What are the responsibilities and job description for the Quality Event Investigator – Deviation & CAPA position at JMD Technologies Inc.?
Title: Quality Event Investigator – Deviation & CAPA
Location: Greater Framingham Area, MA (Onsite)
Employment Type: Contract
Status: Accepting Candidates
About the role
Support the CMC organization by leading quality events, deviations, investigations, and CAPAs from initiation through closure. Drive root cause analysis, product impact assessments, and CAPA effectiveness while ensuring GMP and internal quality requirements are met.
Key Responsibilities
- Lead end-to-end quality event and deviation investigations through closure.
- Conduct root cause analysis and assess product/process impact with cross-functional SMEs.
- Author clear, scientifically sound GMP investigation reports.
- Drive CAPA execution, effectiveness verification, and timely closure.
- Facilitate cross-functional investigations and track investigation timelines.
- Support change controls and data verification activities as needed.
Qualifications
- 5 years of experience in GMP-regulated biotechnology, pharmaceutical, or cell/gene therapy environments.
- Demonstrated experience leading and authoring deviation, investigation, and quality event records.
- Strong knowledge of GMP regulations and quality systems.
- Experience with root cause analysis and CAPA development/effectiveness.
- Strong technical writing, project management, and organizational skills.
- Experience with eQMS platforms such as Veeva Quality, TrackWise, MasterControl, or similar.
Compensation (MA Pay Transparency):
- Estimated hourly range: $50/hr (W-2).
- Final rate within this range will be based on skills, experience, and interview results.
Salary : $50