Analytical Technology Specialist II


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https://www.teamhorizon.ie/job-search/473-analytical-technology-specialist-ii/laboratory/scientific/mayo/job2022-03-16 14:49:111970-01-01Team Horizon
Job TypeFixed Term
AreaMayo, IrelandMayoIreland
SectorLaboratory/Scientific
Start Date
AdvertiserMary King
Job Ref2402
Job Views212
Description
 

Team Horizon currently has an exciting opening for Analytical Technology Specialist II to join the diverse Biologics Development Labon our client’s manufacturing facility in Westport, Co. Mayo, on a fixed-term contract basis. Reporting to the Associate Director of Technical Centre, you will be responsible for various activities such as undertaking analysis of in-process, release, stability and investigational analytical activities. You will work with a dynamic, innovative team in supporting and executing Method Transfers, and Validation activities associated with biological drug product analytical processes. You will also be involved in QMS, compiling and reviewing of Laboratory documentation (e.g. SOPs, methods, Master records, Batch Records, Reports) and carrying out routine lab tasks.

 

 

 

What you will be doing:

•    Conduct in process, release, stability & investigational analytical activities

•    Support and execute method transfers and validation activities

•    Compile and review of Laboratory documentation (e.g. SOPs, methods, validation documentation etc.)

•    Train and mentor new members of the team

•    Support regulatory inspections as required

•    Perform routine lab tasks to maintain a high standard of housekeeping

•    Support laboratory projects to ensure timelines are maintained

•    Ensure all testing is carried out in a timely manner to prevent late testing and delays in manufacturing schedule

•    Participate at meetings and provide input to key projects and improvements within the group

 

What you need to apply:

•    You will have a bachelor’s degree in a relevant science discipline with 2-4 years industry experience preferred

•    Experience within a GMP testing laboratory preferred.

•    Working knowledge of QMS (Quality Management System)

•    A clear understanding of working within a GMP, aseptic regulated environment.

•    Excellent communication and presentations skills, both written and oral.

•    Strong analytical skills with the ability to plan and schedule workloads.

•    Drive, high energy, maturity, and ability to work under pressure and deliver results
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