Executive Jobs | Vantive is Hiring Sr Executive |
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Looking to step into impactful executive jobs in the medical device industry? This opportunity at Vantive is ideal for professionals seeking stable and growth-oriented life science jobs in quality and compliance. The Sr Executive, Product Surveillance role offers hands-on exposure to post-market surveillance, regulatory reporting, and quality control systems, making it a strong career move for candidates aiming to grow in quality control jobs within global healthcare organizations.
Job Details
- Job Title: Sr Executive, Product Surveillance
- Req No: JR – 192735
- Location: Gurgaon, India
- Job Category: Quality Control
About the Company
Vantive is a global vital organ therapy company with a 70-year legacy in kidney care innovation. The organization is committed to extending lives and improving patient outcomes through advanced therapies and digital solutions. Vantive focuses on quality, compliance, and patient safety across its medical device portfolio. With strong investments in innovation and post-market surveillance, the company continues to lead in regulated healthcare environments. Vantive promotes a purpose-driven and collaborative work culture. A career at Vantive offers meaningful work with global impact in life sciences.
Key Responsibilities
- Evaluate potential product quality complaints and initiate applicable records & actions within proper Quality System.
- Own and process quality complaint as per applicable procedures.
- Determine, facilitate and/or approves reportability assessments and decisions based on applicable procedures.
- Author and submit applicable regulatory reports (MDR, MIR, etc.) to competent authorities when deemed required.
- Monitor the status and progression of complaints under investigation and initiate actions to facilitate its resolution and closure.
- Review and approve the results of Engineering, Manufacturing, Quality, Service and/or Supplier evaluations and investigations of complaints.
- Performs queries to provide complaint data and ad hoc trend analysis on reported product problems/complaints to drive continuous improvements within the department and organization.
- Implement and maintain Post Market Surveillance documents (PMSP, PSUR, etc.) as per EU Medical Device Regulation.
- Performs other duties as needed and assigned.
Education and Experience
- Bachelor’s Degree – Preferred: engineering, biomedical, life science, or equivalent (S.T.E.M.).
- Prior experience (2+ years) with Regulatory, Quality, Compliance or a combination of technical experience such as analytical development, manufacturing sciences and Quality/Regulatory.
- Experience with current U.S. FDA, EUMDR, MDD, ISO 13485, ISO9001, MDSAP and/or CMDR regulations, standards, and guidance documents (Preferred).
Skills
- Excellent verbal and written communication skills.
- Analytical approach to problem solving.
- Ability to handle and manage workload independently.
- Well organized and able to multitask effectively in a rapid paced environment, as well as show assertiveness, when interfacing with other personnel during the complaint handling process.
- Experience with Trackwise or equivalent complaint tracking system software and Microsoft Office and database skills are required.
- Knowledge of FDA/ ISO regulations and Country requirements.
- Knowledge of MDR and MDV reporting.
This position offers a strong pathway into executive jobs within medical device quality and surveillance. Professionals seeking reliable and impactful life science jobs will benefit from Vantive’s structured quality systems, global regulatory exposure, and patient-centric mission. It is a valuable opportunity for those aiming to build long-term careers in quality control jobs.
