Location: Nelamangala Industrial Area, Bengaluru
Industry: Sterile Pharmaceutical Manufacturing
Experience: 3–5 Years in Sterile QA Validation
Qualification: B.Pharm / M.Pharm / B.Sc. / M.Sc.
CTC: ₹4–5.5 LPA (Based on Experience)
Opportunity for Early-Career Validation Professionals
Join our USFDA/EU-GMP sterile injectable facility as a QA Validation Executive to grow your expertise in critical compliance processes.
Key Responsibilities
✔ Assist in executing validation protocols (Equipment, HVAC, Autoclave, CIP/SIP).
✔ Support review of cleaning validation, smoke studies, and environmental monitoring.
✔ Maintain documentation as per cGMP and internal quality systems.
✔ Work with cross-functional teams during IQ/OQ/PQ activities.
✔ Handle minor deviations/CAPAs under supervision.
Mandatory Requirements
Education: B.Pharm / M.Pharm / B.Sc. / M.Sc. (Microbiology/Chemistry preferred).
Experience:
- 3+ years in sterile pharma validation (injectables preferred).
- Exposure to autoclave/HVAC validation in Grade A/B areas.
Skills: - Basic knowledge of GMP/GLP, 21 CFR Part 11.
- Familiarity with QMS software (TrackWise, LIMS).
- Strong documentation and teamwork skills.
Why Join?
Skill Development: Train under validation experts.
Regulatory Exposure: Learn USFDA/EU-GMP compliance.
Growth Path: Progress to Senior Executive in 2–3 years.
How to Apply
Email: recruitment@avsymphonicsolutions.com
Subject: “QA Validation Executive @ Bengaluru – [Your Years of Exp]”
Attach: Resume, Current CTC, Expected CTC, Notice Period.