Job Title: Pharma Investigator
Location: West Point, PA
Duration: 12 Months (Contract)
Education Requirements:
B.S. or B.A. in Engineering, Sciences, or a related discipline
2–4 years of relevant experience (co-op/internship experience acceptable in combination with full-time roles)
Required Experience and Skills:
Strong technical writing abilities
Excellent verbal and written communication skills
Strong leadership and collaboration skills
Proven ability to manage multiple projects and meet deadlines
Preferred Experience and Skills:
Experience in biologics, vaccine, or bulk sterile manufacturing environments
Familiarity with Change Control processes
Experience with Deviation Management and Investigations
Author, update, and lead GMP documentation such as SOPs, batch records, technical protocols, validation documents, and change control documents
Support deviation investigations including impact assessments, root cause analysis, and development of corrective and preventive actions (CAPAs)
Assist in writing investigations and quality incident reports
Provide support for facility, equipment, and continuous improvement projects across sterile supply departments
Analyze complex issues from a broad perspective (compliance, equipment, safety, process, automation, personnel) to identify and resolve root causes
Design and review experimental protocols where needed
Deliver hands-on, floor-level support for resolving technical or operational challenges
Lead or contribute to performance improvement projects to enhance compliance, reduce costs, increase efficiency, or improve Right-First-Time performance
Actively support environmental, safety, and compliance goals
Manage project timelines, escalate risks to deliverables, and develop mitigation plans
Collaborate closely with cross-functional teams, including Quality, Operations, Planning, Engineering, and external partners