Field CQV Validation Engineer – Life Sciences

Valspec; Makkah Region; On-site; SAR 337,000 - 412,000; Full time

Benefits offered by this job

Premium medical coverage

401(k) with company match

Tuition reimbursement

Performance incentives

Job summary

Valspec seeks a hands-on Validation Engineer (CQV) to support commissioning, qualification, and validation activities at a pharmaceutical facility in El Segundo, CA. Work directly with equipment, utilities, facilities, and cleanroom systems in a GMP environment.

The ideal candidate has 2–4 years of validation in regulated manufacturing, experience authoring IQ/OQ/PQ docs, and a strong grasp of cGMP. This onsite role offers a challenging project-based environment and ESOP benefits.

Qualifications

• 2–4 years of validation experience in pharmaceutical/biotech or similar regulated environments.
• Equipment Validation (CQV) experience in life sciences manufacturing.
• Direct experience authoring and executing validation protocols.
• Experience generating IQ/OQ/PQ documentation, validation summary reports, and protocol exceptions.
• Strong understanding of cGMP documentation requirements.
• Experience scheduling and executing qualification activities.

Responsibilities

• Execute commissioning, qualification, and validation activities for GMP facilities and manufacturing systems.
• Develop and execute IQ, OQ, and PQ protocols.
• Generate validation protocols, summary reports, deviations, and protocol exceptions.
• Support qualification of facility systems, cleanrooms, HVAC systems, and GMP utilities.
• Schedule, coordinate, and execute qualification activities with cross-functional project teams.
• Review commissioning documentation and ensure readiness for qualification testing.
• Participate in project meetings as the CQV representative.
• Maintain GMP-compliant validation documentation.
• Support startup, troubleshooting, and system turnover activities.
• Work directly in manufacturing and facility environments with significant field presence.

Skills

CQV validation

IQ/OQ/PQ

cGMP documentation

Qualification scheduling

Validation reports

Equipment validation

Job description

Valspec seeks a hands-on Validation Engineer (CQV) to support commissioning, qualification, and validation activities at a pharmaceutical facility in El Segundo, CA. Work directly with equipment, utilities, facilities, and cleanroom systems in a GMP environment.

The ideal candidate has 2–4 years of validation in regulated manufacturing, experience authoring IQ/OQ/PQ docs, and a strong grasp of cGMP. This onsite role offers a challenging project-based environment and ESOP benefits.