Job Description

Company DescriptionDr. Reddy\xe2\x80\x99s Laboratories Ltd. is a leading multinational pharmaceutical company based across global locations. Each of our 24,000 plus employees comes to work every day for one collective purpose: to accelerate access to affordable and innovative medicines because Good Health Can\xe2\x80\x99t Wait.We started in 1984 with a modest investment, 20 employees and a bold vision. Today, we have research and development centres, manufacturing facilities or a commercial presence in 66 countries.For nearly four decades, we have stood for access, affordability and innovation based on the bedrock of deep science, progressive people practices and robust corporate governance. As the pharmaceutical industry evolves and undergoes disruption, we see an opportunity \xe2\x80\x93 to strengthen our core further (the next steps) and to build the future (the new bets).\xe2\x80\x98The Next and the New\xe2\x80\x99 is how we aim to continue to be the partner of choice \xe2\x80\x93 purpose-driven, future-ready and sustainable. Our aim is to reach over 1.5 Bn+ patients across the world by 2030 by growing our core businesses and building for the future with sustainability at the core of our purpose and strategy. Sustainability for us means operating in a manner that respects people, planet and purpose \xe2\x80\x93 helping us conserve precious resources, serve our patients, create value for stakeholders, give back to society, fulfil our potential and maintain our integrity and transparencyDr Reddy\xe2\x80\x99s maintains a work environment, free from discrimination and is an equal opportunity employer. We are committed to employ & nurture all qualified diverse workforce without regard to race, colour religion, nationality, sex, age, disability status, genetics, sexual orientation, gender expression, citizenship or any other characteristic or classification protected by applicable law(s) of the country we operate in. We treasure every talent, and recognize merit and diversity in our organization.Job Summary
We are looking for a candidate to ensure the efficient execution of production plans for input mateial viz., Raw material, Packing material, Consumbles, Resin etc., coordinating with cross-functional teams. The role involves converting purchase requestion to process orders, preparing monthly reports, and ensuring adherence to safety and quality norms.Roles & Responsibilities
The team member is primarily responsible for managing input material, viz., raw material, packing material, resin, and consumables for the biologic plant. To manage inventory management and coordinate with individuals and cross-functional teams on material planning. To interact with the procurement team, development team, and program team t to ensure proper planning for existing commercial products and new products in the pipe lines.The team member must meet the full kitting of input material and safety stock levels. Consultation with production schedulers for the changes in the production schedule for inventory planning Review material issuance variances against standard usage. Monitor all BOM changes and update the respective systems on a regular basis. Review of non-moving, near expiry and under test materials.The team member responsibilities include developing the plan most effectively and efficiently for input material planning, meeting the production plan, and Target inventory. Implement and maintain inventory management strategies for all raw materials, packing materials, and Consumables by regular review and optimisation of inventory parameters and levels (e.g., reorder point, safety stock, ABC categorization).The team member acts as an interface between production, QC, and procurement to resolve material planning-related issues. Place purchase requests based on the production plan / campaign plan. Regular review of planned orders, purchase requests, and purchase orders Consultation with the procurement team regarding the availability of inventory as per the production schedule Consultation with Production Schedulers for the changes in the Production Schedule for Inventory PlanningA review of non-moving and slow-moving inventory recommends actions to move the stock. Tracking with QC regarding the release of materials and retesting of materials for production usage. Accountable for master data management in SAP, Kinaxis, and digital plant form for raw materials, packing materials, and consumables.Ensure full kitting for input material as against plan published.QualificationsEducational qualification: A Bachelor\'s or Master\xe2\x80\x99s degree in Engineering, Operations Management, or a related fieldMinimum work experience: 5 to 8 years of experience in production planning, execution, and coordination in a manufacturing environment, with a focus on safety and complianceSkills & attributes:Technical Skills

• Knowledge of regulatory requirements and safety standards, and familiarity with industry standards for safety norms, company policies and procedures.
• Experience in achieving production plans, and ensuring machine and material availability.
• Problem solving experience in resource handling and product schedule planning based on urgency.
• Proficiency in documentation of daily meetings, and preparation of MIS reports, production plans and packing plans.
• Familiarity with MES software, specifically the elements of process orders.

Behavioural Skills

• Strong communication skills and collaborative mind set to coordinate with cross-functional teams.
• Effective problem-solving and decision-making skills to address production-related issues, prioritize tasks, and make decisions based on urgency.
• Flexibility to adapt to changing production priorities, scheduling requirements, and unforeseen challenges.
• Strong attention to detail for the preparation of production related documentation.
• Commitment to adherence and compliance with safety and quality norms.
• Taking initiative in resolving issues, improving processes, and contributing to the overall efficiency of production operations.
• Knowledge of working in regulatory environment like USFDA, MHRA, TGA
• Should have good understanding of cGM, cGDP, and good laboratories practice
• Must have hands-on experience in sophisticated manufacturing machine and equipment.

Additional InformationAbout the Department
Global Manufacturing Organisation (GMO)
At Dr. Reddy\'s 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 1,150+ drug master files across key therapy areas such as Oncology, Cardio-vascular, Central Nervous System and Anti-Diabetes. he 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 \xe2\x80\x98factories of the future\xe2\x80\x99 is integral to innovation and to build healthcare of the future.Benefits Offered
At Dr. Reddy\xe2\x80\x99s we actively help to catalyse your career growth and professional development through personalised learning programs.
The benefits you will enjoy at Dr. Reddy\xe2\x80\x99s 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. Reddy\xe2\x80\x99s why they come to work every day and they\xe2\x80\x99ll say, because Good Health Can\xe2\x80\x99t 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 we\xe2\x80\x99re 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 https://careers.drreddys.com/#!/

Dr. Reddy\'s Laboratories