Senior Validation Engineer

Location New Jersey
Discipline: Operations & Manufacturing , Quality Assurance
Job type: Permanent
Salary: £Up to $110k
Contact name: Mark Bux-Ryan

Contact email:
Contact phone: +441293584300
Published: 27 days ago
Duration: Permanent
Expiry date: 31 May 2024 10:59
Startdate: ASAP

​Senior Validation Engineer

Are you a validation expert looking for a new, dynamic environment?

I am partnering with a rapidly growing full service CDMO who are specialised within sterile product development, manufacturing and packaging, and am working with the leadership team to help appoint a number of new hires.

For this specific hire, we are seeking and experience equipment and cleaning / sterilization focused validation expert. With a focus on a range manufacturing and cleanroom equipment (e.g. autoclaves, VHP studies, dry heaters etc.) you will be confident in reviewing existing protocols as well as developing new ones. Managing internal and external / customer relationships is critical as an aspect of the role will be focused on “project” management and ensuring key milestones are met.

For anyone looking to take on the mantle of a subject matter expert, this opportunity is a fantastic one and will genuinely take on a key role, as the company fulfils its growth plans.


  • Bachelors or Masters degree in a related subject

  • At least three years of experience in a pharmaceutical validation activities

  • Understanding of GMP

  • Must have worked within an aseptic environment

  • Strong understanding with a variety of necessary regulations (FDA, ISO, EU and ICH)

CDMO, validation, equipment, cleaning. Sterilization, aseptic, FDA, CQV, commissioning, qualification,