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Quality Assurance Validation Specialist

Location: Hull, Yorkshire and the Humber GB

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Job Number: 17573

External Description:

Job Title: Quality Assurance (QA) Validation Specialist 

Location: Yorkshire/Humber   
Contract: Permanent, Full Time 
Work Hours: 37.5 

 

Randstad Sourceright, a leading provider of RPO & MSP Recruitment Services are currently recruiting for a Quality Assurance (QA) Validation Specialist on behalf of a global CDMO organization. 

 

Role Purpose:

In this role you will have the QA oversight and control of site Validation activities to ensure compliance and cover a broad spectrum of validation disciplines, including but not limited to:

  • Process Validation / CPV
  • Facility and Equipment Validation/Qualification
  • Cleaning Validation
  • Storage Area Validation
  • Analytical Method Validation
  • You will ensure validation processes, procedures and execution are in compliance with GMP requirements.

 

Key Accountabilities: 

  • Own the Site Validation Master Plan
  • Implementation and oversight of robust Validation Lifecycle based procedures and business processes with key stakeholders
  • Review and approval of Validation protocols and reports
  • QA lead SME for Validation related topics within Audits and Inspections
  • QA SME for GMP engineering qualification projects, ensuring compliance to site and corporate procedures
  • Design and conduct training and education
  • Oversight of periodic verifications and reports (Equipment, process, temperature mapping etc.)
  • QA Support and input to applicable deviations and change controls
  • Collaborate with key stakeholders to deliver robust business processes and improvements
  • Monitoring and oversight of critical clean utilities from quality perspective (e.g. Purified Water, Nitrogen, Cleanrooms etc.)
  • Work closely with site eCompliance Lead supporting Computer System Validation
  • Ensure data generated/supporting validation is in compliance with ALCOA+ principles throughout its lifecycle



Key Requirements: 

  • Technical experience within GMP / Pharmaceutical environment, including managing projects and validation activities.
  • Broad knowledge of Validation concepts and Lifecycle verification.
  • Focus on high quality; good at planning, organizing and communication.
  • Empowerment, motivating others and development direction.
  • Understands how to effectively engage others within project/change processes.
  • Champion and role model the values of diversity and inclusion through everyday interactions.
  • Ensure clear and direct 2-way communication within their team and other organizations.
  • Able to work cross-functionally, indirectly influencing key stakeholders.
  • Proactive, take responsibility within their area of the business.

Job Number: CONF7809

Community / Marketing Title: Quality Assurance Validation Specialist

Location_formattedLocationLong: Hull, Yorkshire and the Humber GB

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