Sr. PPQ/Tech Transfer Consultant
eliquent life sciencesCarlsbad, CA
Sr. PPQ/Tech Transfer Consultant
L5
eliquent life sciencesCarlsbad, CA2 days ago
Industries
Other Scientific and Technical Consulting ServicesResearch and Development in Biotechnology (except Nanobiotechnology)Biological Product (except Diagnostic) ManufacturingAbout Company
Who Are We?
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:
Support post-PPQ data analysis, data verification, and report preparation. Author or update PPQ protocols, reports, technical assessments, and supporting validation documentation. Provide on-site PPQ execution support and document issues, exceptions, and outcomes. Provide technology transfer support as assigned. Coordinate with MSAT and program stakeholders; detailed reporting structure to be confirmed.
Minimum Qualifications:
Senior-level biologics or biopharmaceutical process validation experience 5-10+ years of experience Familiar with viral vector manufacturing platforms. Hands-on PPQ protocol development, execution support, deviation/exception assessment, data verification, statistical or technical data analysis, and final report authoring. Experience supporting technology transfer and manufacturing readiness in a GMP and / or CDMO environment. Ability to independently develop technical assessments and defensible validation documentation under aggressive timelines. Working knowledge of FDA process validation lifecycle expectations and risk-based decision making. Bachelor’s degree in engineering, life sciences, or a related technical discipline preferred.
Apply now
Level
SeniorL5
Location
Carlsbad, CA
Occupation
Validation Engineers
Industry
Other Scientific and Technical Consulting Services
Posted
2 days ago
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