Quality Control Executive

Job Description

Job Title: Quality Control Executive

Company: The Livmore Lifescience Pvt. Ltd.
Location: Nanafofaliya, Vadodara, Gujarat
Experience Required: 3–4 Years
Qualification: B.Sc / M.Sc in Pharma
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 hiring a Quality Control Executive with 3–4 years of experience in a pharmaceutical API manufacturing environment. The ideal candidate should be skilled in laboratory analysis, quality testing procedures, and regulatory documentation, ensuring that all raw materials, intermediates, and finished products meet required standards.

Key Responsibilities:

• Conduct analysis of raw materials, intermediates, and finished products as per specifications
• Operate and calibrate laboratory instruments like HPLC, GC, UV, IR, etc.
• Perform stability studies and maintain associated records
• Prepare and review analytical reports, test records, and COAs
• Ensure adherence to cGMP, GLP, and safety standards in the QC laboratory
• Maintain and update SOPs and ensure proper documentation practices (GDP)
• Investigate out-of-specification (OOS) and out-of-trend (OOT) results and implement CAPAs
• Coordinate with QA, Production, and R&D for sample testing and validations
• Ensure timely completion of testing activities to support production schedules

Skills & Competencies:

• Sound knowledge of analytical techniques and instrumentation
• Strong understanding of regulatory and documentation requirements
• Good knowledge of cGMP, GLP, and ICH guidelines
• Excellent attention to detail, accuracy, and data integrity
• Ability to manage multiple tasks and meet deadlines efficiently

Benefits:

• Transportation facility from Vadodara
• Competitive salary based on experience and qualification
• Opportunity to work in a WHO-GMP compliant and quality-focused environment
• Scope for professional development and growth

To Apply:

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