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Company Description
Lezivia Lifesciences is a well-established pharmaceutical company renowned for its commitment to providing high-quality healthcare products. Many of the company's products are manufactured at WHO-approved facilities, ensuring global standards of quality and safety. Lezivia is dedicated to delivering the best solutions for improving patient health. The company prides itself on innovation, compliance, and excellence in the pharmaceutical industry.
Role Description
This is a full-time, on-site QA-QMS role in Bahadurgarh within the pharmaceutical sector, specifically focusing on Oral Solid Dose (OSD) forms. The role involves ensuring adherence to quality standards, overseeing quality assurance (QA) processes, maintaining a robust Quality Management System (QMS), and implementing Good Manufacturing Practices (GMP). Responsibilities include conducting quality audits, managing compliance activities, and continuously improving quality processes in alignment with industry regulations and standards.
Qualifications
- Expertise in Quality Assurance and Quality Control processes, ensuring compliance with industry standards
- Strong understanding and application of Quality Management Systems (QMS) and Good Manufacturing Practice (GMP)
- Experience in conducting Quality Auditing and ensuring procedural adherence
- Attention to detail and analytical skills to identify and address quality concerns effectively
- 3-7 years of relevant experience in the pharmaceutical industry, preferably in OSD manufacturing
- Bachelor’s degree in Pharmacy, Chemistry, or a related field
- Familiarity with regulatory standards and documentation processes
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