Head of Manufacturing

Mantell Associates is partnered with a globally respected Biologics/Biosimilar CDMO, who is seeking an experienced and strategic Head of Manufacturing to lead large‑scale biologics and biosimilar production operations at key US sites in Boston or North Carolina. Reporting to senior leadership, this role is pivotal in delivering high‑quality, GMP‑compliant manufacturing while driving operational excellence and capacity growth. Head of Manufacturing - Responsibilities Provide strategic and operational leadership for biologics and biosimilar manufacturing activities, ensuring adherence to cGMP standards, safety protocols, and regulatory expectations across facilities Oversee daily manufacturing operations, including upstream cell culture/fermentation, downstream purification, formulation, and fill/finish processes Collaborate with cross‑functional partners in Quality, Technical Ops, Engineering, and Supply Chain to ensure seamless production execution and continuous improvement of processes Drive execution excellence for current and pipeline client programs from clinical through commercial supply, meeting timelines, cost, and quality targets Ensure facility readiness and operational resilience through process optimization, capacity planning, risk management, and robust staffing strategies Mentor, develop, and lead high‑performing manufacturing teams, fostering a culture of accountability, continuous improvement, and operational discipline Champion data‑driven decision making and establish clear performance metrics (KPIs) to evaluate operational effectiveness and drive informed actions Represent manufacturing leadership in cross‑site and executive forums, contributing to capacity planning, site investments, and long‑term strategic initiatives Head of Manufacturing - Requirements Bachelor’s or advanced degree in Engineering, Life Sciences, Bioprocessing, or related discipline; advanced degree preferred 10+ years of progressive experience in biologics or biosimilar manufacturing leadership roles, preferably within a CDMO or biopharmaceutical organisation Strong understanding of GMP, quality systems, regulatory compliance (FDA/EMA), and manufacturing best practices for biologics across multiple modalities Demonstrated track record of leading multi‑site manufacturing operations with responsibility for team leadership, throughput delivery, and operational excellence Proven ability to implement continuous improvement methodologies (Lean, Six Sigma, Operational Excellence) in a regulated manufacturing environment Excellent communication, collaboration, and stakeholder engagement skills, with ability to influence teams and senior leaders across functions Strategic leader with hands‑on operational experience and ability to balance high‑level vision with execution rigor Based in or willing to relocate to Boston, MA or North Carolina, USA, with ability to be onsite as required Mantell Associates is a specialist Pharmaceutical and Life Science headhunting firm. For more information on this opportunity, contact us at View phone number on click.appcast.io. #J-18808-Ljbffr