What are the responsibilities and job description for the Equipment Validation Engineer position at RevereIT LLC?
Title: Equipment Validation Engineer
Location: Cambridge, MA (Onsite)
We are looking for an Equipment Validation Engineer with 5 years of experience in pharmaceutical manufacturing. In this role, you’ll be responsible for ensuring the qualification and validation of manufacturing equipment, while ensuring compliance with FDA and cGMP standards.
🔹 Key Responsibilities:
- Lead IQ, OQ, PQ protocols for equipment qualification.
- Ensure compliance with FDA 21 CFR Part 211, cGMP, and industry regulations.
- Develop and review validation documentation (protocols, reports, SOPs).
- Collaborate with engineering and quality assurance teams for system optimization.
🔹 Requirements:
- 5 years of experience in equipment validation within the pharmaceutical industry.
- Strong knowledge of cGMP, FDA regulations, and validation protocols.
- Ability to work cross-functionally with engineering and operations teams.
