Quality Assurance Executive

Job Description

Job Title: Quality Assurance Executive

Company: The Livmore Lifescience Pvt. Ltd.
Location: Nanafofaliya, Vadodara, Gujarat
Experience Required: 2–4 Years
Qualification: B.Sc / M.Sc / B.Pharm / M.Pharm or any relevant science background
Transportation: Company-provided transportation from Vadodara

About the Company:

The Livmore Lifescience Pvt. Ltd., established in 2016, is a WHO-GMP certified pharmaceutical company engaged in the development and manufacturing of Active Pharmaceutical Ingredients (APIs), Advanced Intermediates, and Specialty Chemicals. With a strong focus on quality, innovation, and regulatory compliance, the company aims to become the most reliable and trusted partner in the global pharmaceutical industry.

Our manufacturing facility meets WHO-GMP standards, and we are in the process of acquiring ISO 9002 certification. Our operations are aligned with regulatory requirements of FDA, EDQM, cGMP, and WHO-GMP, and supported by a state-of-the-art R&D center.

Job Description:

We are looking for a dedicated and detail-oriented Quality Assurance Executive to join our growing team. The candidate will play a key role in implementing and maintaining QA systems in compliance with cGMP and international regulatory standards.

Key Responsibilities:

• Review and ensure compliance of Batch Manufacturing Records (BMR) and Batch Packing Records (BPR)
• Support in internal audits and external regulatory audits (USFDA, WHO-GMP, etc.)
• Monitor and manage quality systems: Change Control, Deviation, CAPA, OOS, etc.
• Draft, review, and control Standard Operating Procedures (SOPs) and QA documentation
• Coordinate with Production, QC, and Warehouse for cross-functional compliance
• Conduct regular training programs on cGMP, SOPs, and quality systems
• Maintain documentation of product complaints, recalls, and market feedback
• Assist in equipment qualification, process validation, and cleanroom compliance
• Ensure accurate and timely recordkeeping as per Good Documentation Practices (GDP)

Skills & Competencies:

• Strong understanding of cGMP, ICH Q7/Q10 guidelines, and pharmaceutical QA systems
• Excellent knowledge of API manufacturing quality systems and documentation
• Analytical mindset with strong documentation and reporting skills
• Effective communication and coordination abilities
• Ability to work independently and in cross-functional teams

Benefits:

• Company-provided transportation from Vadodara
• Competitive salary based on experience and industry norms
• Opportunity to work in a WHO-GMP certified, regulatory-compliant environment
• Scope for learning, innovation, and career advancement in a dynamic pharma setting

To Apply:

📧 Email your updated resume to: jobs.dignaservices@gmail.com
📞 Contact our HR Department at: 8460441203