Barrington James
Overview
Consultant at Barrington James | Engineering and Manufacturing - USA We are currently partnered with a leading biologics manufacturer seeking experienced Manufacturing Supervisors / Consultants to provide on-site leadership support during an active production scale-up phase. This role will focus on mentoring and developing production supervisors in a regulated environment supporting aseptic formulation, filling, and bulk biologics processing. The ideal consultant will be comfortable working closely on the production floor, coaching supervisors on leadership discipline, deviation management, and compliance behaviors in real time. Responsibilities
Provide hands-on, daily mentorship to production supervisors in upstream, downstream, or fill/finish operations. Reinforce GMP best practices around documentation, deviations, line clearances, and shift handovers. Drive consistency in leadership behavior, communication, and operator engagement across all shifts. Observe active manufacturing and identify opportunities to strengthen process adherence and team accountability. Support supervisors in improving performance metrics such as batch throughput, error reduction, and compliance readiness. Partner with site leadership to deliver feedback and develop sustainable, standardized floor practices. Qualifications
8–10 years of experience in GMP-regulated biologics, pharmaceutical, or sterile manufacturing. Proven background leading or mentoring production teams in a cleanroom or aseptic environment. Strong understanding of cGMP manufacturing processes (formulation, filling, packaging, or bulk biologics). Excellent communication and leadership coaching skills. Flexibility to support multi-shift coverage and travel as required.
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Consultant at Barrington James | Engineering and Manufacturing - USA We are currently partnered with a leading biologics manufacturer seeking experienced Manufacturing Supervisors / Consultants to provide on-site leadership support during an active production scale-up phase. This role will focus on mentoring and developing production supervisors in a regulated environment supporting aseptic formulation, filling, and bulk biologics processing. The ideal consultant will be comfortable working closely on the production floor, coaching supervisors on leadership discipline, deviation management, and compliance behaviors in real time. Responsibilities
Provide hands-on, daily mentorship to production supervisors in upstream, downstream, or fill/finish operations. Reinforce GMP best practices around documentation, deviations, line clearances, and shift handovers. Drive consistency in leadership behavior, communication, and operator engagement across all shifts. Observe active manufacturing and identify opportunities to strengthen process adherence and team accountability. Support supervisors in improving performance metrics such as batch throughput, error reduction, and compliance readiness. Partner with site leadership to deliver feedback and develop sustainable, standardized floor practices. Qualifications
8–10 years of experience in GMP-regulated biologics, pharmaceutical, or sterile manufacturing. Proven background leading or mentoring production teams in a cleanroom or aseptic environment. Strong understanding of cGMP manufacturing processes (formulation, filling, packaging, or bulk biologics). Excellent communication and leadership coaching skills. Flexibility to support multi-shift coverage and travel as required.
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