GMP Operations Supervisor | 12h Night Shift, On-Site

Catalent Pharma Solutions; Saint Petersburg (FL); On-site; USD 75,000 - 95,000; Full time

Benefits offered by this job

152 hours of PTO + 8 paid holidays

Day-one benefits

Job summary

Catalent Pharma Solutions is seeking an Operations Supervisor for the St. Petersburg, FL site. The role emphasizes GMP compliance, quality, and leadership in a 2-2-3 rotating shift pattern and 100% on-site work.

The candidate will oversee SOPs, training, schedules, and cross-functional collaboration with QA, Engineering, and Validation teams to ensure timely batch releases in a compliant, efficient manufacturing environment.

Qualifications

• Bachelor's degree with three years of related experience in the pharmaceutical industry preferred.
• Prior Supervisory experience a plus.
• Training and/or equivalent combination of education and experience will be considered.
• Must be flexible in days of work, able to work 12hour shifts.
• Vision requirements include Ishihara Color Vision Screening and acuity requirements.
• Ability to work under pressure to meet deadlines and lift up to 44 pounds with assistance when needed.

Responsibilities

• Ensure SOP proficiency and verify SOP accuracy; escalate gaps or inconsistencies.
• Monitor on-time completion of operator training requirements.
• Organize and communicate standard and overtime schedules for team members.
• Attend and actively participate in meetings as required.
• Lead and supervise a team of manufacturing operators; define priorities and assignments.
• Monitor production schedules, resource allocation, and workflow to meet batch release timelines.
• Collaborate with QA, Engineering, and Validation teams for compliant operations.
• All other duties as assigned.

Skills

Leadership

GMP compliance

SOPs proficiency

Training oversight

Scheduling

Cross-functional collaboration

Quality mindset

Education

Bachelor's degree in related field

Job description

Catalent Pharma Solutions is seeking an Operations Supervisor for the St. Petersburg, FL site. The role emphasizes GMP compliance, quality, and leadership in a 2-2-3 rotating shift pattern and 100% on-site work.

The candidate will oversee SOPs, training, schedules, and cross-functional collaboration with QA, Engineering, and Validation teams to ensure timely batch releases in a compliant, efficient manufacturing environment.