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"Associate Scientist"

Posted on Jun 16, 2020 by eTeam Inc.

Cork, Ireland
Research
Immediate Start
Annual Salary
Contract/Project




P osition Title: Late Development and Stability Sciences -Associate Scientist
Location: Cork
Duration: 12 Months


Our ideal candidate for this role is a candidate with a bit more experience than graduate level, someone with some biotechnology/large molecule in their background, a strong communicator and someone that can hit the ground running and adapt to a busy team environment.

BioTD AD Release & Stability is a department of Pharmaceutical Development and Manufacturing Sciences - Analytical Development (BioTD AD). The department is responsible for Clinical Stability Management and Clinical Release/Stability testing of drug substance and drug product.
The BioTD AD Clinical release & stability department in Cork, Ireland, is responsible for the large molecules scope of the DPDS product portfolio

Position Summary:
Reporting to Senior Scientist, Late Development and Stability Sciences, Clinical Release and Stability Dept., the person represents BioTD AD 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.

Main duties and responsibilities:
Apply analytical knowledge to interpretation of generated data and ensure high quality of the delivered results working with senior colleagues in AD.
Overall release and stability management of product(s) according to portfolio: Evaluate chemical and physical trends. Assist in drawing conclusions on shelf-life, retest period and storage instructions under the guidance of the Scientific Integrator.
Participate in projects as single point of contact building product stability expertise.
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.
Proactively identifies and drives process improvements.
Acts as subject matter expert on assigned analytical techniques..
Presents technical analytical data clearly and concisely to customers, ie, internal and external regulatory inspections.
Keeps abreast of analytical technology and compliance trends.
Execute assigned NME transfer programs and related projects.

Key Skills and Competencies required:
Innovative solutions/technical skills to troubleshoot laboratory issues.
Customer focus and results and performance driven
Sense of Urgency
Ability to work well within team structures and provide leadership.
Solid knowledge of physical, chemical and biological techniques is required.
Excellent communication skills
Good scientific and technical writing skills

Education and Experience:
A minimum of a Bachelor's degree in Biology, Pharmacy or related scientific field is required
At least 3 years experience or related post graduate academic experience is required.
Knowledgeable of FDA/EMEA regulatory requirements applicable to biologics and/or pharmaceuticals.
Practical analytical laboratory experience in a GMP environment is required.







Reference: 900651404

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