Senior Director, Post Market Surveillance

Posted 3 Days Ago
Be an Early Applicant
Veerthala, Nagar, Bharatpur, Rajasthan, IND
In-Office
Senior level
Healthtech • Other • Biotech
The Role
Lead global post-market surveillance, vigilance, and regulatory compliance for medical devices. Own PMS strategy, signal detection, global vigilance reporting, recalls, HHEs, and post-market reporting deliverables while partnering cross-functionally to drive corrective actions and regulatory interactions.
Summary Generated by Built In

Work Shift:

DAY

Work Schedule:

Why Merit?

At Merit Medical, our mission is to create innovative medical devices that improve lives. Our goal is to hire and develop people who want to build something special through hard work, team effort, and commitment. Together, we are making a difference in the lives of patients around the world.

ESSENTIAL FUNCTIONS PERFORMED

  • Provides leadership to establish and sustain the global vision, strategic direction, and long-term roadmap for post market surveillance, vigilance, and regulatory compliance across the organization.
  • Serves as the executive authority for post market surveillance decisions, escalations, and regulatory interactions.
  • Ensures globally harmonized processes, systems, procedures, and decision pathways are aligned with ISO 13485, FDA QSR, and EU MDR Owns and evolves PMS processes, ensuring alignment with corporate objectives and regulatory expectations.
  • Ensures robust complaint trending, signal detection, and escalation processes.
  • Oversees global vigilance reporting (EU MIRs, FDA MDRs, Health Canada, MHRA, TGA, PMDA).
  • Leads cross-functional recall team(s) and ensures global alignment across product platforms and ensures timely closure.
  • Maintains global recall readiness and crisis response governance.
  • Directs the global HHE process, ensuring scientifically sound, risk-based assessments.
  • Provides executive oversight for EU MDR post market reporting deliverables, including PSURs, PMSRs, and trend analyses.
  • Partners with Operations, R&D, and Quality to drive systemic improvements based on data insights.
  • Serves as the executive interface with OEM partners on safety, quality events, and systemic corrective actions.
  • Ensures timely response and closure of OEM SCARS.
  • Influences senior leadership and cross functional stakeholders through data driven insights and strategic recommendations.
  • Performs other duties, as required.

ESSENTIAL PHYSICAL/ENVIRONMENTAL DEMANDS

  • Lifting -- Not to exceed 50 lbs. -- local practice may apply.
  • Writing
  • Sitting
  • Standing
  • Bending
  • Visual acuity
  • Color perception
  • Depth perception
  • Reading
  • Field of vision/peripheral

SUMMARY OF MINIMUM QUALIFICATIONS


•           Education equivalent to a Bachelor’s degree in engineering, life sciences, or related field; advanced degree preferred.

•           A minimum of fifteen (15) years of experience in sales with eleven (11) years in a leadership position in medical device post market surveillance, vigilance, or quality roles.

•           Deep expertise in EU MDR, FDA QSR, ISO 13485, MDSAP, and global vigilance requirements.

•           Demonstrated success leading global teams.

•           Proven ability to manage complex global processes and regulatory interactions.

•           Ability to work across all levels of management and employees to identify and resolve issues.

•           Ability to work well as part of Global Quality team to accomplish organizational objectives effectively. 


COMPETENCIES


•           Leadership

•           Oral and written communication

•           Interpersonal skills

•           Data analysis

•           Problem solving

•           Project management

•           Analytical Skills


COMMENTS


Infectious Control Risk Category II:


The risk category explains whether or not employees are likely to come into contact with blood or body fluids while performing their jobs.  Risk category II states employment and procedures that may require exposure.

As an eligible Merit employee, you can expect the following:

* Multiple Shifts and Hours to choose from: Days, Swing (Eve), and Nights

* Medical/Dental & Other Insurances (eligible the first of month after 30 days)

* Low Cost Onsite Medical Clinic

* Two (2) Onsite Cafeterias

* Employee Garden | Gardening Classes

* 3 Weeks' Vacation | 1 Week Sick-Time | Paid Holidays

* 401K | Health Savings Account

To see more on our culture, go to www.merit.com/careers.

Military Veterans are encouraged to Apply.

Merit is a proud Utah Patriot Partner committed to hiring our Veterans.

Skills Required

  • Bachelor's degree in engineering, life sciences, or related field (advanced degree preferred).
  • Minimum of 15 years of experience with 11 years in leadership in medical device post market surveillance, vigilance, or quality roles.
  • Deep expertise in EU MDR, FDA QSR, ISO 13485, MDSAP, and global vigilance requirements.
  • Demonstrated success leading global teams.
  • Proven ability to manage complex global processes and regulatory interactions.
  • Ability to work across all management levels to identify and resolve issues.
  • Ability to work effectively as part of a Global Quality team to meet organizational objectives.
  • Advanced degree (Masters/PhD) in relevant field.

Merit Medical Systems, Inc. Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Merit Medical Systems, Inc. and has not been reviewed or approved by Merit Medical Systems, Inc..

  • Healthcare Strength An on‑site medical clinic at headquarters and campus wellness initiatives aim to make care more convenient and affordable for employees and families. Safety training and ongoing wellness programming further reinforce the health offering.
  • Retirement Support A 401(k) Profit Sharing Plan with active employer contributions and discretionary matching provides structured support for long‑term savings. Eligibility and plan participation are clearly established for U.S. employees.
  • Equity Value & Accessibility An employee stock purchase plan with a purchase discount enables accessible ownership participation. A successor plan is slated to replace the legacy program, pending shareholder approval.

Merit Medical Systems, Inc. Insights

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The Company
HQ: South Jordan, UT
5,001 Employees
Year Founded: 1987

What We Do

As a global healthcare company, we understand customer needs and innovate and deliver medical solutions that transform patient care. Founded in 1987, Merit Medical Systems, Inc. is engaged in the development, manufacture, and distribution of proprietary disposable medical devices used in interventional, diagnostic, and therapeutic procedures, particularly in cardiology, radiology, oncology, critical care, and endoscopy. Merit serves client hospitals worldwide with a domestic and international sales force and clinical support team totaling in excess of 300 individuals. Merit employs approximately 6,000 people worldwide with facilities in South Jordan, Utah; Pearland, Texas; Richmond, Virginia; Malvern, Pennsylvania; Rockland, Massachusetts; Aliso Viejo, California; Maastricht and Venlo, The Netherlands; Paris, France; Galway, Ireland; Beijing, China; Tijuana, Mexico; Joinville, Brazil; Markham, Ontario, Canada; Melbourne, Australia; Tokyo, Japan; Reading, United Kingdom; Johannesburg, South Africa; and Singapore.

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