Analysis Skills, Biotech and Pharmaceutical, Corrective and Preventative Action (CAPA) Systems, Cross-Functional, Data Analysis, GMP (Good Manufacturing Practices), Investigative Reports, Laboratory, Legal, Metrics, Quality Assurance, Quality Control, Quality Management, Quality Metrics, Reporting Skills, Root Cause Analysis, Technical Writing, Time Management, Trend Analysis, Writing Skills
Piper Companies is seeking a Deviation Investigator to support a global pharmaceutical organization in Titusville, NJ. The Deviation Investigator will support laboratory investigations, deviation management, and quality metrics reporting within a GMP-regulated environment.
Responsibilities of the Deviation Investigator:
- Lead deviations and investigations from initiation through closure
- Perform root cause analysis and support CAPA activities
- Collaborate with QA, QC, and cross-functional teams to drive timely investigation outcomes
- Author investigation reports and technical documentation
- Support metrics tracking, trending, and reporting using Excel and quality systems
Qualifications of the Deviation Investigator:
- 3+ years of experience in a GMP-regulated pharmaceutical or biotechnology environment
- Experience with investigations, deviations, CAPAs, or quality systems
- Knowledge of root cause analysis methodologies
- Strong technical writing, data analysis, and Excel skills
- TrackWise or similar quality management system experience preferred
- B.S. in a scientific discipline preferred
Compensation for the Deviation Investigator:
- Pay Rate: $35/hr.
- Long-term Contract Opportunity
- Onsite in Titusville, NJ
- Comprehensive Benefits: Medical, Dental, Vision, 401K, PTO, Sick Leave (as required by law), and Paid Holidays
Keywords: Deviation Investigator, CAPA, Investigations, Root Cause Analysis, GMP, Quality Systems, TrackWise, QC Compliance, Pharmaceutical
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