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Validation Engineer in Rocky Mount, NC at Synerfac

Date Posted: 3/28/2019

Job Snapshot

Job Description

Will support ongoing projects to determine process capabilities of equipment and utility systems.

Responsibilities will include development of engineering studies, validation protocols, execution of testing, generation of validation reports, and creation change control packages.

Must provide technical support to team members and clients in Quality Assurance, Regulatory, Manufacturing Operations, Deviation Investigations, etc.

Will provide assistance with the Site Change Management Program to keep finished products, equipment, processes and facilities in compliance with contemporary industry standards and regulatory filings.

The position requires knowledge of cGMP and associated industry and regulatory guidance documents.

The candidate must have demonstrated proficiency in project management skills and must be able to balance multiple priorities.

  Job Requirements  


4-year engineering degree.

5+ years of experience in Pharmaceutical Validation/Process Engineering.

Working knowledge of cGMP

MUST have a background in pharmaceutical manufacturing, equipment automation, utilities support systems and clean facilities.

Must have the ability to multi-task and handle multiple competing priorities and requirements.

Must have the ability to work effectively under and manage to strict production, time and performance deadlines.