Role Summary
Quality Systems Co-Op at Haleon. Support site-wide quality systems to ensure compliance with global regulatory standards and internal quality frameworks within the Oak Hill manufacturing facility.
Responsibilities
- Support quality system operations by assisting with documentation control, change control tracking, and CAPA (Corrective and Preventive Actions) processes to ensure compliance with internal standards and regulatory expectations.
- Participate in internal audits and inspection readiness activities, helping to gather evidence, track commitments, and maintain audit documentation in alignment with Good Manufacturing Practices (GMP).
- Assist in data collection and reporting for Periodic Product Reviews (PPRs), helping to identify trends and support continuous improvement initiatives across product lines.
- Collaborate with cross-functional teams to resolve system-related issues and contribute to quality improvement projects, gaining exposure to pharmaceutical quality operations and compliance frameworks.
- Engage in supplier quality and complaint tracking activities, supporting documentation reviews and learning how external quality systems are managed within a regulated environment.
Qualifications
- Pursuing a BS degree in Engineering or Chemistry, Biology, or related field
- Must have an active student status for the duration of the Co-Op
- Must be eligible to work in the US at the time of, and for the duration of, their employment. Employees will be required to furnish evidence of US work authorization
- Must be eligible to work onsite on a full-time basis during the internship duration (40 hours/week) and provide their own funding for relocation and commuting.
Preferred Qualifications
- Basic understanding of working in a GMP (Good Manufacturing Practice) environment.
Location
East Durham, NY
Education
- No additional education requirements beyond degree-related qualifications specified above.