MSAT Process Engineer

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 is a leading global consulting group delivering regulatory affairs, pharmacovigilance, quality, and compliance solutions that support pharmaceutical, biotechnology, medical device, and combination product companies across therapeutic modalities, phase-based pathways, and major global markets.

Why explore your future at ELIQUENT?

ELIQUENT Life Sciences is a trusted global consulting firm helping life sciences companies navigate regulatory complexity and bring breakthrough therapies to market. Founded by former regulators and industry experts, we offer end-to-end support in regulatory affairs, pharmacovigilance, and quality compliance. Our team is driven by a shared mission to improve global health through innovation, collaboration, and integrity. At ELIQUENT, you will be part of a purpose-led organization where your expertise contributes to meaningful impact and your growth is supported every step of the way.

About the Role:

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.

Minimum Qualifications:

• Required Industry Experience: Life Sciences / Biopharmaceutical ManufacturingMSAT / Manufacturing Science
• Process Validation
• Upstream Processing
• Filtration Technologies (Filter Press, UF/DF, TFF)
• Process Development & Process Characterization
• DOE and Data Analysis
• GMP Manufacturing Support
• Technical Writing (SOPs, Protocols, Reports)
• Cross-Functional Manufacturing Support

Required Skills:

Protocol and report writing, validation/qualification documentation, engineering project execution, SOP authoring, data analysis, process documentation, cross-functional coordination