Post Market Regulatory Affairs Specialist

LanceSoft Inc

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West Chester, PA, us on site Until 8/22/2026 First posted March 27, 2025 Last posted March 27, 2025
Job description

EXPERIENCE:
- Ability to work in a cross-functional matrix environment
- Active listening/phone skills
- Collaboration and teaming skills
- Critical thinking skills
- Detail orientation
- Organization skills
- Prioritization and multi-tasking skills
- Strong verbal and written communication skills
- Knowledge of basic medical terminology
- Proficiency in MS Office (Word, Excel, Outlook, PowerPoint, Sharepoint)
- Continuous learner
- Global mindset
- Accountability for own work
- Problem solving/root cause analysis skills 

Job Description:
Responsible for supporting Post Market Regulatory Affairs activities associated with complaint handling and MDR submissions. These activities include intake, investigation, documentation, follow-up, regulatory reporting and metrics. The Regulatory Specialist is responsible for oversight and direct support of technical evaluations and investigation tasks required for complaint processing/closure. The Customer quality Specialist works collaboratively with Quality, Engineering, Manufacturing, Product Development and other functional experts.

DUTIES:
- Responsible and accountable for on-time submission and accuracy of regulatory reports
- Review and complete determination associated Medical Device Report and/or Vigilance Report
- Knowledge of and familiarity with global regulations for reporting
- Directly interface with service centers, Hospitals, Surgeons, and Internal employees for reporting of complaints and adverse events.
- Interact positively with internal, external business partners and colleagues
- Adhere and comply to work instructions, standard operating procedures, and regulations.
- Expedite investigations by collaborating with internal/external business partners
- Achieve productivity targets
- Achieve accuracy targets for complaint documentations
- Participate in projects and events
- Complaint determination
- Reportability assessments
- Conduct follow-ups with complainant, reporters
- Checking your own work
- Updating SharePoint
- Tracking complaints in the process for closure
- All other duties assigned

EDUCATIONAL REQUIREMENTS:
- Bachelor’s degree or equivalent experience
- Generally requires 2 -4 years of related work experience
- RAC or ASQ certification a plus


All your information will be kept confidential according to EEO guidelines.

About this role

Summary

Support complaint handling, MDR submissions, investigations, and regulatory reporting in medical devices.

Job title

Post Market Regulatory Affairs Specialist

Experience level

2-4 years

Industry

medical devices

Location requirements

West Chester, PA, US; remote not specified

Salary

Not specified

Management role

No

Skills & keywords

Required skills

medical terminologyregulatory reportingcomplaint handlinginvestigationMS Office

Preferred skills

RACASQ certification

Specializations

complaint handlingMDR submissionsmedical terminologyregulatory reporting
Locations

Structured locations inferred from the posting.

West Chester, PA, USA

On-site City