Supervisor, Drug Product Formulation & Inspection (3pm to 11:30pm)

About the role

We are a growing biopharmaceutical manufacturing organization dedicated to producing high-quality drug products that improve lives. Our teams operate in a Good Manufacturing Practices (GMP) regulated environment and collaborate across functions to ensure safety, quality, and reliability at every step.

Responsibilities

• Provide on-the-floor leadership for a shift team of Manufacturing Associates in a current Good Manufacturing Practice (cGMP) environment
• Oversee daily operations for off-shift activities including: Parts Washing, Autoclave operations, Drug Product Formulation, Manual Visual Inspection (MVI), Automated Visual Inspection (AVI)
• Ensure the timely completion of Parts Wash, Autoclave, Formulation, and Visual Inspection activities to support filling operations
• Cook up and execute the manufacturing schedule through daily shift assignments and team huddles
• Serve as the primary point of contact for escalations during the shift; provide clear guidance to resolve issues quickly and safely
• Foster an inclusive, people-first culture through regular communication, one-on-ones on a defined cadence, and team engagement
• Coach, mentor, and develop direct reports; create development plans and support skills growth
• Address employee questions and concerns; identify and close performance gaps, partnering with Human Resources when needed
• Maintain a safe, compliant work environment by ensuring team members have correct and up-to-date training
• Support manufacturing investigations and continuous improvement projects to elevate quality, safety, and efficiency
• Cook up with cross-functional partners for activities requiring access to manufacturing space and equipment (for example: maintenance, calibration, and equipment use)
• Enforce company policies that directly impact employees (for example: time reporting, time-off approvals, shift work, and inclement weather protocols)
• Complete administrative tasks accurately and on time (for example: approving timecards and time off, expense reports)
• Participate in recruitment and retention activities to attract and retain talent, as needed
• Perform other duties, as assigned

Shift and Work Environment

Lead a shift team that supports a 24/7 operating facility
Second shift schedule: 3:00 pm–11:30 pm
Work primarily on the manufacturing floor within a regulated cGMP environment

Knowledge, Skills, and Abilities

• Ability to collaborate effectively with manufacturing and cross-functional teams
• Proficiency with Microsoft Office applications; strong computer literacy
• Clear, effective written and verbal communication
• Willingness to coach, lead, and develop a team
• Strong problem-solving and decision-making skills
• Advanced math and computer skills
• Flexibility to work in support of a 24/7 facility