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Company Description
Lezivia Lifesciences is a highly reputed pharmaceutical company recognized for delivering high-quality products. Our offerings are manufactured in WHO-approved facilities, ensuring products meet stringent international quality standards. We are dedicated to providing effective and reliable solutions to improve patient health. At Lezivia, we prioritize excellence and innovation in every product we create.
Role Description
This is a full-time on-site position for a QA Professional specializing in Oral Solid Dosage at Lezivia Lifesciences. The role is based in the Amritsar/Ludhiana area. Responsibilities include overseeing quality control processes, ensuring adherence to Good Manufacturing Practices (GMP), conducting quality audits, and maintaining quality management systems. The QA Professional will play a critical role in ensuring compliance with industry regulations and delivering high-quality pharmaceutical products.
Qualifications
- Proficiency in Quality Control and Quality Assurance processes.
- Strong knowledge of Good Manufacturing Practices (GMP) and Quality Management principles.
- Experience with Quality Auditing and maintaining adherence to regulatory standards.
- Strong analytical, problem-solving, and attention-to-detail skills.
- Bachelor's or Master's degree in Pharmacy, Chemistry, or a related field.
- Prior experience in the pharmaceutical industry, particularly with oral solid dosage forms, is highly desirable.
- Excellent organizational and communication skills, with the ability to work both independently and as part of a team.
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