MSAT Process Engineer - Biopharma Manufacturing Validation

ELIQUENT Life Sciences, Inc.; Los Angeles (CA); On-site; USD 120,000 - 180,000; Full time

Job summary

ELIQUENT Life Sciences, Inc. is seeking engineers to support life sciences manufacturing, validation, and documentation activities. The role covers process development, QC coordination, and regulatory-aligned reporting within a GMP environment.

Responsibilities include pilot-scale filter press work, equipment testing, batch record updates, and cross-functional collaboration to ensure lifecycle documentation and validation deliverables meet quality standards.

Qualifications

• Experience in Life Sciences / Biopharmaceutical Manufacturing.
• Experience with process validation and GMP environments.
• Hands-on knowledge of filtration tech and upstream processing.
• Data analysis, DOE methods, and technical writing skills.

Responsibilities

• Filter Press Development: pilot scale runs, comparability studies, protocol/report authoring, execution support, data analysis, QC coordination, analytical testing, SOP development, vendor meetings.
• Equipment Engineering: function testing.
• Production Lot Documentation: batch records, SOPs, forms, specifications, PFMEA updates, CPV workstream support.
• Execute life sciences engineering projects, technical reviews, lifecycle documentation, qualification/validation protocols, final reports, SOPs, and EHS coordination.

Skills

Life Sciences Manufacturing

Process Validation

Upstream Processing

Filtration Technologies

DOE and Data Analysis

GMP Manufacturing Support

Technical Writing

Cross-Functional Coordination

Job description

ELIQUENT Life Sciences, Inc. is seeking engineers to support life sciences manufacturing, validation, and documentation activities. The role covers process development, QC coordination, and regulatory-aligned reporting within a GMP environment.

Responsibilities include pilot-scale filter press work, equipment testing, batch record updates, and cross-functional collaboration to ensure lifecycle documentation and validation deliverables meet quality standards.