We are seeking an experienced
CQV (Commissioning, Qualification, and Validation) Engineer
with over 5 years in the pharmaceutical and cGMP industry. Key Responsibilities:
Lead and participate in Engineering, Procurement, Construction, Validation for GMP facilities. Prepare, execute, and review
IQ, OQ, PQ validation protocols
for equipment, facilities, and utilities. Conduct
root cause analysis
and lead
quality investigations
(deviations, CAPA, change control). Manage
validation schedules
and resource alignment. Support
manufacturing process setup
and technical activities. Perform
FAT/SAT activities
and
temperature mapping . Utilize
Delta V, Kneat, Veeva, and Trackwise . Requirements:
5+ years CQV experience
in pharma/cGMP. Strong understanding of
cGMP, USP, EMA, ICH, 21 CFR, GAMP5, ISPE, PDA, ASME BPE . Proven
problem-solving and project coordination skills . Excellent
communication abilities . Bachelor of Science in
...