IPQA Officer
Nitika Pharmaceutical Specialities · Nagpur · onsite · Posted 61d ago
Up to ₹1.5L PA0–3 yrsfulltimeSourced from
About a minute. You'll make an account on the way through.
About this role
Roles and Responsibilities :
- Ensure compliance with GMP regulations and company policies in the IPQA department.
- Conduct regular audits and inspections to identify areas for improvement and implement corrective actions.
- Develop, review, and maintain SOPs (Standard Operating Procedures) related to documentation, testing, and release of pharmaceutical products.
- Collaborate with cross-functional teams to resolve issues related to product quality, stability, and regulatory compliance.
Job Requirements :
- 0-3 years of experience in a similar role within the pharmaceutical industry.
- Strong understanding of Good Manufacturing Practices (GMP) guidelines and regulations.
- Ability to develop accurate documents such as protocols, reports, and records according to established standards.
Sourced from naukri
Skills
SOPGMPDocumentation
About Nitika Pharmaceutical Specialities

Nitika Pharmaceutical Specialities
Pharma
375
employees
1991
35 years old
Nagpur, Maharashtra
India
Up to ₹1.5L PA
This role
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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