QA Supervisor – Pharma Quality & Process Excellence

Catalent Pharma Solutions; Pennsylvania; On-site; USD 90,000 - 120,000; Full time

Benefits offered by this job

152 hours PTO + 8 paid holidays

Tuition Reimbursement

Medical, dental and vision benefits

Wellness programs

Job summary

Catalent Pharma Solutions in Philadelphia, PA, seeks an experienced QA professional to oversee incoming, distribution, and destruction audits and to ensure compliance with cGMP and GDP in a fast-paced production environment.

The role partners with Supply Chain and Operations, leading investigations, tracking metrics, and driving continuous improvement while aligning with regulatory requirements and company SOPs.

Qualifications

• HS Diploma/GED required with 5+ years of Production QA experience.
• College degree (BA/BS) preferred.
• Proven track record monitoring/auditing quality and identifying efficiencies in production.

Responsibilities

• Responsible for QA activities related to incoming, distribution and destruction and process auditing.
• Assist in ensuring quality and identity of pharmaceutical products during all aspects of incoming, distribution, or packaging processes.
• Act as Quality partner to support Supply Chain and Operations.
• Enforce Catalent policy and regulatory requirements.
• Act as site SME for Good Manufacturing Practices and Good Distribution Practices.
• Schedule daily resource plan to support Supply Chain/Operations activities.
• Lead investigations for compliance issues regarding incoming, distribution, returns, destruction, or packaging/production.
• Develop process excellence and efficiencies prior to project start.
• Track and report metrics and identify trends and predictive models.
• All other duties as assigned.

Skills

QA Auditing

Regulatory compliance

Leadership

Continuous improvement

MS Office

Education

HS Diploma/GED

BA/BS preferred

Tools

Inventory Management system

ERP systems

Reading engineering drawings

Job description

Catalent Pharma Solutions in Philadelphia, PA, seeks an experienced QA professional to oversee incoming, distribution, and destruction audits and to ensure compliance with cGMP and GDP in a fast-paced production environment.

The role partners with Supply Chain and Operations, leading investigations, tracking metrics, and driving continuous improvement while aligning with regulatory requirements and company SOPs.