Drug Regulatory Affairs Executive Jobs in Theon Pharmaceuticals Ltd - Dera Bassi, Punjab
Theon Pharmaceuticals Ltd.
Dera Bassi, Punjab, India
Posted on 27-01-2026
1 Vacancy
Description
- Job Title: Drug Regulatory Affairs Executive
- Qualification: BPharm/MPharm
- Location: Theon Pharmaceuticals Ltd - Dera Bassi, Punjab
- Work Experience: 0 to 3 Years
Job Description
- Handle new drug applications, renewals, variations, and post-approval changes as per regulatory requirements.
- Ensure timely submission of drug master files (DMF), product registration applications, and license renewals.
- Maintain regulatory documents, labeling requirements, and quality-related reports.
- Ensure compliance with country-specific regulations, pharmacopoeial standards (IP, USP, BP, EP), and ICH guidelines.
- Update Standard Operating Procedures (SOPs) and regulatory checklists in alignment with the latest regulations.
- Liaise with regulatory agencies, health authorities, and certification bodies to ensure product compliance.
- Respond to regulatory queries, deficiency letters, and audits in a timely manner.
- Ensure regulatory compliance throughout the product lifecycle, including label updates, safety variations, and market expansion.
- Monitor changes in global regulatory policies and assess their impact on product registration.
Take this opportunity to join Theon Pharmaceuticals Ltd - Dera Bassi, Punjab as a Drug Regulatory Affairs Executive in Dera Bassi, Punjab and build a successful career in the healthcare industry. Apply today for this job opportunity and grow with a leading healthcare organization.
Category
Pharmaceuticals
Preferred Education
Key Skills
About Organization
Theon Pharmaceuticals Ltd, Dera Bassi, Punjab, is a reputed pharmaceutical company focused on quality-driven and compliant drug manufacturing. The company is inviting applications for Drug Regulatory Affairs Executive Jobs as part of its growing regulatory team. The role involves dossier preparation, submissions to regulatory authorities, and coordination for product approvals. It includes handling regulatory documentation, variation filings, and compliance with national and international guidelines. This opportunity offers strong regulatory exposure, professional growth, and long-term career development in a supportive environment.
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