PHARMAFull-time
Chemist – IPQR
INDORE (IN)ONSITEPOSTED: 8/6/2026
PHARMAFull-time
HIRING ORGANIZATIONIPCA LABORATORIES LIMITEDTechnology

ROLE DEFINITION & RESPONSIBILITIES
Company: Ipca Laboratories Limited • Department: Quality Assurance (QA) • Position: Chemist – IPQR • Employment Type: Full-Time • Industry: Pharmaceuticals • Qualifications: B.Pharm, M.Pharm, B.Sc, M.Sc, Other relevant Life Sciences qualifications • Experience Required: Minimum 2 Years, Maximum 3 Years • Experience in pharmaceutical Quality Assurance functions is mandatory. • Responsibilities: - Conducting In-Process Quality Review activities. - Verification of batch manufacturing and packaging records. - Ensuring compliance with cGMP and SOP requirements. - Documentation review and quality investigations. - Monitoring manufacturing processes for quality compliance. - Supporting internal and external audits. • Required Skills: IPQR knowledge, Pharmaceutical Quality Assurance, GMP & cGMP Compliance, Documentation Management, SOP Review and Preparation, Regulatory Compliance, Audit Readiness, Quality Systems Management, Data Analysis and Reporting, Pharmaceutical Manufacturing Processes. • Why Join Ipca Laboratories: - Work with a reputed pharmaceutical organization. - Exposure to advanced quality systems and regulatory practices. - Professional growth opportunities within Quality Assurance. - Collaborative and compliance-driven work environment. - Opportunity to contribute to pharmaceutical quality excellence.
REQUIRED VERIFIED SKILLS
IPQR
Pharmaceutical Quality Assurance
GMP
cGMP
Documentation Management
SOP Review
Regulatory Compliance
Audit Readiness
Quality Systems Management
Data Analysis
Pharmaceutical Manufacturing Processes
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Salary was not disclosed. Compensation is expected to be competitive with industry standards for Quality Assurance professionals having 2–3 years of pharmaceutical manufacturing experience.
ORGANIZATION CONTEXT & CULTURE
Ipca Laboratories Limited is actively hiring for this position.
INDUSTRY: Technology
EXPECTED CAREER ROADMAP
This position provides a strong foundation for advancement into senior QA, manufacturing quality, compliance, validation, and regulatory affairs roles within the pharmaceutical industry.
APPLICATION ADVISORY
Emphasize IPQR experience, batch record review, GMP compliance, SOP adherence, audit support, documentation accuracy, and quality investigation exposure. Demonstrate experience in pharmaceutical manufacturing quality processes.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
Verify your capability profile and matching credentials before submitting direct applications.
