Quality Assurance Project Manager
Holly Springs, NC
Job Id:
141896
Job Category:
Job Location:
Holly Springs, NC
Security Clearance:
No Clearance
Business Unit:
Piper Companies
Division:
Piper Enterprise Solutions
Position Owner:
Anne Green
Piper Companies is hiring a Quality Assurance Project Manager for a Biopharma company located in Holly Spring, NC. The Quality Assurance Project Manager will focus on resource forecasting, data-driven capacity planning, and strategic collaboration between CQV teams and PMO to ensure seamless execution of project quality deliverables. The Quality Assurance Project Manager will need to sit on site in Holly Springs, NC 5 days per week, this role is not able to provide sponsorship and is a long term open ended contract.
Responsibilities for the Quality Assurance Project Manager:
- Act as a liaison between CQV and PMO teams, ensuring effective communication of project quality requirements.
- Analyze resource demands using data-driven metrics and reporting tools to optimize personnel capacity.
- Collaborate with cross-functional teams to enhance QA processes and compliance standards in biopharma projects.
- Establish and maintain tracking systems to monitor progress, risks, and corrective actions related to QA deliverables.
- Support continuous improvement initiatives within Quality Assurance and Project Management functions.
Requirements for the Quality Assurance Project Manager:
- 2–5 years of project management experience within pharma/biopharma sectors.
- Proficiency in forecasting and reporting resource metrics, with experience in data-driven decision-making.
- Previous experience working within a PMO is a plus.
- PMP Certification Preferred
Compensation for the Quality Assurance Project Manager:
- $50.00 - $70.00 per hour
- Full Comprehensive Benefits: Heath, Vision, Dental, PTO, Paid Holiday, Sick leave if required by law
Keyword: Project Manager, Quality Assurance, Biopharma, Pharma, CQV, PMO, Resource Forecasting, Capacity Planning, Data Metrics, Regulatory Compliance, Project QA, GMP, FDA Regulations, Cross-functional Collaboration, Reporting Tools, Personnel Demand, Risk Management, Continuous Improvement, Stakeholder Communication, Manufacturing Quality, Process Optimization, Project Execution, KPI Tracking
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This job opens for applications on 5/16/2025. Applications for this job will be accepted for at least 30 days from the posting date.