Validation Engineer

Job Overview

My client, a pharmaceutical company are seeking a experienced Validation Engineers to join their team.

Reporting to the Head of Engineering, you will be part of a dedicated team assisting in the implementation and operation of the site commissioning plan. Ideally you will have experience in multiple GMP validation disciplines and have strong Technical Writing skills.

  • Permanent AND contract positions available
  • Highly attractive salary and benefits package on offer
  • Fantastic opportunity to join a growing and innovative organisation at an exciting stage of the business.
  • Friendly, inclusive and collaborative working environment. Teamwork and new ideas are very much encouraged
  • Excellent opportunities for career progression and advancement.
  • Days only role - with flexible working hours.

Responsibilities ( A snapshot…)

  • Effectively working within a multidisciplinary team to Prepare, schedule and execute Commissioning, Qualification and Validation protocols
  • Lead Risk assessments for process and equipment as required.
  • Develop system impact assessments, validation plans, protocols and reports that support the qualification and validation of systems.
  • Execute Commissioning and validation of manufacturing equipment, downstream equipment and processes in addition to supervising and witnessing Validation / Qualification carried out by vendors.

Requirements

  • You will hold a BSc/MSc or BEng/MEng in Engineering or related discipline.
  • Ideally you will have a minimum of 5+ years' experience in validation, quality systems, operations, engineering or any combination thereof.
  • Experience in multiple GMP validation disciplines (process equipment, utility, automation, computer systems, sterilization) with advanced technical knowledge.
  • Validation experience using risk based approach guidelines, international regulatory requirements and standards and other in.
  • Experience interacting with or creating material for representatives of regulatory agencies and executive level staff.
  • Experience with investigations into manufacturing deviations and determination of product impact potential, root cause and corrective actions.

Next Steps:

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