Location: Verna Industrial Estate, Goa
Industry: Pharmaceutical Manufacturing – Tablets/Capsules/Formulations
Experience: 3–5 Years in QA
Qualification: B.Pharm / M.Pharm
CTC: Based on Experience and Expertise
Hands-On QA Role in Oral Solid Dosage Manufacturing
Support end-to-end Quality Assurance activities in a pharmaceutical plant with focus on compliance and validation.
Key Responsibilities
✔ In-process QA (IPQA) activities and monitoring
✔ Process and cleaning validation execution and documentation
✔ Review of Batch Production Records (BPR) & Batch Manufacturing Records (BMR)
✔ Participation in qualification and validation efforts
Mandatory Requirements
- Education: B.Pharm / M.Pharm
- Experience: 3–5 years in QA roles within a pharma formulation facility
- Skills:
- Working knowledge of validation processes and GMP documentation
- Familiar with regulatory expectations for oral solid dosage
- Attention to detail in documentation review
- Working knowledge of validation processes and GMP documentation
Why Join?
- Growth: Exposure to end-to-end QA responsibilities
- Impact: Direct contribution to product quality and compliance
- Opportunity: Advancement to QA Executive / QA Lead roles
How to Apply
Email: recruitment@avsymphonicsolutions.com
Subject: “QA Officer/Sr. Officer @ Goa – [Your Years of Exp]”
Attach: Resume with QA experience, CTC details