Drug Regulatory Affairs Manager Jobs in Sahaj Pharma - Kandivali, Mumbai

Drug Regulatory Affairs Manager Jobs in Sahaj Pharma - Kandivali, Mumbai

work outline icon10 - 12 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Sahaj Pharma

time outline iconMumbai, Maharashtra, India

Posted on 27-01-2026

1 Vacancy

Description

  1. Job Title: Executive/Sr. Executive -Operations
  2. Qualification: MPharm
  3. Location: Sahaj Pharma - Kandivali, Mumbai
  4. Work Experience: 10 to 12 Years

Job Description

  1. Prepare, review, and submit regulatory dossiers for product registrations.
  2. Liaise with regulatory authorities (CDSCO, DCGI, USFDA, EMA, etc.).
  3. Monitor and implement regulatory changes to ensure compliance.
  4. Manage post-approval changes, renewals, and variations for products.
  5. Ensure labeling, packaging, and promotional material compliance.
  6. Respond to regulatory queries and deficiency letters in a timely manner.
  7. Support regulatory inspections and audits.
  8. Maintain regulatory databases and documentation systems.
  9. Provide regulatory guidance to internal teams for new projects.
  10. Develop and implement regulatory strategies for domestic and international markets.
  11. Ensure timely submission of compliance reports and other regulatory filings.

Take this opportunity to join Sahaj Pharma - Kandivali, Mumbai as a Executive/Sr. Executive -Operations in Kandivali, Mumbai 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

MPharm (Master Of Pharmacy)

Key Skills

Communication SkillsDocumentationMarketingTeam Coordination

About Organization

Sahaj Pharma, Kandivali, Mumbai, is a reputed pharmaceutical company focused on quality-driven and compliant drug manufacturing. The company is inviting applications for Drug Regulatory Affairs Manager Jobs as part of its growing regulatory team. The role involves managing dossiers, regulatory submissions, and coordination with authorities for product approvals. It includes overseeing regulatory documentation, variation filings, and ensuring compliance with national and international guidelines. This opportunity offers strong leadership exposure, professional growth, and long-term career development in a supportive environment.

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