Overview
On Site
Full Time
Skills
Science
Pharmaceutics
Writing
Manufacturing
GMP
Microsoft Excel
Microsoft PowerPoint
Communication
English
Job Details
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.
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