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Company Description Lezivia Lifesciences is a respected pharmaceutical company recognized for delivering high-quality products to patients. Most of its formulations are manufactured at WHO-approved facilities, reflecting a strong commitment to global quality and safety standards. The organization focuses on consistent product performance, regulatory compliance, and patient well-being. Professionals joining Lezivia Lifesciences can expect a quality-driven environment with robust manufacturing processes and clear standards. The company values integrity, reliability, and adherence to international best practices in pharma manufacturing.
Role Description This is a full-time, on-site role based at Lezivia Lifesciences’ Pharma OSD (Oral Solid Dosage) plant in Roorkee, offering opportunities for QC Analysts (5+ years of experience) and QC Reviewers (9–10 years of experience). QC Analysts will perform routine and non-routine testing of raw materials, in-process samples, and finished products, operate and maintain laboratory equipment, document results, and support investigations related to out-of-specification or deviations. QC Reviewers will review and verify analytical data, test reports, and batch records for accuracy and compliance, oversee adherence to quality control and quality assurance procedures, and provide guidance to the QC team on regulatory and internal standards. Both roles collaborate closely with production, QA, and regulatory teams to ensure products meet established specifications and GMP requirements. The positions involve strict adherence to safety protocols, timely completion of testing and reviews, and continuous improvement of laboratory practices.
Qualifications
- Candidates should possess strong Analytical Skills for interpreting test results, identifying trends, and supporting investigations.
- Candidates should possess Quality Control expertise, including routine testing, documentation, and compliance with GMP and regulatory guidelines.
- Candidates should possess solid Laboratory Skills, including sample handling, method execution, and adherence to lab safety procedures.
- Candidates should possess proficiency in operating and maintaining Laboratory Equipment relevant to OSD testing (e.g., HPLC, UV, dissolution apparatus, balances).
- Candidates should possess Quality Assurance understanding to ensure data integrity, support audits, and maintain documentation standards.
- Relevant bachelor’s or master’s degree in Pharmacy, Chemistry, or a related scientific discipline.
- Prior experience in a pharmaceutical OSD plant or similar regulated environment, with familiarity in WHO-GMP and other regulatory requirements.
- Strong attention to detail, effective communication skills, and the ability to work collaboratively within cross-functional teams.
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