Validation Specialist

3 weeks ago

Dublin, Ireland Cregg Full time

CREGG is currently seeking a CSV Validation Engineer with experience in an automation platform (Rockwell) within a Pharmaceutical environment on a long-term contract.
This is a site-based role, and a Valid Irish work permit is essential.
Responsibilities
Act as the SME within CSV as and when needed
Participate and lead CSV activities linked to Automation projects
Support the preparation of GxP Computerised System Lifecycle documents, including validation plans, requirement specifications, risk assessments, qualification protocols, requirements traceability matrices, and validation reports.
Design, generate and execute test plans and test protocols, managing and reporting findings and non-conformances raised during all types of testing.
Ensure that computer systems and their associated documentation are fully compliant with site specific policies and regulations, good manufacturing practices and industry regulations.
Lead risk assessment before test execution, such such risk assessment includes but not limited to ERES assessment, system functional risk assessment.
Responsible for review of the vendor validation documents, such as validation protocols and validation summary reports.
Participate in deviation investigation, analysis and change assessment.
Support key initiatives and offer concise advise on a range of topics linked within the CSV automation space
Qualifications
Second level qualifications in Electrical, Electronic, Systems Engineering, Computer Science or Equivalent
5+ years' experience working in control systems validation in the Life Sciences/ Pharma sector
Excellent communication and technical writing skills
Experience of PLC/SCADA and OSIsoft PI Data Historian Validation
Knowledge of GAMP software development lifecycle, ANSI/ISA-S88 and S95 industry standards and 21 CFR Part 11
A Valid Irish work permit
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Pharmaceutical Manufacturing
We are not listing role-specific site postings beyond this description.
This is a straight CSV validation engineering role focused on lifecycle documentation, testing, and compliance within a pharmaceutical automation environment.
#J-18808-Ljbffr

  • Cleaning Validation Specialist

    2 days ago

    Dublin, Ireland Quanta part of QCS Staffing Full time

    Cleaning 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...

  • Cleaning Validation Specialist

    3 weeks ago

    Dublin, Ireland Quanta Part Of Qcs Staffing Full time

    Social network you want to login/join with:Cleaning Validation Specialist - Pharmaceuticals - 12 Month Contract - DublinAre 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...

  • Validation Specialist

    2 weeks ago

    Dublin, Ireland Noel Group Full time

    Role: Validation Specialist Reporting to: Engineering and Facilities Manager Location: Dublin 15 Employment Type: Full Time Industry: Logistics and Supply Chain About Us: Noel Group are partnered with a unique supply chain management company with a strong service portfolio within the areas of Transportation, Refrigeration, Storage and Value-Added Services....

  • QC Equipment Validation Specialist

    2 weeks ago

    Dublin, Ireland Life Science Consultants (LSC) Full time

    LSC have a great contract opportunity for a QC Equipment Validation Specialist to join a South Dublin based Biopharmaceutical company that specializes in secondary manufacturing activities such as Formulation, Fill Finish and Packaging. If you have 3+ years of experience working in the pharmaceutical or biotechnology industry and are ready for your next...

  • Validation Specialist

    4 weeks ago

    Dublin, Dublin City, Ireland CREGG Full time

    CREGG is currently seeking a CSV Validation Engineer with experience in an automation platform (Rockwell) within a Pharmaceutical environment on a long-term contract. This is a site-based role, and a Valid Irish work permit is essential.ResponsibilitiesAct as the SME within CSV as and when neededParticipate and lead CSV activities linked to Automation...

  • Senior Qa Validation Specialist

    7 days ago

    Dublin, Ireland Lsc, Life Science Consultants Full time

    OverviewLSC have a great contract opportunity for a Senior Quality Assurance Specialist to join a South Dublin based Biopharmaceutical company that specializes in secondary manufacturing activities such as Formulation, Fill Finish and Packaging.If you have 10 years of experience working in the pharmaceutical or biotechnology industry and are ready for your...

  • Qc Equipment Validation Specialist

    7 days ago

    Dublin, Ireland Lsc, Life Science Consultants Full time

    Role overviewLSC, Life Science Consultants has a contract opportunity for a QC Equipment Validation Specialist to join a South Dublin based biopharmaceutical company that specializes in secondary manufacturing activities such as formulation, fill finish and packaging.Applicants with 3+ years of experience working in the pharmaceutical or biotechnology...

  • QA Validation Engineer

    1 week ago

    Dublin, Ireland Hobson Prior Full time

    Overview Are you looking for a new challenge within the pharmaceutical industry? This role assisting with the launch of two pharmaceutical products is perfect for you. This is an exciting time to join a rapidly growing pharmaceutical company preparing for the commercial launch of two products by the end of the year. With significant investment in...

  • ▷ [15h Left] Senior QA Validation Specialist

    2 weeks ago

    Dublin, Ireland Life Science Consultants (LSC) Full time

    LSC have a great contract opportunity for a Senior Quality Assurance Specialist to join a South Dublin based Biopharmaceutical company that specializes in secondary manufacturing activities such as Formulation, Fill Finish and Packaging. If you have 10 years of experience working in the pharmaceutical or biotechnology industry and are ready for your next...

  • ▷ [Apply Now] Senior QA Validation Specialist

    1 week ago

    Dublin Pike, Ireland LSC, Life Science Consultants Full time

    Overview LSC have a great contract opportunity for a Senior Quality Assurance Specialist to join a South Dublin based Biopharmaceutical company that specializes in secondary manufacturing activities such as Formulation, Fill Finish and Packaging. If you have 10 years of experience working in the pharmaceutical or biotechnology industry and are ready for...