Venus Remedies Hiring Production (Oncology) and Drug Regulatory Affairs

Are you a qualified B.Pharma or M.Pharma professional seeking exciting career growth opportunities? Venus Remedies Ltd., a global leader in pharmaceuticals, is currently hiring for its Production (Oncology) and Drug Regulatory Affairs departments. With a focus on innovation and quality, Venus Remedies provides an exceptional work environment and opportunities for career advancement. Join us in contributing to life-saving oncology solutions and driving regulatory success in a highly competitive market.

Available Job Positions at Venus Remedies

Venus Remedies is offering two key roles across its Injectable Plant and Regulatory Affairs departments:

1. Production (Oncology)

• Department: Production (Oncology)
• Section: Manufacturing/Filling/Autoclave
• Experience: 3 to 6 years
• Designation: Sr. Executive/Executive
• Qualifications: B.Pharma
• Location: Baddi
• Job Description: The ideal candidate will have hands-on experience in injectable production, including working in manufacturing, filling, and autoclaving processes. Knowledge of GMP (Good Manufacturing Practices) is essential for this role. Candidates will be responsible for ensuring efficient production operations and meeting the stringent standards required in oncology pharmaceuticals.
• Key Responsibilities:
  • Overseeing the manufacturing process of oncology injectables.
  • Ensuring compliance with safety and regulatory guidelines.
  • Managing autoclave operations to ensure sterilization and quality control.

2. Drug Regulatory Affairs

• Department: Drug Regulatory Affairs
• Experience: 3 to 10 years
• Designation: Manager/Executive
• Qualifications: M.Pharma/B.Pharma
• Location: Panchkula
• Job Description: The Regulatory Affairs professional will manage submissions, regulatory filings, and compliance with various regulatory authorities globally. A deep understanding of global regulatory standards and experience in the Regulatory Market is crucial.
• Key Responsibilities:
  • Preparing and submitting drug dossiers to regulatory authorities.
  • Ensuring compliance with the latest regulatory standards and guidelines.
  • Coordinating with internal teams to maintain high-quality submissions.

How to Apply

Send your resume to hra_staff5@venusremedies.com or contact via WhatsApp at 9882859675