VALIDATION -CQV ENGINEER

United Pharma; California (MO); On-site; USD 90,000 - 120,000; Full time

Job summary

A leading pharmaceutical firm is seeking an experienced Facilities CQV Consultant for a project in California. This hands-on role involves working in an active construction environment, conducting daily site walks, and supporting CQV activities during construction and startup. Ideal candidates will have strong facilities CQV experience, especially with EMPQ and IOV/IQP. The position offers a contract type with a mid-senior level responsibility.

Qualifications

• Strong Facilities CQV experience, especially with EMPQ and IOV/IQP.
• Experience with utilities and process support systems is essential.
• Cleaning Validation experience is a plus.

Responsibilities

• Perform daily construction site walks in full PPE.
• Support CQV activities throughout construction and startup phases.
• Collaborate with Engineering, Construction, and Quality teams.
• Provide hands-on troubleshooting support as required.

Skills

Facilities CQV experience

EMPQ

Vessel IOV & IOPQ

CIP systems

Cleaning Validation

Job description

We are seeking an experienced Facilities CQV Consultant to support a long-term, fully onsite project in Los Angeles, CA. This role requires a hands‑on, field‑based professional who is comfortable working in an active construction and startup environment.

Key Qualifications

• Strong Facilities CQV experience, including:
• EMPQ (Environmental Monitoring Performance Qualification)
• Vessel IOV & IOPQ, including mixing studies and temperature mapping
• Experience with utilities and process support systems, such as:
• CIP systems, CIP skids
• Cleaning Validation experience highly preferred to provide backup support as needed

Day‑to‑Day Responsibilities

• Perform daily construction site walks while working in full PPE
• Support and execute CQV activities throughout construction, commissioning, and startup phases
• Collaborate closely with Engineering, Construction, Quality, and Validation teams to maintain project schedules and deliverables
• Provide hands‑on troubleshooting and field execution support as required

Seniority Level

Mid‑Senior level

Employment Type

Contract

Job Function

Pharmaceutical Manufacturing, Biotechnology Research, and Medical Equipment Manufacturing