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Head – Tpmqa India - Biosimilars

12 years
Not Disclosed
10 Dec. 8, 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

Head – TPMQA India (Biosimilars)

Location: Mumbai, India
Category: Quality

Role Overview

The Head – TPMQA India (Biosimilars) is responsible for leading Quality Assurance oversight for Third-Party Manufacturers (TPMs) supporting Biosimilar operations across India and the APAC region. This strategic role ensures end-to-end GMP compliance, quality governance, audit readiness, and adherence to Abbott’s global quality standards. The position requires deep expertise in biosimilars manufacturing, QMS implementation, regulatory compliance, and quality risk management.


Primary Job Function

  • Provide comprehensive Quality Oversight for all TPMs supplying Biosimilars in India and APAC.

  • Ensure robust QMS implementation and ongoing GMP compliance at partner manufacturing sites.

  • Maintain inspection readiness for Abbott audits and external regulatory inspections.

  • Manage and review investigations related to product failures, OOS results, deviations, and customer complaints.

  • Review Annual Product Quality Reviews (APQRs) for all relevant Biosimilar products.

  • Enforce adherence to Abbott policies, procedures, and quality systems.


Core Responsibilities

Quality Leadership and Oversight

  • Lead quality operations across all assigned TPM sites, ensuring consistent implementation of GMP standards.

  • Monitor quality performance ratings of TPM sites and drive continuous improvement initiatives.

  • Implement Abbott’s quality strategy and establish site-specific quality plans.

  • Lead quality improvement projects across identified TPM sites.

Regulatory and Compliance Management

  • Ensure compliance with regulatory expectations for labeling, stability studies, documentation, and batch release.

  • Support regulatory submission requirements for Abbott markets and ensure timely completion of quality deliverables.

  • Guarantee complaint investigations are completed within defined timelines with robust root cause analysis.

Quality Systems and QMS Excellence

  • Strengthen QMS maturity at TPM sites, promoting QMS as a management tool across the supply chain.

  • Conduct periodic quality reviews with TPM QA teams to ensure alignment with Abbott’s quality standards.

  • Foster a quality-first culture through targeted training, capability building, and awareness programs.

Change Management and Product Quality

  • Review and approve change controls, exceptions, and FLQR documentation from a QA standpoint.

  • Ensure product supply is released only after required change control approvals.

  • Oversee complaint closure metrics and ensure timely resolution supported by adequate investigations.


Supervisory Responsibilities

  • Direct Reports: 0

  • Indirect Reports: 0


Position Accountability and Scope

  • Assess training needs for TPM teams and support capability building for Biosimilar QA functions.

  • Ensure timely closure of quality complaints and deviations.

  • Maintain accountability for all regulatory and market-aligned documentation.

  • Strengthen quality performance and ensure consistent supply of compliant Biosimilar products.


Qualifications

  • M.Pharm, M.Sc in Biochemistry, Microbiology, or equivalent scientific discipline.


Experience Required

  • Minimum 12 years of professional experience in pharmaceutical Quality Assurance.

  • Experience in the Quality function of a Biosimilars manufacturing site is highly desirable.

  • Strong understanding of GMP, QMS, regulatory compliance, and third-party manufacturing operations.

  • Proven capability in leading quality operations and facilitating audit readiness at partner sites.