes as company’s internal and external oncology / medical expert collaborating with several departments / business units including marketing, market access, salesRespond to questions from physicians and....

- San Francisco, CA
new job!

Vice President, Regulatory Affairs San Francisco Bay Area Our client is seeking a Vice President, Regulatory Affairs who will be responsible for regulatory strategy, oversight, and guidance drug development program. The successful candidate will bring strong leadership abilities to oversee the Regulatory Affairs team, a successful history of effectively leading IND and NDA filings through approval, and interacting effectively with the FDA and other foreign regulatory bodies. This position....

- San Francisco Bay Area, CA
new job!

DIRECTOR, REGULATORY AFFAIRS – CMCSan Francisco Bay Area Our client, a progressive biopharmaceutical company, has a new opportunity for a Senior Director level Regulatory Affairs professional with CMC expertise in the San Francisco Bay area, to drive US and Global Regulatory projects. This is a full-time Senior Director level role with a primary focus on the discovery and development of oncology drugs. Independently manages all regulatory CMC business for oncology products throughout....

- Wyckoff, NJ

My client offers an outstanding culture and exceptional benefits, and they seek a meticulous Technical Writer to oversee a small group and take on the following tasks:Direct the overall process for creating, editing and publishing client reportsOversee variable workload by assigning and coordinating the work of othersEnsure the timely preparation of all manuscripts and responses to reviewer commentsServe as the internal editor-in-chief to establish and maintain a high-quality written....


We are working with a client in the Madison area in need of a Senior Quality Control Analyst. This client is a manufacturer of pharmaceutical ingredients. This position is for an experienced analyst with experience in qPCR and molecular technologies. This opportunity requires this person to be independent and a creative thinker. Responsibilities:Responsible for performing complex and routine laboratory analysis and testing of raw material, finished product and special products.All work is....

- Cambridge, MA

My client seeks an outstanding scientist to contribute to drug discovery and development projects. The ideal candidate will work closely with medicinal chemists and other scientists – and apply methods to improve drug properties and efficacy. In addition, this person will apply and develop cutting-edge techniques and interpret data using modeling and data mining. Finally, the ideal candidate will possess leadership qualities to direct projects and collaborations. The level of the position is....


My client is expanding and looking to hire a Director for their Medical Affairs group. The ideal candidate will take on the following responsibilities:Direct collaborations with academic, pharma and biotech partners and facilitate work with biotech Directors and VPs, academic PIs, and others.Understand the research and drug development needs of existing partners and ensure exceptional service.Develop and expand research and clinical collaborations with new partners. The ideal candidate will....


My client is expanding and looking to hire a Director for their Medical Affairs group. The ideal candidate will take on the following responsibilities:Direct collaborations with academic, pharma and biotech partners and facilitate work with biotech Directors and VPs, academic PIs, and others.Understand the research and drug development needs of existing partners and ensure exceptional service.Develop and expand research and clinical collaborations with new partners. The ideal candidate will....


My client is expanding and looking to hire a Director for their Medical Affairs group. The ideal candidate will take on the following responsibilities:Direct collaborations with academic, pharma and biotech partners and facilitate work with biotech Directors and VPs, academic PIs, and others.Understand the research and drug development needs of existing partners and ensure exceptional service.Develop and expand research and clinical collaborations with new partners. The ideal candidate will....

- Any US State

Our client needs a doctor with experience in oncology clinical drug development to serve as a medical monitor. Work is estimated to take 10 hours per week to start.RequirementsMedical Doctorate (MD) or equivalent5 years clinical drug development experience in oncologyPhase 1 and phase 2 studiesResponsibilities1. Available to clinical investigator sites as a go-to person in the US for checking eligibility2. Be responsible for interacting with sites on safety management of the study. This will....

- Pleasanton, CA

Our large drug/device combo client in Irvine, CA needs a temporary Regulatory Affairs Associate. This contract is estimated to last 12 weeks. This person will coordinate most aspects of company regulatory activities and may interface with domestic and international health authorities. Qualifications: - BS or BA degree, 1-3 years of experience in regulatory affairs. - Experience in a company start-up environment, preferably in medical devices or combination products. - Knowledge of FDA, CA-FDB,

- Seattle OR San Fran, Cali, WA

Top tier Pharmaceutical company in Seattle, WA is expanding They are opening new office as well i nthe San Francisco Bay area of Califronia- this role can be located in either location Full benefits-medical/health, 401k and match, stock, LTis and STis...many progressive benefits...competitive compensation and bonus and more... Full relocation to either area The Sr. Director, Clinical Operations Program Management will be responsible for leading all aspects of clinical operations within the....


Our large pharma client in Irvine, CA is in need of a Sales Analyst on a temp to hire basis. We are one of the few agencies that pays 65% of health insurance costs. MINIMUM REQUIREMENTS: - Bachelor's degree in Business, Computer Science, or Information Technology, Healthcare or related experience preferred. MBA Preferred. - A minimum of 2 years of experience as an Analyst, preferably in a Finance, Sales or Marketing business environment - Advanced Excel Skills are a requirement - Experience....


The Lead Control Systems engineer is responsible for control systems design, specification, programming, simulation and testing, and start-up assistance. Often, this person will be the project technical lead and may be responsible for some project management activities. Design responsibilities include requirements definition, functional and detailed design documentation development. Testing responsibilities include factory and site acceptance test development and execution. Programming....


RETAINED SEARCH ASSIGNMENT Quality Assurance Validation, ManagerVMP – Validation to include: Facility, Utilities, Equipment, Computer, etc.QA Validation MgrMUST have Bio Pharma experienceManage Validation, Write Protocols,Manage EquipmentProject Manager for all Validation ProjectsResponsible that Validations are prepared and executedDesign Validation studies; USA & EUExecute CAPA action plan9CFRDegree BS a Science or relatedPrefer 2+ yrs supervision & experience designing and....


Senior Electrical Engineer We are currently seeking an experienced Electrical Engineer to join our clients technical team. In addition to acting as the lead electrical engineer on projects, you will provide technical guidance to their junior design staff and have the opportunity to work on a range of projects.Position Responsibilities:Lead Electrical Engineer on projects.Responsible for production and review of narratives, drawings, and specifications for all assigned projects.Construction....


Sr Automation Engineer Job Description: As a member of the Engineering and Facilities Reliability Automation team, the successful candidate will be required to support complex and challenging system automation initiatives that require solid understanding of analytical problem solving techniques, project management, lifecycle management and Operational Excellence. This position requires an extensive understanding and background in programming, design, installation and lifecycle management of....


RETAINED SEARCH ASSIGNMENT Quality Assurance Validation, ManagerVMP – Validation to include: Facility, Utilities, Equipment, Computer, etc.QA Validation MgrMUST have Bio Pharma experienceManage Validation, Write Protocols,Manage EquipmentProject Manager for all Validation ProjectsResponsible that Validations are prepared and executedDesign Validation studies; USA & EUExecute CAPA action plan9CFRDegree BS a Science or relatedPrefer 2+ yrs supervision & experience designing and....


Reporting to the Executive Director of Early Development this physician will serve inside the medical sciences group as a leader in Hematology/Oncology early development. This Oncologist will lead early phase clinical development of oncology compounds from first-in-man studies through proof of concept. They will define, design, and execute early phase clinical and translational projects as the initial strategy for drug development. This physician should be trained in Oncology and have....

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