Sr. Executive QA
Nitika Pharmaceutical Specialities · Nagpur · onsite · Posted 55d ago
Undisclosed3–8 yrsfulltimeSourced from
About a minute. You'll make an account on the way through.
About this role
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.
Sourced from naukri
Skills
Audit HandelingCGMPCAPAInvestigationQMSGMP
About Nitika Pharmaceutical Specialities

Nitika Pharmaceutical Specialities
Pharma
375
employees
1991
35 years old
Nagpur, Maharashtra
India
About
Nitika Pharmaceutical Specialities manufactures diverse products across various industries, adapting to technological advancements to remain competitive globally.
Industries
PharmaHealthcare / Pharma
Employee ratings
154 reviews
3.5/ 5
Culture
3.4
Career growth
3.2
Work-life
3.3
Employees rate it well for
Salary17Work Life Balance11Work Culture8Learning8Senior Management7
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