Regulatory Affairs

1 day ago

Mumbai, Maharashtra, India Olive PharmaScience Ltd Full time

Company Description

Olive PharmaScience Ltd has been a leader in global healthcare innovation for over five decades, providing high-quality pharmaceutical solutions, including customized pharmaceuticals, OTC products, and dietary supplements. The company specializes in advanced soft gelatine dosage forms, using state-of-the-art research and manufacturing facilities in India that meet the highest cGMP standards. Olive PharmaScience Ltd is committed to improving therapeutic effectiveness and setting benchmarks in patient care through innovative formulations. With a focus on precision, quality, and global partnerships, the company continues to transform traditional oral dosage forms into advanced solutions for healthcare needs worldwide.

Role Description

This is a full-time, on-site role for a Regulatory Affairs - Executive/Senior Executive at our Corporate Office in Mumbai. The ideal candidate will be responsible for preparing and reviewing regulatory submissions, ensuring compliance with local and international regulatory requirements, and supporting dossier compilation for product registrations. Coordination with internal teams and regulatory authorities to address compliance matters and document submissions will also be key responsibilities.

Qualifications

  • Strong knowledge of Regulatory Documentation, Dossier Preparation, and Regulatory Affairs practices
  • Familiarity with Regulatory Requirements and Regulatory Compliance standards
  • Familiarity with Formulation Dossier Preparations
  • Attention to detail and ability to maintain accurate records
  • Excellent communication and documentation skills
  • Bachelor's or Master's degree in Pharmacy, Pharmaceutical Sciences, or a related field
  • Experience in the pharmaceutical industry, particularly in regulatory roles, is preferred
  • Ability to work collaboratively with cross-functional teams

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