Jr. Executive/Sr. Executive-Regulatory Affairs Jobs in SP Accure Labs Pvt Ltd - Medchal-Malkajgiri, Telangana

Jr. Executive/Sr. Executive-Regulatory Affairs Jobs in SP Accure Labs Pvt Ltd - Medchal-Malkajgiri, Telangana

work outline icon6 - 14 Years of Experiencerupess outline iconNot disclosed time outline iconFull Time

SP Accure Labs Pvt Ltd

time outline iconMedchal Malkajgiri, Telangana, India

Posted on 09-04-2026

1 Vacancy

Description

  • Job Title: Jr. Executive/Sr. Executive-Regulatory Affairs
  • Qualification: BPharm/MPharm
  • Location: SP Accure Labs Pvt Ltd - Medchal-Malkajgiri, Telangana
  • Work Experience: 6 to 14 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 SP Accure Labs Pvt Ltd - Medchal-Malkajgiri, Telangana as a Jr. Executive/Sr. Executive-Regulatory Affairs in Medchal-Malkajgiri, Telangana 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

Analytical SkillsCommunications SkillsCoordination SkillsAttention to Detail

About Organization

SP Accure Labs Pvt Ltd is a pharmaceutical organization focused on manufacturing high-quality formulations, particularly injectables and oral solid dosage forms, with a strong emphasis on regulatory compliance, product quality, and global standards. The role involves working in a manufacturing or operational environment to support production processes and ensure adherence to industry regulations. Responsibilities include assisting in production activities, following Good Manufacturing Practices (GMP), maintaining accurate batch records and documentation, monitoring equipment and process performance, and ensuring compliance with safety and hygiene protocols. The role also requires coordination with quality assurance and quality control teams, adherence to regulatory guidelines, and maintaining consistency in product quality and operational efficiency.

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