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: | mark.bux-ryan@rbwconsulting.com |
Contact phone: | +441293584300 |
Job ref: | MBRUSSVE |
Published: | about 2 months ago |
Duration: | Permanent |
Expiry date: | 29 Jun 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.
Experience:
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,
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