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Senior Manager – Commercial Quality (India & Saarc)

3-10 years
Not Disclosed
10 Nov. 19, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Senior Manager – Commercial Quality (India & SAARC)

Location: Mumbai, India
Category: Quality

Role Overview

The Senior Manager – Commercial Quality will lead quality operations across India and SAARC markets for the Abbott ID Rapid Diagnostics division. This role is responsible for driving commercial quality excellence, ensuring regulatory compliance, strengthening quality systems, and fostering a quality-focused culture across people, processes, products, and services.

The position requires deep expertise in quality assurance and regulatory frameworks within the medical device, pharmaceutical, diagnostics, or healthcare sectors.


Key Responsibilities

Quality Leadership and Compliance

• Serve as the management representative for Quality and Regulatory compliance, ensuring alignment with Abbott Global Quality and Regulatory Frameworks.
• Build and sustain a robust quality culture across commercial operations.
• Maintain, evaluate, and enhance the Quality Management System (QMS) to ensure compliance and business effectiveness.
• Represent commercial leadership for quality-related decisions including escalations, field actions, and critical product quality matters.

Quality Operations and Monitoring

• Oversee quality complaint management, ensuring timely investigation, resolution, closure, and customer communication while partnering with Legal Manufacturers and Technical Support teams.
• Review product complaint trends and address recurring issues promptly.
• Support Field Corrective Actions (FCA) arising from global or regional safety notifications.
• Provide quality support for Post-Market Surveillance (PMS) activities to prevent supply interruptions.
• Facilitate Corporate Quality Audits, Regulatory Audits, and ISO Notified Body audits.

System Enhancements and CAPA Management

• Ensure effective CAPA implementation across operational sites.
• Lead Supplier Qualification Programs, including evaluation, audits, monitoring, maintenance, and requalification.
• Review and approve changes, deviations, investigations, complaints, and CAPA actions.
• Oversee quality operational budgeting.
• Conduct QMS gap analysis against Abbott standards, prepare remediation plans, and drive compliance improvements.

Product Quality Oversight

• Manage Quality Control activities for imported products distributed in the market.
• Hold final decision-making authority for product release and field corrective actions.
• Evaluate product quality data and escalate concerns to senior management with timely written reports.

Quality System Administration

• Ensure compliance with core quality system requirements such as document control, record management, training, CAPA, risk management, and internal audits.
• Drive sustained compliance with Abbott quality standards and regulatory expectations.
• Coordinate cross-functional activities to resolve product issues and implement containment, mitigation, and corrective actions.

Governance and Performance Monitoring

• Coordinate Quality Management Review meetings, including reporting of quality objectives, escalation of QMS issues, and closure of previous action items.
• Oversee site quality metrics, including tracking, trending, and reporting of key performance indicators.
• Lead internal and external audits/inspections and manage all commercial audit activities in collaboration with commercial office leaders.

Team Development and Talent Management

• Strengthen quality capabilities across the India & SAARC cluster.
• Implement talent strategies to develop a high-performing quality team.
• Promote global mindset, cultural understanding, and cross-regional collaboration.

Additional Responsibilities

• Optimize processes to ensure compliance with entity, business unit, divisional, corporate, and regulatory standards.
• Perform other quality and compliance duties as assigned.


Qualifications

Education

• Bachelor’s degree in Pharmacy, Science, or Engineering.

Experience Required

• Minimum 10 years of experience in Quality Assurance and/or Compliance within a regulated industry.
• Minimum 7 years of industry experience in Medical Devices, Pharmaceuticals, In-Vitro Diagnostics, or Healthcare.
• Minimum 3 years of supervisory or managerial experience.
• Strong proficiency in English communication.


Core Competencies

• Proven leadership and influence across matrixed teams.
• Strong analytical, communication, decision-making, and stakeholder negotiation skills.
• Ability to manage multiple priorities and consolidate insights from diverse business units.
• Exceptional attention to detail and accuracy.
• Ability to work effectively in dynamic, multi-cultural, and geographically dispersed environments.
• Expertise in medical device industry regulations, quality systems, and compliance requirements.
• Experience conducting and managing audits and inspections.