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Sr. Executive QA

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Onsite

Sr. Executive QA

Nitika Pharmaceutical Specialities

Sr. Executive QA

Skills

Testing & QACompliance

2 months ago

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Important information


Contract type:

Permanent

Location:

Nagpur, Maharashtra, India

Work mode:

Onsite

Published on:

27 August 2026

What they need


Roles and Responsibilities :

  • Conduct CAPA investigations to identify root causes of deviations, non-conformities, and out-of-specification results.
  • Develop and implement corrective actions to prevent recurrence of issues in accordance with cGMP regulations.
  • Collaborate with cross-functional teams to resolve quality-related issues and ensure compliance with QMS requirements.
  • Review and approve CAPAs before implementation to ensure they meet regulatory requirements.

Job Requirements :

  • 3-8 years of experience in a pharmaceutical or life sciences industry in a similar role.
  • Strong understanding of GMP/cGMP regulations and their application in a manufacturing environment.
  • Experience with investigation techniques such as FMEA, Fishbones, etc.

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