Block Incharge

1 day ago


Hyderabad, Telangana, India Aurore Life Sciences Full time ₹ 15,00,000 - ₹ 25,00,000 per year

Job Title: API Production Block In-Charge

Department: Manufacturing / Production

Location: [Insert Location]

Reports To: Production Manager / Plant Head

Qualification: B.Sc / M.Sc in Chemistry, B.Tech / M.Tech in Chemical Engineering or related field.

Job Purpose:

To oversee and manage day-to-day operations of the API production block, ensuring efficient, safe, and compliant manufacturing of Active Pharmaceutical Ingredients in accordance with cGMP and regulatory requirements.

Key Responsibilities:

Production Management:

  • Plan, coordinate, and execute API production schedules to meet manufacturing targets.
  • Monitor daily production activities, troubleshoot process issues, and ensure minimal downtime.
  • Ensure proper batch documentation as per cGMP and SOPs.
  • Coordinate with QA/QC, Engineering, EHS, and other departments to ensure smooth production flow.

Compliance and Documentation:

  • Ensure strict adherence to GMP, regulatory, and safety guidelines.
  • Review and approve batch manufacturing records (BMR), logbooks, and other documentation.
  • Participate in internal and external audits (USFDA, EU, WHO, etc.) and implement corrective actions.

Team Management:

  • Lead and supervise production operators, shift chemists, and technical staff.
  • Provide training on SOPs, safety practices, and equipment handling.
  • Maintain discipline and productivity within the team.

Process Improvement:

  • Identify process inefficiencies and work with R&D or process teams to optimize yields, reduce waste, and improve productivity.
  • Support technology transfer and scale-up activities from R&D to commercial scale.

Equipment & Facility Oversight:

  • Ensure all equipment is calibrated, qualified, and maintained.
  • Coordinate with maintenance for timely servicing and breakdown response.

Skills & Competencies:

  • Strong understanding of chemical processes in API manufacturing.
  • Sound knowledge of cGMP, ICH, and regulatory requirements.
  • Leadership and team management abilities.
  • Analytical thinking and problem-solving.
  • Excellent communication and coordination skills.

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