Principal Process Development Scientist

Job Description

Principal Process Development Scientist

Currently partnering with a global CDMO serving pharmaceutical and biotechnology clients. It delivers integrated, end-to-end solutions spanning from early-stage development to commercial supply. Supported by a network of fully-integrated cGMP facilities across Europe and North America, they excel in the development and manufacture of APIs, drug products, and lipid excipients. Its expertise covers diverse technology platforms including Peptides, Oligonucleotides, Lipids & LNPs, Injectables, Highly Potent & Oncology, and Small Molecules.

Very exciting time for them as they look to expand their facility in Boulder, CO. Looking for a Principal Process Scientist, responsible for driving peptide process innovation from the laboratory bench through to commercial-scale production. The individual will design, optimize, and implement robust and cost-efficient manufacturing strategies that support early development, regulatory submissions, technology transfer, validation, and continuous improvement initiatives.

Key Responsibilities

• Lead cross-functional efforts to develop, scale, and optimize peptide manufacturing processes, ensuring delivery against cost, quality, safety, and throughput targets.
• Provide technical leadership in transferring processes from R&D to pilot and commercial facilities, acting as the subject-matter expert during scale-up and plant operations.
• Contribute to long-term strategic planning by delivering detailed project and process data to inform budget forecasts, resource planning, and technology investment decisions.
• Establish and refine experimental procedures and protocols to address complex chemical and technical challenges at both lab and production scale.
• Conduct applied research aimed at improving efficiency, yields, and robustness of peptide synthesis and purification methods.
• Serve as a recognized technical authority within a specific area of peptide chemistry, providing consultation and mentorship to peers and colleagues.
• Ensure full compliance with all internal SOPs, GDP practices, and regulatory requirements in the execution of laboratory and manufacturing activities.

Qualifications & Experience

This position will be on-site in Boulder, CO with relcoation support provided if willing to relcoate.

Apply today or drop me an email - rbanton@barringtonjames.com