N
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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