Position: Validation Engineer / Validate Specialist / Quality Specialist / Pharmaceuticals
Salary: £30,000 - £35,000
Location: Cardiff
Validation Engineer / Validate Specialist / Quality Specialist needed to ensure the complete delivery of fully compliant qualification and validation of any equipment, software, facilities, cleaning processes and operational manufacturing processes on site. To ensure the complete delivery of fully compliant Product Quality Review reports and any follow up actions.
This role demands undoubted technical and regulatory knowledge, high standards of attention to detail and the desire to see tasks through to completion.
Validation Engineer / Validate Specialist / Quality Specialist: Key Responsibilities
Preparation, review and approval of validation master plans and validation plans. Preparation, execution, review and approval of qualification and / validation documentation (specifications, protocols, reports etc) in relation to instrument, equipment, utilities etc. Review and approval of third party generated protocols and reports. Review, execution and approval of factory acceptance tests. Review, execution and approval of site acceptance testing (commissioning) activities. Evaluation of equipment / instrument / service suppliers. Management of validation related deviations. Completion of Product Quality Reviews. To comply with internal and external Health & Safety and Environmental Standards as required. To undertake reasonable tasks or projects as and when required within the scope of the job holder’s capabilities and responsibilities. Validation Engineer / Validate Specialist / Quality Specialist: Key Qualifications and Experience:

• Qualified to at least first degree level in Chemistry, Pharmacy or Microbiology or allied sciences.
• Experience in a similar role in the Pharmaceutical Industry with up to date credentials relevant to both investigational (clinical trial) and marketed (commercial products).
• Excellent interpersonal skills being able to communicate effectively with a wide range

of individuals and groups.

• Proven ability and desire to continuously improve.
• Must be able to effectively manage multiple tasks simultaneously.
• Must be a completion driven individual, with the attitude to drive projects to

completion in considerable detail.

• Must be able to initiate and implement change and achieve the buy-in of all staff via

strong influencing skills.
Apply for this role via the X4 Group today.
Or call Lauren Harris on 020 7812 7700 for further details.
Keywords: Validation / Validate / Process / Equipment / GMP / Pharmaceutical / Pharma / Good Manufacturing Practice
TotalJobs.com - 11 months ago