Executive to Sr. Executive-Regulatory Affairs Jobs in Opes Healthcare Pvt Ltd - Ahmedabad, Gujarat

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Executive to Sr. Executive-Regulatory Affairs Jobs in Opes Healthcare Pvt Ltd - Ahmedabad, Gujarat

work outline icon5 - 7 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Opes Healthcare Pvt Ltd

time outline iconAhmedabad, Gujarat, India

Posted on 24-03-2026

1 Vacancy

Description

  • Job Title: Executive to Sr. Executive-Regulatory Affairs
  • Qualification: BPharm/MPharm
  • Location: Opes Healthcare Pvt Ltd - Ahmedabad, Gujarat
  • Work Experience: 5 to 7 Years

Job Description

  • Prepare and submit regulatory dossiers for product approvals.
  • Ensure compliance with regulatory guidelines (CDSCO, WHO, USFDA, etc.).
  • Coordinate with internal teams for documentation and data collection.
  • Maintain and update regulatory files and records.
  • Handle product registrations, renewals, and variations.
  • Review labeling, packaging, and promotional materials for compliance.

Take this opportunity to join Opes Healthcare Pvt Ltd - Ahmedabad, Gujarat as a Executive to Sr. Executive-Regulatory Affairs in Ahmedabad, Gujarat and build a successful career in the healthcare industry. Apply today for this job opportunity and grow with a leading healthcare organization.

Category

Pharmaceuticals

Functional Area

Regulatory Affairs / Pharmacovigilance

Preferred Education

MPharm (Master Of Pharmacy)BPharm (Bachelor Of Pharmacy)

Key Skills

Attention to DetailAnalytical SkillsCoordination SkillsCommunications Skills

About Organization

Opes Pharmaceuticals is a pharmaceutical company engaged in the development, manufacturing, and marketing of healthcare products with a focus on quality and regulatory compliance. The company works towards meeting national and international regulatory standards for pharmaceutical products. The role involves handling regulatory affairs activities and ensuring compliance with applicable guidelines. Responsibilities include preparing and reviewing regulatory documents, coordinating submissions, and maintaining documentation. It requires working closely with internal teams and regulatory authorities. The position focuses on compliance management, documentation accuracy, and supporting product approvals in regulated markets.

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