Executive QA at SAVA Healthcare – Validation & Qualification, Apply Now!
Are you a QA professional with hands-on experience in validation and qualification processes? SAVA Healthcare Limited is hiring for the role of Executive / Senior Executive – QA (Validation & Qualification) at its Indore Plant. This opportunity is ideal for individuals eager to contribute to a high-performing Quality Assurance team in a regulated pharmaceutical manufacturing setup.
- Job Title: Executive / Senior Executive – QA (Validation & Qualification)
- Location: Indore Plant
- Department: Quality Assurance (QA)
- Industry: Pharmaceutical/Manufacturing
- Reports to: QA Manager – Validation / Head QA
About The Company
SAVA Healthcare Limited is committed to delivering world-class pharmaceutical solutions backed by science, safety, and compliance. Join us to make a meaningful impact in the healthcare space while advancing your career in quality assurance.
Executive QA at SAVA Healthcare Role Summary
The role involves supporting Validation & Qualification activities in areas such as Process Validation, Cleaning Validation, Facility & Equipment Qualification, and Computer System Validation (CSV).
Key Responsibilities
Process Validation
- Prepare and review Process Validation Protocols and Reports (PV).
- Coordinate validation batches with cross-functional teams.
- Monitor critical process parameters and ensure adherence to approved specifications.
- Perform risk assessments and gap analysis as required.
Cleaning Validation
- Develop and execute cleaning validation protocols and sampling plans.
- Perform visual inspection and swab/rinse sampling for various equipment.
- Review analytical data and calculate MACO/Residue Limits.
- Maintain cleaning validation matrix and revalidation schedules.
Facility & Equipment Qualification
- Support IQ, OQ, PQ of equipment, systems, and utilities as per validation master plan.
- Participate in installation, commissioning, and qualification activities.
- Ensure periodic qualification and requalification as per schedule.
- Maintain GMP-compliant records and reports for audits and inspections.
Computer System Validation (CSV)
- Prepare and review URS, RA, IQ/OQ/PQ protocols for GxP systems.
- Ensure compliance with 21 CFR Part 11, GAMP 5, and data integrity principles.
- Coordinate with IT, QA, and software vendors during validation life cycle.
- Maintain validation documentation and change control records.
Executive QA at SAVA Healthcare Candidate Profile
- Qualification: B.Pharm / M.Pharm / M.Sc. (Life Sciences / Chemistry / Microbiology)
- Experience: 2–6 years in regulated pharmaceutical / API / sterile manufacturing environments
Desired Skills
- Strong understanding of validation life cycle and risk-based approach.
- Good documentation and data review skills.
- Ability to coordinate with cross-functional teams (Production, QA, QC, Engineering, IT).
- Audit readiness and familiarity with regulatory expectations.
- Proficiency in MS Office and documentation systems.
Employment Type: Full-Time
CTC: As per industry norms and candidate’s experience
Keywords: QA job, Validation, Qualification, Quality Assurance, Pharmaceutical Manufacturing, Indore, GMP, B.Pharm, M.Pharm, M.Sc., Process Validation, Cleaning Validation, Equipment Qualification, CSV
