Pharma Dev & Clinical Manufacturing Supervisor

Catalent Pharma Solutions; South Carolina; On-site; USD 110,000 - 140,000; Full time

Benefits offered by this job

Medical, dental, and vision benefits

Tuition Reimbursement

Paid time off and holidays

Onsite fitness facilities and wellness

Job summary

Catalent is seeking a Supervisor for Pharmaceutical Development and Clinical Manufacturing at our Greenville, NC site. You will lead daily operations for oral solid dose development, clinical batches, and scale‑up, ensuring activities are planned, documented, and executed safely, right‑first‑time, and in compliance with cGMP and regulatory standards.

You will mentor production teams, coordinate cross‑functional priorities, and maintain readiness of suites, equipment, and documentation.

Qualifications

• Bachelor’s degree or higher in a related field with pharma development/clinical manufacturing experience.
• Demonstrated success leading teams in a regulated environment and ensuring quality objectives.
• Ability to lift 40 lbs and work in a physical, on-site manufacturing setting.

Responsibilities

• Plan, coordinate, and supervise development and clinical manufacturing activities, including scale-up batches.
• Lead daily production execution ensuring batch records and SOPs meet cGMP and data‑integrity standards.
• Mentor production staff, provide coaching, and support performance development.
• Coordinate priorities with cross‑functional teams to meet timelines and client commitments.
• Maintain readiness of manufacturing suites, equipment, materials, and documentation.
• Oversee equipment set-up, changeover, cleaning verification, and post‑run documentation.
• Support oral solid dose operations and related development or clinical processes as applicable.
• Provide input on equipment needs, containment controls, and process workflows.
• Address safety, material, and documentation issues; support investigations and CAPAs.

Skills

Leadership

Cross-functional collaboration

Regulatory compliance

cGMP knowledge

Team coaching

Safety leadership

Education

Bachelor’s degree in Pharmaceutical Sciences, Engineering, Industrial Technology, Business Administration, Operations

Associate degree + 6 years of experience

High school diploma + 7 years of experience

Job description

Catalent is seeking a Supervisor for Pharmaceutical Development and Clinical Manufacturing at our Greenville, NC site. You will lead daily operations for oral solid dose development, clinical batches, and scale‑up, ensuring activities are planned, documented, and executed safely, right‑first‑time, and in compliance with cGMP and regulatory standards.

You will mentor production teams, coordinate cross‑functional priorities, and maintain readiness of suites, equipment, and documentation.