Senior Process Engineer – Downstream (Biologics & Peptides)
Stark Pharma Solutions Inc
Boulder, CO
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JOB DETAILS
LOCATION
Boulder, CO
POSTED
1 day ago
Job Title: Senior Process Engineer Downstream (Biologics & Peptides)
Location: Boulder, CO (100% Onsite)
Duration: 6 Months + Extensions
Start Date: ASAP
Job Summary
We are seeking a Senior Process Engineer with strong expertise in downstream processing to support the development, scale-up, and commercialization of biologics and peptide-based therapeutics. This role will focus on designing, optimizing, and implementing purification processes and manufacturing systems within a GMP-regulated environment.
The ideal candidate will have hands-on experience with chromatography and tangential flow filtration (TFF) technologies, along with a proven track record supporting process scale-up, equipment qualification, and manufacturing startup activities.
Key Responsibilities
Lead downstream process development and optimization activities for biologics and peptide products
Design, specify, and support implementation of purification systems including chromatography and TFF skids
Support process scale-up from development through pilot and commercial manufacturing
Drive startup, commissioning, qualification, and troubleshooting of downstream manufacturing equipment
Develop and execute process validation and verification strategies aligned with GMP and regulatory requirements
Collaborate with MSAT, Upstream, Manufacturing, and Quality teams to ensure process robustness and consistency
Author and review technical documentation including process descriptions, validation protocols, and regulatory support documents
Serve as a technical SME for downstream purification operations and technologies
Mentor junior engineers and support continuous improvement initiatives
Required Qualifications
Bachelor s, Master s, or PhD in Chemical Engineering, Biochemical Engineering, or related field
8+ years of experience in biopharmaceutical process engineering with strong downstream processing expertise
Hands-on experience with:
Chromatography systems (affinity, ion exchange, HIC, etc.)
Tangential Flow Filtration (TFF) systems
Experience supporting equipment startup, commissioning, and qualification activities
Strong understanding of process validation and GMP manufacturing environments
Experience supporting or leading tech transfer and process scale-up activities
Strong troubleshooting, communication, and cross-functional collaboration skills