Overview
On Site
Full Time
Skills
Documentation
Writing
Multitasking
PQ
Science
Startups
HVAC
Pharmaceutics
Manufacturing
URS
Design Review
IDS
IQ
OQ
Problem Solving
Conflict Resolution
Attention To Detail
Microsoft Word
Microsoft Excel
English
Job Details
Responsibilities:
- The Validation Engineer develops documentation for the Commissioning, Qualification, and Validation of pharmaceutical facilities, utilities, and equipment.
- Our Engineers are responsible for protocol writing and execution (field verification), and development of summary reports.
- Ability to multi-task and take initiative to accomplish assigned tasks accurately by established deadlines.
- Ability to work independently.
- Support onsite and offsite activities, such as: FATs, SATs, IOQ and PQ Executions and System Walkdowns.
- BS or MS in a relevant science or engineering field, or equivalent years of hands-on experience.
- 4+ years relevant experience commissioning/validating in an FDA regulated industry.
- Autoclave / Parts Washer Qualification experience is required.
- Experience in 1 or more of the following is desired: facilities and equipment startup, walk downs & troubleshooting, utilities (WFI, RO, HVAC), building automation or other pharmaceutical manufacturing processes and equipment, FAT/SAT, URS, design review, P&IDs, IQ/OQ/PQs, generation & execution, etc.
- Excellent technical problem-solving and troubleshooting skills.
- High attention to detail.
- Expertise in Microsoft Word and Excel
- Excellent oral and written English are required.
- Able to travel domestically and internationally if required.
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.