Team Member - Production

Job Summary

We are looking for a candidate to oversee manufacturing and production operations managing equipment process validation handling change controls deviations incidents and ensuring compliance with regulatory audits. Responsibilities include creating SOPs (Standard Operating Procedure) providing training and applying expertise.

Roles & Responsibilities

• You will be responsible for handling line operations specifically production and manufacturing activities like CIP (Cleaning-in-place) SIP (Sterilizing-in-place) and batch manufacturing.
• You will be responsible for handling equipment like Steam Sterilizer Dry heat sterilizer HVAC (Heating Ventilation and Air Conditioning) water system compressed air Nitrogen system etc.
• You will be responsible for process validation for Sterilization Washing Aseptic filling and cleaning procedures.
• You will evaluate change controls deviation and incident (OOS) out of specification (OOT) out of trend and risk management.
• You will prepare the production process SOPs (Standard Operating Procedures) and batch records.
• You will provide training on GMP (good manufacturing practices).
• You will apply knowledge of aseptic processes Lean OEE (Overall Equipment Effectiveness) and similar KPIs (Key Performance Indicators).
• You will respond to queries and questions regarding regulatory audits such as US FDA (Food and Drug Administration).

Qualifications :

Educational Qualification

A Bachelors or Masters degree in Pharmaceutical Sciences Chemical Engineering or a related field

Minimum Work Experience

7 years of experience in pharmaceutical manufacturing operations

Skills & Attributes Technical Skills

• Expertise in line operations especially in manufacturing activities like CIP SIP and batch manufacturing.
• Proficiency in understanding equipment such as Steam Sterilizer Dry heat sterilizer HVAC water system compressed air Nitrogen system etc.
• Understanding of Process Validation for Sterilization Washing Aseptic filling and cleaning procedures.
• Knowledge for evaluation of change control deviation incident out of specification out of trend and risk management.
• Experience in preparing production process SOPs and batch records.
• Understanding and application of Aseptic processes Lean OEE and similar KPIs.
• Hands-on experience in regulatory audits particularly with agencies like the US FDA.
• Good understanding of GMP and good laboratories practice.

Behavioural Skills

• Capacity to provide training on GMP and other relevant areas.
• Collaborates seamlessly with cross-functional teams promoting a cooperative and inclusive work environment.
• Efficiently manages time to meet production schedules and deadlines without compromising quality.
• Must have hands-on experience in sophisticated manufacturing machines and equipment.
• Effective communication and training skills for user departments and service providers.

Additional Information :

About the Department - Global Manufacturing Organisation (GMO)

At Dr. Reddys Laboratories we are dedicated to making a meaningful impact on global healthcare through precision manufacturing and innovation. With a legacy of excellence we are a leading force in the pharmaceutical industry. We operate 19 state-of-the-art manufacturing plants across Hyderabad Vizag Baddi Mexico Shreveport and Mirfield comprising 8 OSD facilities 3 Injectables facilities and 8 API facilities. Benchmarking manufacturing processes and continuous operational excellence are at the core of our capability to deliver quality medicines to our patients in 66 countries. We manufacture a portfolio of complex APIs and 1150 drug master files across key therapy areas such as Oncology Cardio-vascular Central Nervous System and Anti-Diabetes. The World Economic Forum has recognised our largest manufacturing facility in Bachupally Hyderabad as part of its Global Lighthouse Network. We aspire to be the most efficient pharma operations in the world. Our productivity improvement and digitalisation efforts are key to staying competitive meeting business imperatives and meeting our ambitious ESG goals. Building such factories of the future is integral to innovation and to build healthcare of the future.

Benefits Offered

At Dr. Reddys we actively help to catalyse your career growth and professional development through personalised learning programs. The benefits you will enjoy at Dr. Reddys are on par with the best industry standards. They include among other things and other essential equipment joining & relocation support family support (Maternity & Paternity benefits) learning and development opportunities medical coverage for yourself and your family life coverage for yourself.

Our Work Culture

Ask any employee at Dr. Reddys why they come to work every day and theyll say because Good Health Cant Wait. This is our credo as well as the guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations but as a means to help patients lead healthier lives and were always attuned to the new and the next to empower people to stay fit. And to do this we foster a culture of empathy and dynamism. People are at the core of our journey over the last few decades. They have been supported by an enabling environment that buoys individual ability while fostering teamwork and shared success. We believe that when people with diverse skills are bound together by a common purpose and value system they can make magic.

For more details please visit our career website at Work :

No

Employment Type :

Full-time