Looking to make a meaningful impact in healthcare My client is seeking a Senior Analyst to lead critical regulatory and quality initiatives that directly support lifesaving medical technologies. This is your chance to step into a highvisibility role that blends strategic oversight with handson execution all in support of advancing patient care on a global scale.
Why You Should Apply
- Join a company making a global difference in critical care and patient outcomes
- Step into a highly crossfunctional role with exposure across quality regulatory and product teams
- Lead and own key functions including supplier quality and complaint systems
- International travel opportunities for supplier audits
- Competitive benefits and strong internal support systems
What Youll Be Doing
- Maintain and enhance ISO 13485 and MDSAPcompliant Quality Management Systems
- Represent the company during audits and inspections from FDA and international agencies
- Manage supplier quality including conducting and reporting on audits
- Own the customer complaint process from investigation to trend reporting
- Lead risk management activities including FMEAs and regulatory assessments
- Prepare review and submit technical documentation and regulatory filings
About You
- Be able to do the job as described
- Experienced in handling complaints supplier quality programs and risk management for medical devices
- Adept in fastpaced lean environments with overlapping priorities
- Strong critical thinking time management communication and writing skills
- Independent and adaptable with a proactive approach to complex regulatory challenges
How To Apply
Wed love to see your resume but we dont need it to have a conversation. Send an email to and tell me why youre interested. Or if you do have a resume ready apply here.
Required Experience:
Senior IC