Assistant/Deputy Manager- Production

20 hours ago

Hyderabad, Telangana, India Suraj Laboratories Full time

Company Description

Suraj Laboratories is a leading manufacturer of Generic Active Pharmaceutical Ingredients (APIs) and Pharma Intermediates, serving as a trusted Contract Manufacturing Organization (CMO) partner. The company adheres to global standards, being WHO-GMP and ISO certified, and has been successfully audited by over 65 customers across 18 months. Suraj Laboratories boasts regulatory filings including 2 US DMFs, 1 CEP, and 4 DMF-ready APIs, alongside producing multiple generic APIs and pharmaceutical intermediates. Equipped with a state-of-the-art API plant and integrated R&D facilities, the company offers expertise, precision, and quality in serving the global pharmaceutical industry from its base in India.

Key Responsibilities:

Operational & Team Leadership:

  • Lead and supervise daily production operations in assigned sections (reaction, isolation, drying, purification) for API/Intermediate manufacturing.
  • Ensure batch targets are met as per the production schedule while upholding the highest standards of Quality (cGMP), Safety, and Yield.
  • Lead, mentor, and manage a team of chemists, officers, and operators, including their training and performance development.
  • Enforce strict adherence to SOPs, safety protocols (OH&S), and environmental norms.

Planning & Deliveries:

  • Collaborate closely with the Planning and Supply Chain departments to understand the production schedule and customer commitment timelines.
  • Develop detailed weekly/daily production plans for your section to ensure seamless workflow and 
    on-time delivery
     of batches.
  • Proactively identify and mitigate potential bottlenecks in the production process that could impact deliveries.
  • Monitor inventory levels of key raw materials and intermediates in coordination with the stores department to prevent production delays.

Process & Documentation:

  • Troubleshoot operational issues, lead root cause analysis for deviations, and implement effective CAPA.
  • Drive continuous improvement projects for process optimization, yield enhancement, and cost reduction.
  • Ensure accurate and timely preparation & review of 
    Batch Manufacturing Records (BMRs)
    , logbooks, and all GMP documentation.

MIS & Management Reporting:

  • Prepare and present detailed 
    daily, weekly, and monthly MIS reports
     to the Plant Head and Senior Management.
  • Reports to include key metrics: 
    Production Output, Efficiency, Yields, Manpower Utilization, Down-time Analysis, Safety Observations, and Delivery Adherence
    .
  • Provide data-driven insights and analysis on production performance, highlighting trends, risks, and opportunities for improvement.
  • Act as a key point of contact for production data during management reviews and audits.

Qualifications & Experience:

  • Essential:
     M.Sc. (Chemistry) or B.Sc./M.Pharma/B.Pharma / B. Tech / B.E. (Chemical Engineering).
  • Experience:
     
    8-16 years
     of progressive experience in production within an 
    API/Pharma Intermediate plant working for Regulatory markets
    , with at least 3 years in a supervisory capacity.
  • Must-have:
     Proven experience in 
    production planning, meeting delivery schedules, and preparing management reports (MIS)
    .
  • In-depth knowledge of chemical processes, cGMP, and safety standards.
  • Strong analytical, problem-solving, and communication skills. Proficiency in MS Excel for data analysis is essential.

What We Offer:

  • A strategic role with direct visibility and reporting to the Plant Head.
  • The opportunity to impact both operational efficiency and business performance.
  • A culture that values safety, quality, and professional growth.

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