Cache of job #13868174

Job Title

Associate Scientist

Employer

FRS Recruitment

Location

Cork

Description

My client is a global pharmaceutical company focused on developing and delivering products to improve people's lives. Due to expansion and ongoing projects they are have a fantastic opportunity for an Associate Scientist to join their team based in Cork. What's in it for you? This is a superb opportunity to work in a Clinical Release & Stability department for a global pharma giant that serve patients with life-improving treatments. Working here will be a fantastic addition to your CV. Your work will truly make a difference to people's lives and you will work alongside cutting-edge technology and a supportive and friendly team. There is a lucrative 10 month contract on offer. About the job: The department is responsible for Clinical Stability Management and Clinical Release/Stability testing of drug substance and drug product. The Clinical release & stability department in Cork, Ireland, is responsible for the large molecules scope of the PDMS product portfolio. Position Summary: Reporting to Associate Director, Late Development and Stability Sciences, Clinical Release and Stability Dept., the person represents CRS in the Global Analytical Forums, will participate and lead on various projects, analytical techniques and testing issues in support of clinical release and stability testing. General Responsibilities: -Overall release and stability management of products according to portfolio. -Takes Lead on critical Lab Continuous Improvement projects and/or serve as representative on cross functional/Process teams. -Write SOP's, protocols, reports and IMPD/IND regulatory filing documents. -Acts as subject matter expert on assigned analytical techniques. -Presents technical analytical data clearly and concisely to customers. -Assist with internal and external regulatory inspections. Execute assigned NME transfer programs and related projects. About you: Bachelor's degree in Biology, Pharmacy or related scientific field. Knowledge of FDA/EMEA regulatory requirements applicable to biologics and/or pharmaceuticals. Practical analytical laboratory experience in a GMP environment is required. Happy to work in a friendly and supportive team. Next Step: APPLY NOW. No updated CV or have some questions before applying? Call Leo for a confidential chat on 086 049 5443 or connect with me on: LinkedIn at http://bit.ly/2tm1My2 or Twitter: This job originally appeared on RecruitIreland.com.

Date Added

2254 days ago

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