Pharma Development & Clinical Manufacturing Supervisor

Catalent Pharma Solutions; Greenville (NC); On-site; USD 90,000 - 130,000; Full time

Benefits offered by this job

Medical, dental, and vision benefits

Tuition Reimbursement

Paid time off and holidays

Career growth opportunities

Diversity and inclusion programs

Wellness programs and onsite fitness

Job summary

Catalent Pharma Solutions in Greenville, NC, is seeking a seasoned supervisor to lead Pharmaceutical Development and Clinical Manufacturing operations, ensuring safe, right‑first‑time production in support of oral solid dose programs.

You will supervise batch records, coach staff, and coordinate cross‑functional teams to meet project timelines while upholding cGMP, safety, and quality systems; this is an onsite role, Monday–Friday.

Qualifications

• Bachelor’s degree plus 5+ years in pharmaceutical development or clinical manufacturing.
• Ability to lead teams in a regulated environment with staff development.
• Ability to lift >40 lbs and perform physical requirements.

Responsibilities

• Plan, coordinate, and supervise Pharmaceutical Development and Clinical Manufacturing activities, including development, clinical, engineering, registration‑support, and scale‑up batches.
• Lead daily production execution to ensure batch records, protocols, logbooks, forms, procedures, and other controlled documents are completed accurately, contemporaneously, and in accordance with cGMP and Catalent data integrity expectations.
• Provide direct supervision, coaching, training, and performance support for production team members to promote safe, compliant, and consistent execution.
• Coordinate daily priorities with cross‑functional site teams to support project timelines, client commitments, production readiness, and effective communication.
• Ensure manufacturing suites, equipment, materials, and documentation are maintained in a state of readiness and compliance with site procedures, safety standards, quality expectations, and regulatory requirements.
• Supervise equipment set‑up, changeover, cleaning verification, material staging, line clearance, area readiness, batch execution, in‑process sampling, and post‑run documentation.
• Support development, engineering, qualification, process characterization, cleaning, and validation protocols, including reliable collection and submission of required samples and supporting records.
• Other duties as assigned

Skills

Leadership

Regulatory compliance

cGMP knowledge

Cross-functional collaboration

Safety training

Education

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

Associate degree in related discipline

High school diploma with related experience

Job description

Catalent Pharma Solutions in Greenville, NC, is seeking a seasoned supervisor to lead Pharmaceutical Development and Clinical Manufacturing operations, ensuring safe, right‑first‑time production in support of oral solid dose programs.

You will supervise batch records, coach staff, and coordinate cross‑functional teams to meet project timelines while upholding cGMP, safety, and quality systems; this is an onsite role, Monday–Friday.