DRA Specialists : Pharmaceutical OSD Experienced| Salary up to ₹60,000 PM

Company Description Jaidev Pharma Placement is India’s leading hiring partner for the pharmaceutical and healthcare industry, specializing in building high-performing teams that drive growth and long-term impact. In just five years, the firm has partnered with over 75 organizations across India, supported by a strong network of more than 350,000 pharma professionals. Backed by over 20 years of pharma industry experience and dedicated recruitment expertise, Jaidev Pharma Placement focuses on matching talent with business needs and market dynamics. With offices in Gurgaon, the Mumbai region, and Hyderabad, and a passionate multidisciplinary team, the company delivers strategic hiring solutions, training support, and performance enhancement programs.
Role Description The DRA Specialist: Pharmaceutical OSD Experienced role is a full-time, on-site position based in New Delhi. The specialist will prepare, review, and submit regulatory dossiers for oral solid dosage (OSD) pharmaceutical products in accordance with national and international guidelines. Daily responsibilities include coordinating with QA, QC, production, R&D, and RA teams to gather documentation, ensure compliance with GMP, and maintain accurate regulatory records. The role involves responding to regulatory queries, tracking approvals, updating internal databases, and supporting product lifecycle management from registration through post-approval variations. The specialist will also monitor changes in regulatory requirements, support audits, and contribute to continuous improvement in documentation and compliance processes.
Qualifications

• Candidates should possess strong knowledge of Pharmacy and Pharmaceuticals, particularly in oral solid dosage forms.
• Candidates should possess a solid understanding of Good Manufacturing Practice (GMP) and regulatory compliance standards.
• Candidates should possess relevant Laboratory Skills for handling documentation related to quality control, stability studies, and analytical methods.
• Candidates should possess basic Sales and commercial awareness to align regulatory strategies with market and business needs.
• Bachelor’s or Master’s degree in Pharmacy or a related pharmaceutical discipline.
• Prior experience in DRA for OSD products in a regulated pharmaceutical environment.
• Strong attention to detail, documentation accuracy, and ability to meet deadlines.
• Proficient in MS Office and regulatory documentation tools; good written and verbal communication skills.
• Ability to collaborate effectively with cross-functional teams and adapt to evolving regulatory guidelines.