Job Reference: FRS61281
Job Duration:
Start date:
Description:
My client, a biopharma company are seeking an experienced Validation Engineer 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 sitecommissioning plan. Ideally you will have experience in multiple GMP validation disciplines and have strong Technical Writing skills.
* Permanent position
* Highly attractive salary and benefits package on offer
* Fantastic opportunity to join agrowing 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 amultidisciplinary 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 aminimum 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 andstandards 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:
APPLY!
Click Apply now to review the full details and job description for this amazing opportunity or contact Kerry on 0860443981 for an informal chat.
Industry: Pharmaceuticals
Salary: Negotiable, Healthcare, Pension,
Salary Benefits: Negotiable, Healthcare, Pension,
Vacancy Type: Permanent
Job Skills: Validation, GMP, biopharma,
Contact Name: Kerry Rickard
Website: -
Direct Application URL: -