MSAT Process Engineer: Validation & Optimization

ELIQUENT Life Sciences; Los Angeles (CA); On-site; USD 120,000 - 170,000; Full time

Job summary

ELIQUENT Life Sciences in Los Angeles, CA is seeking a Process Validation Engineer to design, execute, and document validation protocols ensuring processes meet quality standards and regulatory requirements. You will work with manufacturing, QA, and R&D to identify improvements and troubleshoot issues.

The final deliverables include validation reports and documentation for regulatory submissions and internal audits.

Qualifications

• 3-8 years of experience in life sciences manufacturing and process validation.
• Experience with Upstream Processing, Filtration Technologies, and DOE.
• Strong GMP manufacturing support and technical writing.

Responsibilities

• Design, execute, and document validation protocols to confirm process robustness.
• Collaborate with manufacturing, QA, and R&D to identify improvements.
• Prepare comprehensive validation reports for regulatory submissions and audits.
• Ensure processes are optimized for efficiency, compliance, and product safety.

Skills

Protocol and report writing

Validation/qualification documentation

Engineering project execution

SOP authoring

Data analysis

Process documentation

Cross-functional coordination

Education

MSAT / Manufacturing Science

Job description

ELIQUENT Life Sciences in Los Angeles, CA is seeking a Process Validation Engineer to design, execute, and document validation protocols ensuring processes meet quality standards and regulatory requirements. You will work with manufacturing, QA, and R&D to identify improvements and troubleshoot issues.

The final deliverables include validation reports and documentation for regulatory submissions and internal audits.