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Team Lead – Upstream Manufacturing Biologics | Dr Reddy’s Laboratories | Hyderabad | 10.00-18.00 L


Dr. Reddys Laboratories Ltd. is an integrated global pharmaceutical company, committed to providing affordable and innovative medicines for healthier lives. Through its three businesses – Pharmaceutical Services and Active Ingredients, Global Generics and Proprietary Products Dr. Reddys offer a portfolio of products and services including APIs, custom pharmaceutical services, generics, biosimilars, and differentiated formulations.

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   The major therapeutic focus is on gastrointestinal, cardiovascular, diabetology, oncology, pain management, and anti-infective. Major markets include India, USA, Russia-CIS, and Europe apart from other select geographies within Emerging Markets. For more information, log on to www.drreddys.com

Position: Team Lead Upstream Manufacturing – Biologis

Location: Bachupally, Hyderabad, Telangana, India

Team Size: 10-12 FTEs and close to 20 contract employees

Job Description:

Purpose of Job:

  • To Lead the downstream/ Upstream manufacturing team and oversee the implementation of production schedules.
  • With the objective of producing products in defined terms of volumes and timelines, while ensuring compliance to quality standards, GMP, and other regulatory and statutory requirements, as per schedule.

Areas of Responsibility:


  • Receive the inputs from production planning and plan the daily operation on the production floor, including scheduling, staffing, monitoring, training, and troubleshooting
  • To ensure that all operations are in full compliance with applicable BPRs / EBRs, SOPs, and safety guidelines;
  • Responsible for understanding and administration contract manpower

Compliance & Documentation

  • Issue discrepancies and work with cross-functional departments to close the discrepancies and implement appropriate corrective actions;
  • Comply with all relevant GMP, safety standards, and SOPs of the operation of designated manufacturing equipment.
  • Complete batch documentation in compliance with GMP.
  • Collection and maintenance of data in accordance with cGMPs, company standards, policies, and other regulatory requirements;

Equipment validation

  • Maintaining manufacturing equipment to ensure correct functionality and calibration compliance.
  • Operation of manufacturing equipment and automated systems within the validated process parameters

Safety & Facility Inspection

  • Actively promote safety awareness and improvements.
  • Proactively engage in continuous improvement activities.
  • Adhere to the company safety rules and conduct all work in a manner to report all unsafe matters and near-miss /accidents.

Team Management

  • Goal setting/performance reviews
  • Training and coaching employees;
  • Effectively managing employee performance issues and corrective actions
  • Recognizing and appreciating employee contributions, and all other activities/functions which support the achievement of individual/department/business objectives

Business Understanding

  • Understanding of process manufacturing, Quality Systems, and regulatory environment

Qualification: B.Tech/B.E Chemical/B.Sc

Experience: 6 Years in Biosimilars

Salary: 10,00,000 TO 18,00,000 INR CTC/PA

Contact Details:

Mr. Naresh Kumar – Talent Acquisition

nareshkumar.g@drreddys.com, talent@drreddys.com

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