MSAT Process Engineer

ELIQUENT Life Sciences; Los Angeles (CA); On-site; USD 90,000 - 130,000; Full time

Job summary

ELIQUENT Life Sciences is a global consulting firm supporting life sciences companies with regulatory affairs, pharmacovigilance, quality, and compliance solutions across therapeutic modalities and global markets.

In this role you will contribute to filter press development, equipment engineering, production lot documentation, validation protocols, and lifecycle documentation as part of project teams delivering analyses, reports, and SOPs.

Qualifications

• Experience writing protocols and reports in regulated environments.
• Experience with validation/qualification documentation.
• Ability to coordinate cross-functional engineering activities.

Responsibilities

• Prepare and review protocol and report documentation.
• Support life sciences engineering projects and qualification/validation activities.
• Coordinate manufacturing documentation and SOPs.
• Assist in data analysis and technical writing.

Skills

Protocol writing

Report writing

Validation documentation

SOP authoring

Data analysis

Cross-functional coordination

Engineering project execution

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