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Manager Qa – Epd Quality Systems

Abbott
Abbott
5-8 years
Not Disclosed
Mumbai, India
10 Feb. 16, 2026
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

Manager QA – EPD Quality Systems
Location: Mumbai, India
Organization: Abbott
Department: Quality
Division: Established Pharmaceuticals Division (EPD)
Employment Type: Full-Time
Job ID: 31139041

Job Overview
The Manager QA – EPD Quality Systems is responsible for managing and strengthening quality system initiatives within the Established Pharmaceuticals Division to ensure the consistent delivery of safe, effective, and high-quality pharmaceutical products. The role focuses on supplier and third-party manufacturer quality oversight, quality system governance, and regulatory compliance in alignment with global business and regulatory standards.

This position plays a critical role in managing quality questionnaires, driving quality improvement initiatives, and supporting cross-functional collaboration to ensure operational excellence and compliance across the organization.

Key Responsibilities

Quality Systems Management and Governance
Manage quality system initiatives in alignment with the EPD Quality System framework and governance standards.
Act as a subject matter expert for assigned quality systems and provide technical guidance to internal stakeholders.
Serve as process owner for designated quality processes, ensuring effective implementation and compliance.
Maintain awareness of current and emerging regulatory requirements and support business unit transitions where required.

Supplier and Third-Party Manufacturer Quality Oversight
Manage the Quality Questionnaire program for suppliers and third-party manufacturers, including scheduling, execution, and monitoring.
Review completed quality questionnaires to ensure accuracy, completeness, and compliance with quality standards.
Collaborate with supplier and third-party manufacturer quality assurance teams for evaluation and timely completion of documentation.
Support supplier quality management processes and ensure alignment with organizational quality expectations.

Documentation and Data Management
Develop and maintain quality documentation, data records, and tracking systems to support efficient document management processes.
Ensure accuracy and consistency of quality records and maintain compliance with documentation control requirements.

Global Quality Initiatives and Collaboration
Lead global quality initiatives and coordinate implementation activities across business units.
Participate in cross-functional quality assurance teams to support compliance, quality improvement, and process optimization initiatives.
Collaborate with internal and external stakeholders to address quality issues and implement corrective actions.

Quality Improvement and Risk Management
Analyze quality data and performance metrics to identify trends and support strategic action plans.
Identify quality issues and implement corrective and preventive actions (CAPA).
Support quality improvement programs, risk management activities, and continuous process enhancement initiatives.

Role Scope and Reporting Structure
Reports to the Senior Manager QA – EPD Quality Systems and Strategy.
No direct or indirect supervisory responsibilities.

Education Requirements
Bachelor’s degree in Chemistry, Pharmacy, Biology, Microbiology, or a related scientific or technical discipline.

Experience Requirements
Minimum 5–8 years of experience in the pharmaceutical or medical device industry with strong exposure to quality systems and regulatory compliance.
Demonstrated experience in supplier quality management, quality system implementation, and quality process improvement initiatives.

Required Skills and Competencies
Strong knowledge of quality system regulations and pharmaceutical compliance standards.
Ability to lead, influence, and collaborate with internal and external stakeholders.
Experience in quality data analysis, metrics trending, and performance monitoring.
Proficiency in Microsoft Office tools including Excel, PowerPoint, Visio, and Adobe Acrobat.
Strong leadership, project management, and problem-solving skills to manage complex quality issues.
Experience in identifying quality risks and implementing corrective and preventive actions.
Excellent written and verbal communication skills in business English.