Life Sciences Manufacturing Consultant – Validation Lifecycle & Requalification
Valspec · Posted Nov 3, 2026
- California, United States
- On-site
- $110K–$120K per year
1–3 jobs· newest first
$110K–$120KOn-site

On-site
$103K–$115K
+10K new in the last hour
Valspec · Posted Nov 3, 2026
Support validation lifecycle activities at a leading biopharmaceutical manufacturing facility in Southern California.
Salary Range: $110,000 - $120,000 annually
Lead a team of validation professionals, maintain validation master plans, review and approve validation protocols and reports, support commissioning, qualification, and validation activities, manage requalification programs, participate in audits and inspections, drive continuous improvement initiatives, serve as validation SME, coordinate with QA, manufacturing, facilities, engineering, and customers, provide technical training and support.
Draft and implement Quality System documentation, author validation protocols, coordinate validation activities, provide input on equipment requirements, support technology transfer, and ensure compliance with regulatory and quality standards.
The salary range for this position ranges from $103,000 - $115,000 per year. In addition, Kashiv BioSciences, LLC., offers a short-term incentive opportunity, such as a bonus or performance-based award with this position within the first 12 months.