Supervisor, Production (3rd Shift)

Job Description:

As a privately-owned, biopharmaceutical company, Ferring pioneers and delivers life-changing therapies that help people build families and live better lives. Our independence helps us cultivate an entrepreneurial spirit and long-term perspective that enables us to achieve growth and scale, while remaining agile and true to our ‘people first’ philosophy. Built on a 70-year plus commitment to science and research, Ferring is relentless in its pursuit of science that drives powerful discoveries and therapies to help people build families, stay healthy, and stand up to the world’s oldest enemy: disease.  

As Supervisor, Production, you will be responsible for overseeing the efficient and compliant operation of the aseptic manufacturing processes. This position requires a combination of technical expertise, leadership skills, and the ability to manage teams to ensure the production of high-quality pharmaceutical products in a controlled aseptic environment.

With Ferring, you will be joining a recognized leader, identified as one of “The World’s Most Innovative Companies” by Fast Company, and honored by Fortune with inclusion on its “Change the World List,” for addressing society’s unmet needs. Ferring US is also Great Places to Work® Certified, distinguishing it as one of the best companies to work for in the country. 

Responsibilities:  

• Lead, mentor, and manage a team of Aseptic Production Operators, ensuring effective execution of aseptic manufacturing processes, adhering to standard operating protocols, and in compliance with regulatory standards.
• Coordinate and supervise daily production activities, including setup, sterilization, formulation, filling, and lyophilization of pharmaceutical products.
• Develop and maintain training programs for Aseptic Production Operators, ensuring their ongoing skill development, safety awareness, and adherence to aseptic techniques.
• Collaborate closely with cross-functional teams, including Quality Assurance, Quality Control, Engineering, and Planning, to ensure seamless production operations and resolve any deviations.
• Optimize production processes by identifying opportunities for efficiency improvements, waste reduction, and operational excellence.
• Lead investigations into deviations, non-conformances, and incidents, implementing corrective and preventive actions to maintain product quality and process integrity.
• Review and approve batch records, process data, and documentation for accuracy, regulatory compliance, and adherence to cGMP (current Good Manufacturing Practices).
• Promote a culture of safety, quality, and continuous improvement among the production team.
• Provide regular performance feedback, conduct performance evaluations, and address employee development needs.
• Comply with policies, guidelines, and regulatory requirements of the Quality System and applicable current Good Manufacturing Practices (cGMPs).
• Manage inventory levels, materials, and equipment to ensure smooth production flow and prevent any disruptions.
• Participate in audits, inspections, and regulatory assessments as required.
• Stay current with industry trends, aseptic technologies, and regulatory updates to ensure compliance and best practices.
• Flexibility to work weekends and holidays dictated by production schedule(s.)

Requirements: 

• Associate’s degree or Bachelor’s degree in relevant Engineering or Scientific discipline may be considered in lieu of industry experience; additional certifications in aseptic techniques, cGMP, or leadership preferred
• 5+ years' experience working in the pharmaceutical/biopharma/biotech industry and within aseptic clean room environments with demonstrated progression in responsibility. Including 3 years   in a supervisory or managerial capacity.
• Profound knowledge of aseptic techniques, cleanroom protocols, cGMP, and regulatory requirements.
• Strong leadership skills with a track record of effectively managing and developing teams.
• Excellent problem-solving and decision-making abilities, with the capacity to handle complex situations and deviations.
• Effective communication skills, with the ability to collaborate across cross-functional teams.
• Flexibility to work in shifts, including evenings, nights, weekends, and holidays, as dictated by production schedules.

Physical Requirements:

• Extended periods of standing, walking, and overseeing pr