Sr. Supervisor, Manufacturing - Small Scale Purification (Days)
About This Role Our factories run 24/7 operations. Our manufacturing teams work 12-hour shifts (either Days or Nights) on a 2-2-3 calendar rotation.Shift Details: This role follows a 2-2-3 calendar rotation on days (6:00 AM – 6:00 PM ET)Internal Shift Details: Black Day rotating scheduleWe are seeking a Supervisor to lead day shift operations supporting drug substance manufacturing under cGMP conditions. This role oversees Manufacturing Associates, ensures compliant execution of production activities, and drives a culture of safety, quality, and continuous improvement. You will play a key role in coordinating cross-functional activities and delivering manufacturing campaigns in a highly regulated environment.What You'll DoManage, coach, and develop Manufacturing Associates; identify skill gaps and implement development plansSchedule and direct daily manufacturing operations, ensuring alignment with production timelines and prioritiesEnsure all activities are executed in compliance with cGMP standards and that team members are fully trained prior to executionPartner cross-functionally with QC, QA, Materials Management, MS&T, Validation, Facilities, and Engineering to support batch execution, sampling, and validation activitiesLead and support training efforts across safety, GMP, and process-related activities; monitor and improve safety performanceTroubleshoot operational and equipment issues; coordinate maintenance, repairs, and changeovers with FacilitiesDraft and revise manufacturing documentation, including batch records and SOPsWho You AreYou’re a hands-on leader with a strong foundation in drug substance manufacturing and a deep understanding of cGMP operations. You bring both technical credibility and people leadership, with the ability to influence, coach, and drive results in a fast-paced manufacturing environment.Required Skills The following combination of academic and/or relevant experience may be considered:Bachelor’s degree from an accredited college or university, STEM preferred and at minimum 3 years of direct experienceA BioWorks Certificate and/or associate's degree, STEM preferred and at minimum 5 years of direct experienceA High School Diploma (or equivalent) and at minimum 7 years of direct experienceStrong working knowledge of cGMP requirements with the ability to ensure compliant execution of manufacturing activitiesDemonstrated experience being a lead, leading, supervising, coaching, and/or developing manufacturing teamsExperience leading training efforts across safety, GMP, and process-related activities, with a focus on compliance and performancePreferred Skills Experience troubleshooting downstream operational and equipment issues and coordinating maintenance, repairs, and changeoversExperience drafting and revising manufacturing documentation, including batch records and SOPs Job Level: ProfessionalAdditional InformationThe base compensation range for this role is: $98,000.00-$127,000.00Base salary offered i...