Drug Regulatory Affairs-Executive: Pharma OSD Full Time

Lezivia Lifesciences is a trusted pharmaceutical company known for delivering high-quality pharmaceutical products. Most of our products are manufactured at WHO-approved facilities, ensuring the highest standards of quality and safety for patients. We are committed to healthcare excellence and innovation, with a focus on providing effective and reliable solutions to meet critical health needs.

Role Description

This is a full-time on-site position for a Drug Regulatory Affairs-Executive: Pharma OSD. The role is based in the Amritsar/Ludhiana Area. The responsibilities include preparing and reviewing regulatory documentation and dossiers, ensuring compliance with regulatory requirements, and managing regulatory submissions for pharmaceutical products. The role also involves regular interaction with regulatory authorities and cross-functional teams to ensure alignment with compliance and regulatory standards.

Qualifications

• Proficiency in Regulatory Documentation and Dossier Preparation
• Knowledge of Regulatory Requirements and Compliance related to pharmaceutical products
• Experience in handling Regulatory Affairs in the pharmaceutical or healthcare industry
• Excellent organizational and communication skills
• Ability to analyze and interpret regulatory guidelines and apply them effectively
• Bachelor’s degree in Pharmacy, Life Sciences, or a related field
• Experience in oral solid dosage forms (OSD) is preferred