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Advanced Analytics Analyst

Medtronic
Mumbai2-7 LPA Posted 24 Jun 2025
FULL TIME
Qms
Healthcare
Pharma
Data Analysis
Iso 13485
+4 more

Job Description

A Day in the Life In this role, this role will partner with Quality System team members to generate, analyze, communicate, and follow up with stakeholders to actions related to standard reports for the following QMS processes:

-Periodic Review of QMS procedures

-Training coming due and/or overdue notifications

-Quality Data Analysis (QDA)

In addition, this role will assist in the retrieval, review, and archival of Allograft Tissue Tracing Records.

Responsibilities may include the following and other duties may be assigned:

Communicates and collaborates with internal stakeholders such as Quality, R&D, Regulatory, Operations, Service and Repair, Supplier Quality, Procurement, Operations Quality, and Program Management Office across the following CST QMS entities:

o Boxborough

o Caesarea

o Fort Worth CSF

o Fort Worth MPSS

o Lafayette

o Memphis Pyramid

o Memphis SGT

Generates and analyzes standard reports (e.g., Periodic Review, Training and Quality Data Analysis) for compliance with KPIs, identification of patterns of underperformance to KPIs

Communicates coming due and/or overdue notifications for Training and Periodic Reviews to affected personnel, their management, and Quality leadership

Coordinates with internal stakeholders to implement corrections to Agile MAP with regards to Document and Process Owners

Coordinates with internal stakeholders to implement corrections to Cornerstone with regards to removal of unnecessary trainings

Coordinates with Quality System Program Manager on the generation of standard reports for QDA, preparation of presentations, coordination with data providers and reviewers, and processing of records within Agile MAP

Required Knowledge and Experience

Bachelor degree; Engineering or Science degrees preferred

3+ years quality assurance experience in medical or pharmaceutical industry

Familiarity with medical device Quality Management System requirements (e.g., US 21 CFR Part 820, ISO 13485:2016, Regulation (EU) 2017/745)

Experience running data queries and reports in software applications

Strong verbal and written communication skills and ability to work in a team oriented environment

Agile PLM knowledge/experience

Ability to work independently once trained

Ability to be proactive and lead initiatives

Ability to multitask.

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