Regulatory Affairs Manager Jobs in Sydler Remedies Pvt Ltd - Mumbai, Maharashtra

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Regulatory Affairs Manager Jobs in Sydler Remedies Pvt Ltd - Mumbai, Maharashtra

work outline icon9 - 14 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

Sydler Remedies Pvt Ltd

time outline iconMumbai, Maharashtra, India

Posted on 01-05-2026

1 Vacancy

Description

  • Job Title: Regulatory Affairs Manager
  • Location: Sydler Remedies Pvt Ltd - Mumbai, Maharashtra
  • Work Experience: 9 to 14 Years
  • Qualification: M.Pharma

Job Description

  • Manage regulatory submissions for domestic and export markets.
  • Prepare and review dossiers (CTD, eCTD, ACTD).
  • Ensure compliance with regulatory guidelines (CDSCO, USFDA, EMA).
  • Coordinate with QA, QC, and R&D for documentation.
  • Handle queries, deficiencies, and regulatory correspondence.
  • Manage product registrations, renewals, and variations.
  • Track regulatory changes and implement updates.
  • Support audits and inspections from regulatory authorities.

Take this opportunity to join Sydler Remedies Pvt Ltd - Mumbai, Maharashtra as a Regulatory Affairs Manager in Mumbai, Maharashtra 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)

Key Skills

Good Communication SkillsTeam working SkillsAttention to DetailDecision-Making Skills

About Organization

Sydler Remedies Pvt. Ltd. is a pharmaceutical organization engaged in the manufacturing of high-quality formulations, nutraceuticals, herbal, and cosmeceutical products with a strong focus on regulatory compliance, product quality, and global standards. The role involves working in a manufacturing or operational environment to support production processes and ensure compliance with industry standards. Responsibilities include assisting in production activities, monitoring process parameters, maintaining accurate batch records and documentation, and ensuring adherence to safety, hygiene, and environmental guidelines. The role also requires coordination with quality assurance and quality control teams, following Good Manufacturing Practices (GMP), and contributing to consistent product quality and efficient operations.

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