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Otsuka Pharmaceutical

Quality Assurance Specialist - Nutraceutical Products

Otsuka Pharmaceutical

Ahmedabad, Gujarat, India
Full-Time
Posted 22 days ago

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Job Description & Responsibilities

Roles and Responsibilities

  • To develop and implement comprehensive quality assurance procedures specific to enteral nutrition products.
  • To ensure compliance with relevant regulations and industry standards in all aspects of enteral nutrition.
  • To monitor and ensure compliance at Contract Manufacturing Operations through continuous document verification and periodic audits.
  • To oversee the evaluation and testing of enteral nutrition products for safety, efficacy, and quality.
  • To monitor product performance through data analysis, quality metrics, and prepare reports for management.
  • To evaluate and manage change control processes to ensure that all modifications in products or processes are assessed for quality impact.
  • To review, approve, and update Standard Operating Procedures (SOPs) related to enteral nutrition and CMO to ensure compliance and operational efficiency.
  • To provide technical responses to queries raised by the Ministry of Health, ensuring accurate and timely information is communicated.
  • To facilitate and participate in meetings with stakeholders to discuss quality assurance matters, product updates, and compliance issues.
  • To conduct internal audits and ensure compliance with quality standards, regulatory requirements, and industry best practices.
  • To manage all product CMO activities and release the batches manufactured at CMO sites.
  • To manage all products derived by Otsuka as per business requirements.
  • To undertake any additional responsibilities assigned by senior management that support quality assurance objectives.

Job Requirements

  • 8-13 years of experience in Quality Assurance Specialist role within the pharmaceutical industry.
  • Strong understanding of regulations governing contract manufacturing, third party manufacturing, and nutraceuticals.
  • Proven expertise in auditing, document verification, data analysis, and implementing corrective actions.

Job Details

Employment TypeFull-Time
Work ModeOn-Site
Experience8 – 13 years
Positions1

Posted by

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Posted on:

7 Oct 2026

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