MSAT Process Engineer
Listed on 2026-09-15
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Pharmaceutical
Pharma Engineer, Quality Engineering, Pharmaceutical Manufacturing, Pharmaceutical Science/ Research -
Quality Assurance - QA/QC
Quality Engineering
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
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