Validation Engineer / Quality Engineer
other jobs Randstad Delivery (GBS)
Added before 4 Days
- England,South East,Oxfordshire
- Full Time, Temporary
- £33,000 - £66,000 per annum
Job Description:
Full job descriptionJob Title: Validation Engineer / Quality Engineer (Contract)Location: Witney, Oxfordshire
Salary: £33,000 - £66,000 per annum (Depending on Experience)
Duration: 12-Month Fixed-Term Contract
About the RoleAre you a sharp, self-starting science graduate looking to make your mark, or an experienced Validation professional seeking a high-impact contract? We are looking for a Validation / Quality Engineer to join our team in Witney.
This is a dynamic, fast-paced role where you will take real ownership of validation activities. From introducing New Product Introductions (NPIs) to supporting a major cleanroom expansion, you will be at the heart of our technical operations.
Whether you are a highly motivated graduate with the right attitude or an industry veteran, we have the scope to tailor this role to your level of experience.
What You’ll Be Doing Day-to-Day*Driving NPIs: Taking the lion’s share of responsibility for introducing New Product Introductions into the business, specifically focusing on equipment qualification.
*Expansion & Validation: Spending roughly two-thirds of your time supporting our exciting cleanroom expansion, managing equipment validation, and executing process validation.
*Continuous Improvement: Managing and executing validation changes on existing machinery.
*Global Collaboration & Approvals: Reviewing and acting as the key approver for change controls across the UK, US, and third-party manufacturers.
*Protocol Ownership: Unlike pure QA roles, you won’t just be reviewing the paperwork-you will actively write and execute the validation protocols.
What We Are Looking ForWe are strictly seeking candidates with a background in the Medical Device or Pharmaceutical sectors.
*Education: A degree in a relevant scientific discipline (e.g., Chemistry, Biomedical Science, or related).
*Experience Levels: * For Graduates: No industry experience? No problem. We want a "no-nonsense," self-starting graduate with exceptional attention to detail and sharp critical thinking skills.
*For Experienced Candidates: Proven experience in Equipment Qualification (IQ/OQ/PQ) and Process Validation within a GMP/regulated medical device or pharma environment.
*Skills: Strong analytical mindset, the ability to work autonomously, and the confidence to handle global stakeholders and third-party manufacturers.
Why Apply?This is a brilliant opportunity to gain or deepen high-level validation experience on a large-scale project (including cleanroom expansions and global supply chain exposure) with a competitive salary package.
To Apply: Please submit your CV highlighting your relevant medical device/pharma experience or your degree credentials.
Randstad Business Support is acting as an Employment Business in relation to this vacancy.
Salary: £33,000 - £66,000 per annum (Depending on Experience)
Duration: 12-Month Fixed-Term Contract
About the RoleAre you a sharp, self-starting science graduate looking to make your mark, or an experienced Validation professional seeking a high-impact contract? We are looking for a Validation / Quality Engineer to join our team in Witney.
This is a dynamic, fast-paced role where you will take real ownership of validation activities. From introducing New Product Introductions (NPIs) to supporting a major cleanroom expansion, you will be at the heart of our technical operations.
Whether you are a highly motivated graduate with the right attitude or an industry veteran, we have the scope to tailor this role to your level of experience.
What You’ll Be Doing Day-to-Day*Driving NPIs: Taking the lion’s share of responsibility for introducing New Product Introductions into the business, specifically focusing on equipment qualification.
*Expansion & Validation: Spending roughly two-thirds of your time supporting our exciting cleanroom expansion, managing equipment validation, and executing process validation.
*Continuous Improvement: Managing and executing validation changes on existing machinery.
*Global Collaboration & Approvals: Reviewing and acting as the key approver for change controls across the UK, US, and third-party manufacturers.
*Protocol Ownership: Unlike pure QA roles, you won’t just be reviewing the paperwork-you will actively write and execute the validation protocols.
What We Are Looking ForWe are strictly seeking candidates with a background in the Medical Device or Pharmaceutical sectors.
*Education: A degree in a relevant scientific discipline (e.g., Chemistry, Biomedical Science, or related).
*Experience Levels: * For Graduates: No industry experience? No problem. We want a "no-nonsense," self-starting graduate with exceptional attention to detail and sharp critical thinking skills.
*For Experienced Candidates: Proven experience in Equipment Qualification (IQ/OQ/PQ) and Process Validation within a GMP/regulated medical device or pharma environment.
*Skills: Strong analytical mindset, the ability to work autonomously, and the confidence to handle global stakeholders and third-party manufacturers.
Why Apply?This is a brilliant opportunity to gain or deepen high-level validation experience on a large-scale project (including cleanroom expansions and global supply chain exposure) with a competitive salary package.
To Apply: Please submit your CV highlighting your relevant medical device/pharma experience or your degree credentials.
Randstad Business Support is acting as an Employment Business in relation to this vacancy.
Job number 3895973
Increase your exposure to recruiters with ProJobs
Thousands of recruiters are looking for you in the Job Master profile database, increase your exposure 4 times with a ProJob subscription
You can cancel your subscription at any time.