Gxpcapa Program Manager

Team,

Please prioritize local candidates or candidates located near Greenville, NC, who can work onsite from Day 1, five days a week.

Position Details:

• Role: GXPCAPA Program Manager
• Location: Greenville, NC
• Work Arrangement: 100% Onsite 5 Days a Week
• W2 Rate: $55 60/hr
• C2C Rate: $65 70/hr

Important:

• Submit only local or nearby candidates.
• Candidates must be comfortable working onsite from Day 1.
• Confirm the candidate's willingness to commute to Greenville, NC, before submission.
• Prioritize candidates who closely match the job requirements.

Please focus on strong, qualified local profiles and avoid submitting remote-only candidates.

Must Have skills:
GXP, CAPA, FDA Audit, Lean Six Sigma

Program Manager - GxP CAPA

Remediation Location: Greenville, SC (On-site) Type: Contract

Overview Seeking an experienced Program Manager to lead CAPA remediation workstreams in a regulated pharmaceutical manufacturing environment.

This role will drive cross-functional coordination, track remediation progress, manage risks and dependencies, and ensure timely closure of corrective and preventive actions.

This is a business/domain-focused role and not an IT project management position.

Key Responsibilities

Manage CAPA and remediation activities from planning through closure.

Track actions, milestones, risks, dependencies, and deliverables. Facilitate cross-functional meetings and drive action-item completion.

Coordinate with Manufacturing, Quality, Validation, MSAT, and other site teams. Escalate risks, delays, and resource constraints.

Prepare status reports and updates for leadership and stakeholders. Ensure documentation and remediation traceability align with GxP and quality system requirements. Required Qualifications Experience managing programs/projects in pharmaceutical, biotech, or other regulated manufacturing environments.

Strong knowledge of GxP, CAPA, and quality systems. Proven ability to manage complex, cross-functional remediation initiatives. E

xcellent stakeholder management, communication, and issue-resolution skills. Ability to work on-site in Greenville, SC.

Preferred Experience with audit/inspection remediation and CAPA governance.

Consulting or contract program management experience in manufacturing environments.

Start: Immediate Duration: Based on remediation scope and business needs.