Aseptic Manufacturing Supervisor - 2nd Shift

At Jabil we strive to make ANYTHING POSSIBLE and EVERYTHING BETTER. We are proud to be a trusted partner for the world's top brands, offering comprehensive engineering, manufacturing, and supply chain solutions. With over 50 years of experience across industries and a vast network of over 100 sites worldwide, Jabil combines global reach with local expertise to deliver both scalable and customized solutions. Our commitment extends beyond business success as we strive to build sustainable processes that minimize environmental impact and foster vibrant and diverse communities around the globe.

Pharmaceutical International, Inc. (Pii), a Jabil company, has an immediate need for an experience Aseptic Production Supervisor to manage 2nd shift aseptic fill manufacturing in Hunt Valley, MD!

• Operational Oversight
  • Oversee daily manufacturing activities during assigned shift
  • Ensure adherence to batch records, SOPs, and aseptic techniques
  • Monitor production schedule and escalate delays or issues
  • Responsible for updating shift manufacturing KPIs
  • Maintains Aseptic Qualification training
  • Strong on-the-floor presence to support team members and ensures quality standards are met and schedules are achieved
  • Enforce safety protocols and PPE compliance
• People Leadership
  • Supervise and support manufacturing operators
  • Conduct shift huddles and provide clear communication on operational priorities
  • Provide coaching and feedback to team members
  • Performs training with staff on the floor as needed
  • Support and demonstrate skill set to Manufacturing Technicians at all levels
• Compliance & Documentation
  • Ensure accurate and timely completion of GMP documentation
  • Maintain inspection readiness and upholds GMP standards within the assigned area
  • Identify and escalate quality concerns or deviations in real time
  • Initiates Deviations in TrackWise.
  • Leads/supports investigations of event and minor classification deviations in TrackWise

• Required Qualifications
  • 3-5 years of experience in GMP-regulated manufacturing environments (e.g., biopharmaceutical, medical device), with at least 3 years in a successful people leadership or supervisory role.
  • Strong understanding of GMP manufacturing processes, cleanroom operations, and aseptic fill-finish.
  • Demonstrated success in leading and developing high-performing teams.
  • Extensive knowledge and application of Good Documentation Practices (GDP).
  • Excellent verbal and written communication skills.
  • Ability to manage multiple priorities and adapt to dynamic operational needs.
• Preferred Qualifications
  • Bachelor's degree in a scientific, engineering, or technical discipline.
  • Experience in deviation management, documentation review, and cross-functional collaboration.
  • Formal training or certification in Lean, Six Sigma (Yellow, Green, or Black Belt), or equivalent continuous improvement methodologies.
  • Experience with sterilization methods (e.g., autoclaving), sterile filtration, and drug product formulation/compounding.

• Ability to travel between and within facilities to visit staff, operations, and projects, as needed.
• Ability to sit, stand, climb stairs, and climb ladders to mezzanines (when necessary).
• Ability to lift up to 40 pounds on occasion.
• Ability to use PPE (safety shoes, goggles, respirators, gloves, etc. when necessary).

• Medical, Dental, Prescription Drug, and Vision Insurance with HRA and HSA options
• 401K Match
• Employee Stock Purchase Plan
• Paid Time Off
• Tuition Reimbursement
• Life, AD&D, and Disability Insurance
• Commuter Benefits
• Employee Assistance Program
• Pet Insurance
• Adoption Assistance
• Annual Merit Increases
• Community Volunteer Opportunities