Join Takeda’s Legacy of Excellence in Quality Assurance-Apply before 30th May 2025

Takeda Pharmaceuticals

Website Takeda Pharmaceuticals

About Takeda Pharmaceuticals

With a legacy spanning over 240 years, Takeda is a global, research-driven biopharmaceutical leader committed to translating science into life-changing treatments. Our relentless pursuit of innovation has helped deliver therapies that have transformed patient care worldwide. Join us in shaping the future of healthcare through quality and integrity.


Position Overview

  • Job Title: Senior Executive / Executive – Quality Assurance

  • Department: Quality Assurance

  • Experience Required: 6 to 8 years (preferably in API Manufacturing)

  • Work Location: Mumbai, Maharashtra

  • Application Deadline: 30th May 2025

  • Industry Type: Pharmaceuticals / Healthcare / Clinical Research


Key Responsibilities

  • Perform real-time monitoring of production activities to ensure compliance with cGMP and internal quality standards.

  • Conduct routine inspections and in-process checks to confirm adherence to batch specifications and standard protocols.

  • Identify and document deviations, OOS/OOT results, and non-conformances, ensuring timely implementation of CAPA.

  • Review Batch Manufacturing Records (BMRs), analytical data, and other key documents for completeness and accuracy.

  • Participate in the review and execution of validation and qualification protocols.

  • Support internal audits and regulatory inspections, contributing to ongoing GMP compliance.

  • Collaborate with production and quality control teams to resolve quality concerns efficiently.

  • Train production staff on quality procedures, regulatory requirements, and documentation best practices.

  • Develop and maintain quality documentation including SOPs, batch records, and logbooks.


Candidate Requirements

  • Education: M.Pharm / B.Pharm / M.Sc from a recognized institution.

  • Strong working knowledge of GMP, FDA guidelines, and ICH/cGMP standards.

  • Experience in API manufacturing and IPQA (rotational shifts) is highly preferred.

  • Proficient in using quality management tools such as SAP, TrackWise, etc.

  • Excellent attention to detail, documentation accuracy, and observation skills.

  • Proven teamwork, decision-making, and problem-solving abilities.

  • Ability to manage multiple responsibilities in a dynamic, regulated environment.


Why Takeda?

  • Be a part of a globally respected and innovation-led company.

  • Contribute to cutting-edge pharmaceutical development and patient-centered solutions.

  • Experience a culture of integrity, collaboration, and continuous improvement.

  • Access career development opportunities within a global network.


📨 Apply by 30th May 2025 to take the next step in your QA career with a company that values quality, people, and purpose.


To apply for this job please visit jobs.takeda.com.