EPM Scientific - Phaidon International
Principal Scientist
EPM Scientific - Phaidon International, Los Angeles, California, United States, 90079
Title: Principal ScientistSalary: 150k-170k
Company Summary:
Do you want to change the lives of the people that you work with? Serving patients is our company's number one priority. Achieving greatness, together, is the goal everyday within the world's leading biotechnology company. Manufacturing, researching, and delivering top-shelf products that extend to more than 10 million patients all over the world.
The Principal Scientist will be responsible for:Providing leadership to teams to create commercial manufacturing processes for small and hybrid molecules. Provide expertise and mentorship to junior staffImplementing strategies for development of late phase clinical programs that include both optimization as well as analytical method developmentWorking with product development teams along with leading small molecule programs in clinical process developmentOversee the transfer of methods and aid with cGMP manufacturing at both internal and external manufacturing and testing facilitiesWrite technical reports and analytical CMC sections in regulatory documents and answer to health authorities about product qualityShow expertise in of company's platform and analytical technologies by being innovative and efficient within Process DevelopmentContribute to the development that increase the Attribute Sciences departments efficacyStay up to date on cutting edge literature and technology in the analytical development field in order to provide new methodologies
The Principal Scientist should have the following qualifications:Bachelor's degree and 7 years of Scientific experience ORMaster's degree and 5 years of Scientific experience ORDoctorate degree PhD OR PharmD OR MD and 2 years of Scientific experience
Preferred Qualifications:Exemplary writing skills and attention to detail in writing specifications, technical reports, regulatory filing documents, and methodsBe able to make decisions, multi-task, and solve problems while leading a team and work cross-functionally/globally within CMC teamsNon-GMP and GMP production experience for technical transferKnowledge of early phase development, ICH, FDA, impurities, and genotoxic impuritiesStrong understanding of small molecule analysis (spectroscopic techniques & chromatographic)
Benefits:Retirement & Saving Plan with company contributions, dental and vision coverage, life and disability insurance, flexible spending accounts, and group medicalAnnual bonus program OR (field sales representatives) a sale- based incentive planRemote work arrangementsAward winning time-off plans & bi-annual company-wide shutdownsStock-based long-term incentives
If you are interested in the
Principal Scientist
role, then please don't wait to apply.
#J-18808-Ljbffr
Company Summary:
Do you want to change the lives of the people that you work with? Serving patients is our company's number one priority. Achieving greatness, together, is the goal everyday within the world's leading biotechnology company. Manufacturing, researching, and delivering top-shelf products that extend to more than 10 million patients all over the world.
The Principal Scientist will be responsible for:Providing leadership to teams to create commercial manufacturing processes for small and hybrid molecules. Provide expertise and mentorship to junior staffImplementing strategies for development of late phase clinical programs that include both optimization as well as analytical method developmentWorking with product development teams along with leading small molecule programs in clinical process developmentOversee the transfer of methods and aid with cGMP manufacturing at both internal and external manufacturing and testing facilitiesWrite technical reports and analytical CMC sections in regulatory documents and answer to health authorities about product qualityShow expertise in of company's platform and analytical technologies by being innovative and efficient within Process DevelopmentContribute to the development that increase the Attribute Sciences departments efficacyStay up to date on cutting edge literature and technology in the analytical development field in order to provide new methodologies
The Principal Scientist should have the following qualifications:Bachelor's degree and 7 years of Scientific experience ORMaster's degree and 5 years of Scientific experience ORDoctorate degree PhD OR PharmD OR MD and 2 years of Scientific experience
Preferred Qualifications:Exemplary writing skills and attention to detail in writing specifications, technical reports, regulatory filing documents, and methodsBe able to make decisions, multi-task, and solve problems while leading a team and work cross-functionally/globally within CMC teamsNon-GMP and GMP production experience for technical transferKnowledge of early phase development, ICH, FDA, impurities, and genotoxic impuritiesStrong understanding of small molecule analysis (spectroscopic techniques & chromatographic)
Benefits:Retirement & Saving Plan with company contributions, dental and vision coverage, life and disability insurance, flexible spending accounts, and group medicalAnnual bonus program OR (field sales representatives) a sale- based incentive planRemote work arrangementsAward winning time-off plans & bi-annual company-wide shutdownsStock-based long-term incentives
If you are interested in the
Principal Scientist
role, then please don't wait to apply.
#J-18808-Ljbffr