Process Validation Engineer, Pennsylvania

Roles & Responsibilities:

Bachelor's degree in science or engineering (MS accepted, PhD is overqualified).

Minimum 2+ years in Process Validation within the biotech/pharma industry.

Writing and executing process validation documents.

Strong Process Performance Qualification (PPQ) experience.

Hands-on experience collecting process samples.

Must have on-the-floor manufacturing experience.

Familiarity with GMP best practices.

Proficient in MS Office (Word, Excel, PowerPoint).

Strong written and verbal communication skills in English.

Ability to work independently and reliably.

Candidates must gown up for the role.

Not a computer validation role – hands-on process validation experience required.

Candidates must provide two professional references (Manager Name, Title, Work Email, and Phone Number) upon submission.