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- ...QA Validation Specialist Equipment Utilities 6 mth contract Summary : QA Validation role... ...and procedures. Support to production / engineering to ensure the qualified state of... ...validation and computerized system validation (CSV) activities including data integrity compliance...SuggestedFull timeContract work
- ...QA Validation Specialist Lab 6 mth contract Summary : QA Validation role to ensure Qualification... ...overseeing Computer System Validation (CSV) activities including URS FS RA IQ OQ PQ... .... Educational background in Science Engineering or IT with 5 years pharmaceutical or...SuggestedFull timeContract work
- ...Designation/Service provider QA Validation Specialist Reporting to whom... ...and procedures. Support to production / engineering to ensure the qualified state of equipment... ...advice for qualification activities including CSV qualification and data integrity. · Provide...SuggestedFull time
- ...dynamic and fast-paced environment. R&D Partners is seeking a QA Validation Specialist to support the qualification and validation of... ...operations. The successful candidate will work cross-functionally with engineering, production, and quality teams to support ongoing and project-...Suggested
- ...company to play a key role in delivering QA Validation that drives healthcare innovation! R&D... ...with IT, Quality Control, and Engineering teams to ensure robust validation of lab... ...Provide QA oversight during execution of CSV and equipment qualification activities....SuggestedContract work
- ...Are you looking for a new challenge in engineering? Step into a high-impact role where your expertise in utility validation helps power the future of pharmaceutical innovation. R&D Partners is seeking a QA Validation Engineer - Utilities to join a pharmaceutical company...SuggestedContract workTemporary work
£ 38.85 - 60.43 per hour
A global medical device company is seeking a Senior Process Engineer to join their Process Development team. You'll lead the design, optimisation... ...Design-for-test & scalability planning Root cause analysis & validation Support for pre-production/production environments Clear...SuggestedContract workWork at officeImmediate startRemote work- Abbott in Ireland Abbott serves the Irish market with a diverse range of healthcare products, including diagnostics, medical devices, and nutritional products. In Ireland, Abbott employs over 6,000 people across ten sites. We have seven manufacturing facilities located in...SuggestedFull time
£15.54 per hour
Purpose Assist in the development and maintenance of test systems for new product introductions and production. Learn and apply basic engineering principles to support product quality and reliability. Key Responsibilities Support the setup and maintenance of test equipment....SuggestedContract workWork at office- ...enthusiastic Graduate or Junior Automation Engineers with exposure to GMP-regulated... ...Participate in commissioning, qualification, and validation activities (IQ, OQ, PQ) for automated... ...systems or platforms. Knowledge of GAMP5, CSV, data integrity, or validation principles...SuggestedFull timeInternship
- ...possibilities for a brighter tomorrow We are seeking a Process Engineer II on a permanent basis to join our team. Purpose:... ...Demonstrates knowledge and application of Process and equipment validation techniques (IQ, OQ, PQ), FMEA, and associated regulatory requirements...SuggestedPermanent employmentWorldwide
- ...they relate to technology selection system configuration SDLC validation hardware software environments and business processes. Partner... ...Knowledge Skills & Education: Required: BS in Engineering Computer Science or other technical degree. Training completed...SuggestedFull timeContract workLocal areaWorldwide
