Contract Senior Process Engineer

Keros Therapeutics • Lexington, MA

1d • $112 - $124

About The Position

At Keros, our mission is to deliver significant clinical benefit to a wide range of patients with disorders that are linked to dysfunctional signaling of the transforming growth factor-beta (TGF-ß) family of proteins. With a focus on developing differentiated product candidates that are designed to alter TGF-β signaling, we aim to target the pathways critical for the growth, repair and maintenance of blood cells and a number of tissues, including bone, skeletal muscle, adipose and heart tissue. We believe our product candidates have the potential to unlock the full therapeutic benefits of modulating the TGF-β superfamily and provide disease-modifying benefit to patients.

Job Summary:
We are seeking a Contract Senior Process Engineer to join our team. The ideal candidate will have a deep understanding of biologics drug substance production (upstream and downstream), process development, process optimization, scale up, tech transfer, and regulatory submission support. The candidate will work in the Process Development team to transfer processes internally within different types of bioreactors (ie Eppendorf, Sartorius, Applikon) and at different scales (2L up to 200L). The candidate will also engage and work with external partners (CDMOs) to ensure successful process transfer to cGMP manufacturing campaigns and provide technical leadership of deviations, investigations, and change controls. The individual will also serve as a key process owner by evaluating process performance to drive continuous improvements. The individual should also be flexible to provide support for weekend activities for cell culture operations.

Requirements

• BS with 10+ years or MS with 8+ years or PhD with 5+ years of experience in biologics process development (upstream and/or downstream); process scale-up; technology transfer; cGMP manufacturing support; and regulatory submissions for protein therapeutics
• Experience working in process development labs required
• Hands-on experience with aseptic technique, mammalian cell culture maintenance, scale-up principles, and bench-scale bioreactor operations is required.
• Experience with cell culture and/or purification and scale-up
• Experience with different types of bioreactors and control systems
• Understanding of regulatory requirements and experience with authoring and reviewing CMC documents for multiple regulatory submissions
• Excellent collaboration skills and ability to work cross functionally to achieve objectives
• Strong work ethic, motivation, and scientific curiosity

Nice To Haves

• Experience working with CDMOs for facility fit and tech transfer preferred but not required
• Experience with process data analysis and trending and statistical analysis preferred
• Experience with technical support of commercial products in external cGMP manufacturing including investigations and change management

Responsibilities

• Collaborate cross-functionally with process development to deliver manufacturing processes that meet the speed, yield, and product quality requirements of the development programs
• Provide key technical upstream and downstream leadership for development programs including technology transfer, scale up, process design, manufacturing support, and person-in-plant
• Support Process Development team by performing USP or DSP experiments as necessary, with a focus on process scalability across different control strategies
• Perform, develop and optimize robust, efficient, scalable strategies for improving process performance
• Activities will include small-scale studies and pilot scale expression studies
• Analyze complex datasets involving cell growth kinetics, viability, metabolic profiles, and product titers. Identify root causes of process deviations and implement corrective actions.
• Develop scalable upstream processes, establish reliable scale-down models, and author technical transfer documentation to transition protocols seamlessly to pilot and cGMP manufacturing facilities.
• Lead technology transfer activities, including process fit and facility design at external CDMO, ensuring gap analyses and risks assessments are performed technical mitigations are in place for early stage MFG (Phase 1 and Phase 2)
• Author, review and approve technical documentation including protocols, master batch records, and reports related to engineering and GMP runs
• Support continuous process improvement and scale up activities using data analysis for larger scale production while maintaining quality attributes for manufacturing process lifecycle management
• Partner closely with Downstream Process Development, Analytical Development, and Quality Control teams to ensure seamless workflow integration.
• Collaborate cross-functionally to support clinical drug substance manufacturing processes, tech transfer, supply chain, quality compliance, change management and product life cycle management
• Partner with product development, manufacturing, quality and regulatory, lead quality investigations and data analysis as SME to address OOS, OOT, complex deviations/non-conformances and implement change controls to ensure timely/prompt release of batches to meet regional demand forecast and ensure CAPAs are in place
• Cultivate excellent working relationship with CMC stakeholders to deliver successful manufacturing campaigns

Benefits

• This pay range represents the base hourly rate or base annual full-time salary for all positions in the job grade within which this position falls. The actual base salary offer will depend on a variety of factors including experience, education, and other relevant factors.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior