Quality Assurance Jobs | Savaglobal Chemistry Jobs | Apply Now
Looking for the latest Quality Assurance Jobs in the pharmaceutical industry? Savaglobal is hiring Executive / Senior Executive professionals for its Quality Assurance department. This opportunity is ideal for candidates seeking Chemistry Jobs with experience in validation, qualification, and GMP-regulated manufacturing. If you want to advance your career in pharmaceutical quality systems and compliance, this role offers an excellent opportunity to grow with an industry-focused organization.
About the Company:
Savaglobal is committed to supporting pharmaceutical organizations by connecting skilled professionals with rewarding career opportunities. With a strong emphasis on quality, regulatory compliance, and operational excellence, the company helps build successful careers across the pharmaceutical sector. Professionals pursuing Chemistry Jobs through Savaglobal gain opportunities to work in quality-driven environments while contributing to high manufacturing and compliance standards.
Job Overview:
Savaglobal is hiring Executive / Senior Executive professionals for the Quality Assurance department at its Indore manufacturing facility. These Quality Assurance Jobs are suitable for candidates with 2–6 years of experience in validation and qualification activities within regulated pharmaceutical manufacturing. The role involves process validation, cleaning validation, equipment qualification, computer system validation, documentation, regulatory compliance, and collaboration with cross-functional teams while supporting
high-quality manufacturing operations.Key Responsibilities:
- Prepare and review validation protocols and reports for Process Validation, Cleaning Validation, Equipment Qualification, or CSV.
- Coordinate validation batches and qualification activities with Production, QA, QC, Engineering, and IT teams.
- Monitor critical process parameters and ensure adherence to approved specifications.
- Develop and execute cleaning validation sampling plans, including swab and rinse sampling.
- Support IQ, OQ, and PQ activities for equipment, systems, and utilities.
- Ensure compliance with 21 CFR Part 11, GAMP 5, and data integrity principles for GxP systems.
- Perform risk assessments, gap analysis, and maintain revalidation schedules.
- Maintain GMP-compliant documentation for audits and regulatory inspections.
Eligibility Criteria:
- Qualification: B.Pharm / M.Pharm / M.Sc. (Life Sciences / Chemistry / Microbiology)
- Experience: 2–6 years in regulated pharmaceutical / API / sterile manufacturing environments
- Exposure to GMP, ICH, WHO, USFDA, and other regulatory guidelines is essential
- Experience in Process Validation, Cleaning Validation, Equipment Qualification, or CSV
Required Skills:
- Strong understanding of validation life cycle and risk-based approach
- Good documentation and data review skills
- Ability to coordinate with cross-functional teams
- Audit readiness and familiarity with regulatory expectations
- Proficiency in MS Office and documentation systems
If you’re searching for Quality Assurance Jobs, this opportunity with Savaglobal provides an excellent platform to strengthen your pharmaceutical career. Professionals interested in Chemistry Jobs can gain valuable experience in validation, qualification, regulatory compliance, and quality systems while working in a GMP-regulated manufacturing environment. Apply today to take the next step toward a rewarding career in pharmaceutical quality assurance.
