Pharmaceutical Manufacturing Floor Supervisor

SPL Biopharma; Waunakee (WI); Presencial; USD 70.000 - 95.000; Jornada completa

Descripción de la vacante

SPL Biopharma is seeking a Pharmaceutical Manufacturing Floor Supervisor for the 3rd shift (4:00 PM – 4:00 AM, Wed/Thu and alternating weekends) in Waunakee, WI. You will lead a night-shift team, ensure safe, compliant cGMP production, and maintain ALCOA+ documentation in real time.

You will coordinate with operators, manage schedules, and escalate deviations with immediate containment actions. Focus on zero-defect, right-first-time culture and audit readiness.

Formación

• Associate degree required; Bachelor’s degree preferred.
• 3+ years of cGMP manufacturing experience required; at least 1 year in a leadership capacity preferred.
• Demonstrated proficiency with GMP fundamentals, production scheduling, SOPs, and appropriate PPE use.

Responsabilidades

• Lead Operations on the Floor and supervise operators; ensure correct use of process equipment.
• Monitor production in real time, solve routine problems, and act as shift point of contact.
• Maintain alignment to production schedules and build a finite team schedule to meet deadlines.

Conocimientos

Leadership

GMP fundamentals

Production scheduling

SOPs

PPE use

ALCOA+ / documentation

Root cause analysis

Educación

Associate degree

Bachelor’s degree

Descripción del empleo

Pharmaceutical Manufacturing Floor SupervisorYour mission: lead a night-shift team to deliver safe, compliant, and efficient cGMP production—every run, every time. You’ll be the operational anchor on the floor, safeguarding documentation accuracy as work happens and serving as the escalation hub when priorities shift.Shift Details3rd shift coverage: 4:00 PM to 4:00 AM, Wednesdays and Thursdays plus every other weekend.Success Looks LikeManufacturing instructions executed precisely and on schedule; product consistently meets specifications under SOP and cGMP controls.Production resources—people, materials, and equipment—optimized to hit departmental objectives and budget expectations.Real-time issues resolved at the source; clear communication during shift handoffs keeps momentum high.Documentation (batch records, logbooks) accurate and complete at the point of entry, reflecting ALCOA+ principles and a right-first-time culture.Deviations and safety concerns escalated quickly; investigations handled thoroughly with immediate actions and follow-through.Core ResponsibilitiesLead Operations on the FloorProvide hands-on supervision and guidance to operators; demonstrate correct use of process equipment and techniques.Monitor ongoing production, solve routine problems in real time, and act as the shift’s primary point of contact.Maintain alignment to production schedules; build and adjust a finite schedule for your team to meet deadlines.Ensure availability of equipment, supplies, and staffing to avoid bottlenecks.Prepare and compile reports on performance, schedules, goals, equipment issues, and maintenance needs; contribute to analyses and studies as required.Quality, Compliance, and Audit ReadinessReview records as operations progress to ensure completeness and accuracy.Promote best documentation practices (ALCOA+); reinforce a zero-defect, right-first-time mindset.Participate in investigations of deviations, incidents, and OOS results; help drive containment and corrective actions.Maintain continuous compliance with policies, SOPs, cGMP, and safety/housekeeping standards.Support internal/external audits and regulatory inspections; sustain audit readiness.Safety LeadershipEmbed safety into daily routines and decision-making.Enforce correct PPE use and strict gowning practices.Report and escalate safety incidents promptly.People DevelopmentSupervise hourly operators; confirm training and qualification before task assignment.Manage coverage, attendance, and shift rosters; ensure clear expectations and effective on-the-job coaching.Provide feedback, recognize achievements, address performance issues, and conduct performance reviews; strengthen morale through clear objectives and transparent communication of policies.Continuous Improvement & CollaborationTroubleshoot equipment and process challenges; identify root causes and communicate outcomes to senior management.Identify, propose, and help implement process improvements that enhance safety, quality, and throughput.Partner with Quality, Maintenance, Warehouse, and other functions; engage with external vendors and senior leaders as needed.Monitor process data and fulfill reporting requirements through databases, documents, and spreadsheets.QualificationsAssociate degree required; Bachelor’s degree preferred. Relevant experience may substitute for formal education.3+ years of cGMP manufacturing experience required; at least 1 year in a leadership capacity preferred.Demonstrated proficiency with GMP fundamentals, production scheduling, SOPs, and appropriate PPE use.