CiRO Pharma Private Limited is conducting a walk-in interview for multiple positions in Regulatory Affairs, Production (Softgel), and FRD (Formulation Research & Development) at its facility in Siddipet, Telangana.

Walk-In Details

1. Regulatory Affairs – Formulations

Senior Executive – US

Key Responsibilities

• Regulatory strategy and lifecycle management.
• Dossier preparation and compliance.
• Electronic submission management.
• Coordination with regulatory authorities and internal teams.

Senior Executive – EMA

Key Responsibilities

• Regulatory strategy for European markets.
• Dossier compilation and submission.
• Lifecycle management activities.
• Electronic submission management.

Senior Executive – EM/ROW

Key Responsibilities

• Regulatory affairs for Emerging Markets and Rest of World (ROW).
• Product registration and lifecycle management.
• Dossier preparation and compliance activities.
• Electronic submissions and regulatory coordination.

2. Production – Softgel

Bottle Line Operator

Key Responsibilities

• Bottle line operations in Soft Gelatin manufacturing.
• Line setup, changeovers, and equipment handling.
• In-process quality checks and GMP compliance.
• Equipment troubleshooting and routine monitoring.
• Production documentation and batch record maintenance.
• Safety, hygiene, and SOP compliance.

3. FRD (Formulation Research & Development)

Executive

Key Responsibilities

• Formulation development and optimization using QbD principles.
• Execution of formulation trials and documentation in laboratory notebooks.
• Preparation and review of development, validation, stability, and manufacturing documents.
• Technology transfer support from laboratory scale to commercial production.
• Compliance with regulatory requirements and industry standards.

Operator – FRD

Key Responsibilities

• Operation of R&D and pilot-scale pharmaceutical equipment.
• Handling:
  • Compression Machines
  • Coating Machines
  • Packaging Equipment
  • Formulation Development Process Equipment
• Supporting formulation development and scale-up activities.

Total Openings

Preferred Candidate Profile

Regulatory Affairs

• Experience in formulation dossier preparation.
• Knowledge of USFDA, EMA, and Emerging Market regulations.
• Hands-on experience with eCTD and electronic submissions.

Production – Softgel

• Experience in softgel manufacturing operations.
• Strong GMP and batch documentation knowledge.
• Exposure to bottle line operations and troubleshooting.

FRD

• Experience in formulation development and optimization.
• Knowledge of QbD principles and technology transfer.
• Familiarity with pilot-scale and R&D equipment.

Documents to Carry

• Updated Resume
• Educational Certificates
• Experience Certificates
• Latest Salary Slips
• Government ID Proof
• Passport-Size Photographs

Why Join CiRO Pharma?

• Opportunities across Regulatory Affairs, Production, and R&D.
• Exposure to global regulatory markets (US, EMA, ROW).
• Career growth in formulation development and softgel manufacturing.
• Work in a growing pharmaceutical organization with multiple specialized functions.

Eligible candidates can attend the walk-in interview on 20th June 2026 from 10:00 AM onwards at CiRO Pharma Private Limited, Siddipet, Telangana.

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