BDR Pharmaceutical Regulatory Affairs Fresher and Experienced

BDR Pharmaceutical Regulatory Affairs Jobs for Fresher and Experience | Apply Now

BDR Pharmaceuticals, a leader in pharmaceutical formulation, is expanding its Regulatory Affairs (RA) team and is offering exciting career opportunities for freshers and experienced professionals alike. If you hold a M.Pharm or B.Pharm degree and have a passion for regulatory compliance and pharmaceutical innovation, this is the perfect opportunity to join one of the most dynamic companies in the industry. Positions are available across US, EU, Health Canada, Australia, and Brazil markets at our Baska, Halol location.

Job Openings at BDR Pharmaceuticals

BDR Pharmaceuticals is currently hiring for various Regulatory Affairs (RA) roles, catering to both freshers and professionals with experience in CMC (Chemistry, Manufacturing, and Controls). Below is a breakdown of the positions available:

1. Officer / Senior Officer – Regulatory Affairs

• Experience: 0-3 years in RA (Preferably in US/EU Markets)
• Qualification: M.Pharm / B.Pharm
• Job Responsibilities:
  • Preparation, review, and submission of regulatory dossiers in compliance with market requirements for the US, EU, Brazil, and Canada.
  • Manage CMC documentation for pharmaceutical products.
  • Collaborate with cross-functional teams to ensure timely dossier submission.

This position is ideal for freshers looking to kickstart their career in regulatory affairs. You’ll gain hands-on experience in preparing and managing regulatory submissions across global markets.

2. Executive / Senior Executive – Regulatory Affairs

• Experience: 3-5 years in RA (Preferably in US/EU Markets)
• Qualification: M.Pharm / B.Pharm
• Job Responsibilities:
  • Lead the preparation of high-quality regulatory submissions.
  • Compile and manage complex CMC documentation for solid and injectable dosage forms.
  • Ensure compliance with global regulatory requirements for US, EU, Health Canada, and Brazil markets.

This role is suited for professionals with a few years of experience, looking to take on more responsibility in regulatory submissions for various dosage forms.

3. Assistant Manager / Deputy Manager – Regulatory Affairs

• Experience: 5-8 years in RA (Preferably in US/EU Markets)
• Qualification: M.Pharm / B.Pharm
• Location: Baska, Halol
• Job Responsibilities:
  • Develop and execute regulatory strategy for complex injectables and ophthalmic products.
  • Lead dossier review and ensure regulatory compliance for global submissions.
  • Collaborate with internal and external stakeholders to streamline regulatory processes.

How to Apply for BDR Pharmaceutical Regulatory Affairs Roles

Are you passionate about regulatory compliance and pharmaceutical innovation? If so, BDR Pharmaceuticals invites you to apply for any of the roles listed above. Simply send your resume to hrd@bdrpharma.com or contact us via 8328847433 to schedule your interview.