B Pharm Job Opportunity at Sava Healthcare | Executive / Sr Executive – QA Role
Looking for a Pharma QA Job after B.Pharm? A pharmaceutical manufacturing company in Indore is hiring Executive/Senior Executive – Quality Assurance (QA) professionals. This B. Pharm. job opportunity is suitable for candidates with experience in validation, qualification, IPQA, and GMP-regulated pharmaceutical operations.
- Job Title: Executive / Senior Executive – QA (Validation/Qualification/IPQA/Lab QA)
- Location: Indore, Madhya Pradesh, India
About the Company
This Pharma QA Job provides an opportunity for B Pharm professionals to work in a regulated pharmaceutical manufacturing environment focused on quality systems, validation activities, and GMP compliance. The organization offers exposure to pharmaceutical operations, regulatory standards, and quality assurance practices that support safe and effective medicine manufacturing.
Job Description
This B Pharma Job involves managing key Pharma QA Job responsibilities related to validation, qualification, documentation, and regulatory compliance. The Executive/Senior Executive – QA will support process validation, cleaning validation, equipment qualification, and computer system validation activities while ensuring adherence to GMP and global quality standards.
Key Responsibilities
- Execute and review validation activities including process validation, cleaning validation, and equipment qualification.
- Prepare and review validation protocols, reports, and GMP documentation.
- Coordinate with Production, QC, Engineering, and other departments for validation activities.
- Perform risk assessments and gap analysis as per quality requirements.
- Develop cleaning validation protocols, sampling plans, and validation reports.
- Review analytical data and maintain cleaning validation records.
- Support IQ, OQ, and PQ activities for equipment, utilities, and systems.
- Prepare and review CSV documents including URS, RA, IQ/OQ/PQ protocols.
- Ensure compliance with GMP, 21 CFR Part 11, GAMP 5, and data integrity requirements.
- Maintain audit-ready documentation and support regulatory inspections.
Eligibility Criteria
- Education: B Pharm, M Pharm
- Experience: 2–6 years of experience in pharmaceutical QA, validation, or regulated manufacturing environments.
- Knowledge of GMP, ICH, WHO, USFDA, and regulatory guidelines.
- Experience in process validation, cleaning validation, equipment qualification, or CSV is preferred.
Required Skills
- Pharma Quality Assurance (QA)
- GMP Compliance
- Process Validation
- Cleaning Validation
- Equipment Qualification (IQ/OQ/PQ)
- Computer System Validation (CSV)
- Quality Documentation
- Regulatory Compliance
- Data Integrity Principles
- Risk Assessment
- Audit Preparation
- Cross-functional Coordination



