QA Validation

5 days ago

Karachi South District, Sindh, Pakistan W. Woodward Pakistan Pvt. Ltd. Full time 900,000 - 1,200,000 per year

Company Description

Le-Mendoza Pharmaceutical Pvt. Ltd., established in 1971, is a reputed national pharmaceutical company specializing in the manufacturing and distribution of high-quality medicines across the country. The organization produces a broad range of products, including antibiotics, tablets, capsules, syrups, suspensions, oral electrolyte solutions, dry powder suspensions, and injectables. Committed to excellence, Le-Mendoza strives to exceed customer expectations and achieve world-class quality standards. With a dedication to continuous improvement and a customer-centric approach, the company aims to be the first choice for both customers and employees.

Role Description

QA Validation Dept: This is a full-time, on-site role for our location at Metrovil SITE & Korangi for a Pharmacist specializing in Quality Assurance (QA) and Validation, located in Karachi South District. The role includes monitoring quality assurance activities, executing validation protocols, ensuring compliance with regulatory standards, according to cGMP and supporting the development and implementation of quality control processes. Day-to-day tasks involve evaluating documentation, conducting inspections, testing procedures, and identifying areas for improvement within production and validation cycles.

Production Pharmacist: Operate batch execution for granulation, compression, and coating per BMR & SOPs. Operate & supervise RMG, FBD, Tablet Press, Auto Coater, and Compression Machines.

Ensure line clearance, in-process checks, and real-time documentation.

Maintain cGMP / GDP compliance and regulatory standards.

Promote safety, housekeeping, and support validation (IQ/OQ/PQ) activities.

Qualification: B.Pharm / M.Pharm / B.Sc / M.Sc

Qualifications

· Strong expertise in Quality Assurance and Validation processes, including experience in creating and executing validation protocols.

· Knowledge of regulatory compliance and quality control standards according to cGMP within the pharmaceutical industry.

· Attention to detail, excellent analytical skills, and the ability to identify and address process improvement areas.

· Effective communication and documentation skills for reporting and collaboration with cross-functional teams.

·       Minimum Bachelor's degree in Pharmacy or a related field; advanced certifications or degrees are a plus.

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