Validation Specialist
1 day ago
The role: PE Global is currently recruiting for a Validation & Tech Transfer Specialist on behalf of a leading pharmaceutical company based in Dublin. This is an initial 12 month contract role. Description: The Validation & Tech Transfer Specialist will be responsible for developing and maintaining validation (process and cleaning validation, continued process verification) and tech transfer guidance and supporting toolkit to support implementation in a consistent manner across products and sites. This will include ensuring that validation standards and procedures are fit for purpose across multiple modalities and are updated as new modalities are introduced to the pipeline. Responsibilities: Lead, develop and implement scientifically sound, fit for purpose validation and tech transfer guidance based on current regulations, industry standards and industry practices. Drive innovative and efficient approaches to validation and tech transfer incorporating science and risk-based approach. Support the implementation of TT and Validation best practices across the network, work closely with other members of the ATO TT and Validation team on implementation of improvements. Education and Experience: Minimum Bachelors degree in a scientific discipline (Biology, Biochemistry, Biotechnology, Chemistry), or related field. A minimum of 5 years progressive experience the biopharmaceutical or pharmaceutical industry (Product Development, MSAT, Technical Services or Quality). Experience of biopharmaceutical Bulk Drug Substance (BDS) manufacturing and aseptic fill finish. Experience of small molecule API manufacturing and oral solid dose preferred. Extensive knowledge of regulations, current industry practices, and experience of interpretation and application of guidelines and regulations. Strong track record of leading in a global and matrix environment, working cross functionally and developing strong technical talent. Interested candidates should submit an updated CV. Please click the link below to apply, call Kellie on or alternatively send an up to date CV to ***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland*** Although it is not possible for us to respond to all applications, we at PE Global will do our upmost to give you feedback on your application. You have sent your Cv into us as a company and even though you have sent your CV to a particular position, we are making the reasonable assumption that you are active on the job market and as part of our normal recruitment service we will discuss other suitable positions with you. You are free to opt out of this so please specify in your application to us if you just want to be contacted in relation to a specific vacancy. Your Cv is sent to a central recruitment inbox which a number of people in the applicable PE Global division have access to and so this means that you might not be contacted by the named person in this advert. Skills: validation API aseptic drug substance
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Dublin, Ireland Quanta Consultancy Services Ltd Full timeCleaning Validation Specialist - Pharmaceuticals - 12 Month Contract - Dublin Are you looking for the chance to join a life-changing pharmaceutical organisation in their mission to continuously drive innovation? We are recruiting for a Cleaning Validation Specialist for a 12-month contract based in Dublin. Located 15 minutes from Dublin Airport and just a...
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QA System and Validation Specialist
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Cleaning Validation Specialist
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[3 Days Left] Cleaning Validation Specialist
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QA System and Validation
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Dublin, Ireland CPL Full timeThe SK biotek Ireland Quality team at the Swords Campus are looking for a QA Systems & Validation Specialist on a 12 month contract reporting to the Quality Manager. Position Description: The QA Systems Validation Specialist will be responsible for: • Assessment of changes for GMP compliance in accordance with site change control procedure for...
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▷ High Salary! Validation Engineer New
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