Position: Manager Production

Department: Production/Manufacturing Operations

Reporting to: Production Head

Experience: 12-15 Years

Location: Hyderabad

Role Overview The Manager – Production role presents an exciting opportunity to lead pharmaceutical manufacturing operations in a cGMP-regulated workplace.

Responsibilities include overseeing day-to-day production across granulation, compression, coating, and packing, driving process validation and technology transfer, ensuring regulatory inspection readiness, and building high-performing shop-floor teams. The ideal candidate brings 12 to 15 years of production leadership experience, a strong compliance-first mindset, proven greenfield project exposure, and the ability to collaborate effectively with Quality, Engineering, and Supply Chain teams. Join us to make a significant impact in the dynamic field of pharmaceutical manufacturing.

A Challenging Task

- Lead and manage day-to-day production operations across granulation, compression, coating, and packing sections, ensuring targets are met as per the production plan.
- Supervise and develop a large production team, driving performance, training, and accountability across shifts.
- Ensure strict adherence to cGMP guidelines, safety standards, and regulatory requirements across all manufacturing activities.
- Prepare and review SOPs, BMRs (Batch Manufacturing Records), and other production documentation.
- Drive process validation activities including IQ/OQ/PQ and support technology transfer and scale-up of new products.
- Monitor and improve manufacturing KPIs such as yield, cycle time, OEE, and lead-time reduction through Lean/Kaizen initiatives.
- Support equipment commissioning, FAT/SAT activities, and greenfield project execution as required.
- Ensure audit readiness and actively participate in regulatory inspections (US FDA, MHRA, WHO, TGA, ANVISA, CDSCO, etc.), addressing observations with corrective and preventive actions.
- Handle change control, deviation management, and risk assessments (FMEA) related to production processes.
- Coordinate cross-functionally with Quality, Engineering, Warehouse, and Supply Chain teams to ensure smooth production flow.
- Plan manpower, machine, and material requirements to meet production schedules efficiently.
- Drive digital manufacturing initiatives (MES, DAS, recipe management) for process efficiency and data integrity.
- Report production performance, issues, and improvement plans to senior management/Site Head.
- Monitor raw material and consumable stock levels in coordination with warehouse/stores to avoid production delays.




- Ensure timely calibration and preventive maintenance of production equipment in coordination with the Engineering team.
- Review and approve batch documentation, ensuring data integrity and compliance with regulatory standards (ALCOA+ principles).
- Drive root cause analysis (RCA) and CAPA implementation for production-related deviations and non-conformances.
- Plan and conduct periodic training programs for shop-floor staff on GMP, safety, and process updates.
- Support new product introduction (NPI) and formulation transfer activities from R&D; to commercial production.
- Optimize batch cycle times and reduce changeover time through process improvement initiatives.
- Ensure proper implementation of 5S, housekeeping, and safety standards across the production floor.
- Prepare monthly/quarterly production reports, budgets, and cost-control initiatives in line with organizational goals.
- Liaise with QA and QC departments to ensure timely batch release and resolve quality-related bottlenecks.

Who We Are Looking For
- A results-driven, hands-on manufacturing professional with established shop-floor credibility and a strong compliance-first approach. Preferred candidates will have extensive experience in High Potent OSD or General OSD operations, with comprehensive knowledge of GMP, quality systems, EHS standards, and regulatory expectations.
- The role requires a leader who can seamlessly balance production targets with uncompromising compliance standards, proactively resolve operational challenges, drive process optimization, and inspire teams to achieve sustained improvements in productivity, quality, and cost efficiency.
- An individual who enjoys working at the interface between production operations and cross-functional teams.
- A proactive team player with strong organizational, planning, and communication skills.
- Someone who can manage multiple priorities while maintaining a high level of accuracy and regulatory compliance.
- A professional who is eager to drive continuous improvement and contribute ideas for process optimization.

A Convincing Background
- M.Pharmacy / B.Pharmacy or any relevant qualification in Life Sciences, Pharmacy, or a related discipline.
- 12 to 15 years of experience in Pharmaceutical Manufacturing (cGMP regulated setting).
- Proven track record in greenfield facility setup, commissioning,



and commercial production scale-up.
- Experience with process validation (IQ/OQ/PQ), technology transfer, and SOP/BMR development.
- Exposure to regulatory inspections by US FDA, MHRA, WHO, TGA, ANVISA, CDSCO, or similar authorities.
- Strong understanding of change control, deviation management, and risk assessment (FMEA).
- Proficiency in MS Office and manufacturing systems (SAP, MES, DAS) along with strong communication skills.

Which mindset will you meet at Tiefenbacher
- We strive towards developing curious team members from all over the world who love to challenge the status quo, take on responsibility, enjoy collaborating and have an affinity and passion for health care. At all Tiefenbacher Group companies, you will meet a fast-paced work environment where everybody is welcome to suggest new ideas and take ownership of their realization. On a daily basis, we are working towards a culture characterized by curiosity, high energy levels and openness to mutual feedback. We also value a good sense of humor and optimism, especially during hectic times.

Our Leadership Philosophy
- We are open to prospective team member hoping to gain initial leadership experience. We highly value people skills and empathy. It is particularly important to us that you support employees in their personal and professional development. An open communication style and a balance between promoting team performance and individual development are key aspects of this role. We are looking for a leader who likes to embrace and support new approaches and initiatives and is willing to take thoughtful risks. A strong interest in your own development is also desirable. You will receive support in developing your leadership skills from the reporting manager as well as the entire leadership team and management of the company. This support will give you the opportunity to continuously grow and develop within a dynamic leadership team.

Why join us
- Joining Tiefenbacher Laboratories means becoming part of a global mission to make high-quality, affordable medicines accessible to all. At our Hyderabad facility, you will work alongside passionate professionals in a cooperative, innovation driven environment where your ideas and contributions truly matter. We offer structured career development, international exposure, and a culture that values integrity, diversity, and scientific excellence.
- Our commitment to sustainability, ethical practices, and employee well-being ensures a workplace that’s not only rewarding but also meaningful. Be part of a team that’s shaping the future of healthcare locally and globally.

📌 Manager - Production (Hyderabad)
🏢 Tiefenbacher Laboratories
📍 Hyderabad