Medical Science Liaison US- The MSL will primarily identify and engage with a targeted group of national and regional thought leaders/healthcare professionals as well as payers and managed care accounts, providing the consistent delivery of educational and compliant scientific information in support of our lead product. The MSLs will engage with HCPs, NPs, & PAs who are in clinical practice caring for patients who suffer from psoriasis. They will be trained to respond to complex inquiries in a scientific, fair-balanced, compliant manner serving as a critical field medical resource to these HCPs and company sales and managed markets constituents.
They will be trained to respond to complex inquiries in a scientific, fair-balanced, compliant manner serving as a critical field medical resource to these HCPs and internal sales and managed markets constituents
Director, Regulatory Affairs-MA- The Director of Regulatory Affairs is responsible for developing and managing the regulatory strategy for current and future self-assembling material-based products to ensure the timely preparation of organized and scientifically valid regulatory submissions in various geographic jurisdictions. This individual is also responsible for all regulatory maintenance activities, including periodic reporting requirements for this class III device
Sr. SCIENTIST, ANALYTICAL R&D- CA- My client is a top 20 Global Pharmaceutical corporation. They are looking to hire a Principal Scientist to lead a team of chemists. Must have strong method development and validation experience preferably working with NCE's.
Sr. Research Associate CA- Specialty Pharmaceutical company looking for a Sr Research Associate Analytical R&D. Must be able to independently develop and validate analytical methods specifically working with small molecules. Must also be able to perform methods development and validation for in-process and final product analyses.
QA Manager CA- To ensure all operations are in full compliance with established Standard Test Methods, compendial methods, vendor methods and safety guidelines. Collaborate with QA and Supply Operations to forecast incoming raw materials that require testing. Incumbent must also manage both the raw material and reference standard programs including driving change controls and document change revisions for updates to specification documents as needed.
Sr. PRINCIPAL SCIENTIST, ANALYTICAL R&D- NJ- Top 20 Global Pharmaceutical corporation looking to hire a Sr. Principal Scientist to lead a team of scientists. Must have strong method development and validation experience preferably working with NCE's. Ph.D 8-10 years industry experience or MS 10-12 years of experience.
They will be trained to respond to complex inquiries in a scientific, fair-balanced, compliant manner serving as a critical field medical resource to these HCPs and internal sales and managed markets constituents
Director, Regulatory Affairs-MA- The Director of Regulatory Affairs is responsible for developing and managing the regulatory strategy for current and future self-assembling material-based products to ensure the timely preparation of organized and scientifically valid regulatory submissions in various geographic jurisdictions. This individual is also responsible for all regulatory maintenance activities, including periodic reporting requirements for this class III device
Sr. SCIENTIST, ANALYTICAL R&D- CA- My client is a top 20 Global Pharmaceutical corporation. They are looking to hire a Principal Scientist to lead a team of chemists. Must have strong method development and validation experience preferably working with NCE's.
Sr. Research Associate CA- Specialty Pharmaceutical company looking for a Sr Research Associate Analytical R&D. Must be able to independently develop and validate analytical methods specifically working with small molecules. Must also be able to perform methods development and validation for in-process and final product analyses.
QA Manager CA- To ensure all operations are in full compliance with established Standard Test Methods, compendial methods, vendor methods and safety guidelines. Collaborate with QA and Supply Operations to forecast incoming raw materials that require testing. Incumbent must also manage both the raw material and reference standard programs including driving change controls and document change revisions for updates to specification documents as needed.
Sr. PRINCIPAL SCIENTIST, ANALYTICAL R&D- NJ- Top 20 Global Pharmaceutical corporation looking to hire a Sr. Principal Scientist to lead a team of scientists. Must have strong method development and validation experience preferably working with NCE's. Ph.D 8-10 years industry experience or MS 10-12 years of experience.
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Copyright 2017
Copyright 2017