
Position Description
Senior Process Development Engineer
Location
Remote
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Designs, executes, and optimizes downstream purification unit operations, including Refold, Clarification/Depth Filtration, IEX, HIC chromatography, and TFF/crossflow, to deliver scalable, high-yield, high-purity processes that meet target CQAs.
Process Transfer, Validation, and Technical Support
Provides on-site and remote support for manufacturing processes, addressing technical issues that arise during production.
Reviews and approves GMP documentation, supports investigations by applying rigorous scientific principles and data analysis to solve complex process challenges.
Serves as the DSP representative on CMC teams; integrates with Upstream, Analytical Development, Formulation, Quality, and Regulatory to align development plans, timelines, and deliverables.
Demonstrated expertise in protein chromatography (IEX, HIC), depth filtration, and TFF/crossflow from lab to pilot scale. Conjugation expertise is a plus.
Experience operating ÄKTA systems and control software (e.g., UNICORN), including proficiency in column packing/unpacking and membrane operations.
Familiarity with cGMP expectations for clinical manufacturing and authoring and reviewing cGMP-aligned documentation.
Experience collaborating with manufacturing, supporting engineering and clinical runs, and executing process transfers.
Strong cross-functional communication and stakeholder management in a matrixed environment, with the ability to present complex data clearly to technical and non-technical audiences.
Excellent oral and written communication skills.
8 years of industry experience is required, including 5 years in GMP research, development, operations, manufacturing, pharmaceuticals, or another regulated environment.
Health Insurance (Medical/Dental/Vision)
Disability Insurance
Holiday Pay
Paid Time Off (PTO)
401(k) Match
Employee Stock Purchase Plan
Wellness Programs
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Originally posted by Nektar Therapeutics. View original posting
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