Job Summary: We are seeking a Chemical Engineer or related professional for a position in the Production area, responsible for generating and maintaining operational documentation, administering materials, updating bills of materials, and leading investigations to ensure compliance with quality and safety systems. Key Highlights: 1. Generation and updating of operational documentation 2. Administration of raw materials and production materials in SAP 3. Leadership in quality and safety investigations **Company Description** **Who We Are?** Dr. Reddy's is a global pharmaceutical company headquartered in Hyderabad, India. Driven by our purpose of "Good health cannot wait", we work to deliver accessible and innovative medicines. We offer a portfolio of products and services including active pharmaceutical ingredients, generics, biosimilars, and over-the-counter medications. Our key markets include the U.S., India, Russia and other Commonwealth of Independent States countries, China, Brazil, and Europe. As a company with a deep-rooted scientific heritage that has led to several industry firsts, we continue to plan ahead and invest in future growth drivers such as access to novel molecules, digital therapeutics, and consumer healthcare. As pioneers in adopting sustainability initiatives, we published our first Sustainability Report in 2004. Our current ESG goals aim to set high standards in environmental management; patient access and affordability; diversity; and governance. **Our Work Culture** Ask any Dr. Reddy's employee why they come to work every day, and they will tell you: because good health cannot wait. This is our creed, as well as the guiding principle behind all our actions. We view health solutions not only as scientific formulations but also as a means to help patients lead healthier lives, and we are always attuned to what’s new and what’s next—empowering our employees to stay at the forefront. To achieve this, we foster a culture of empathy and dynamism. Our employees have been at the center of our journey over the past decades. They have benefited from an empowering environment that drives individual capability while simultaneously promoting teamwork and shared success. We believe that when people with diverse skills unite around a common purpose and value system, they can work magic. **Diversity, Equity & Inclusion** At Dr. Reddy's, we are deeply committed to building a diverse, equitable, and inclusive workplace where everyone belongs and is valued for their contributions to the team. We are keen to identify the best candidate for this role and remain open to exploring candidates from diverse backgrounds. For more details, visit our careers website at https://careers.drreddys.com/\#!/ **Benefits Offered** At Dr. Reddy's, we actively support your professional growth and development through customized learning programs. The benefits you’ll enjoy at Dr. Reddy's are on par with the industry’s best standards. **Job Description** **Key Responsibilities:** * Generate, update, and/or participate in preparing documents required for Plant operations as stipulated in the Quality Management System or Safety guidelines applicable to the Production Department. * Maintain up-to-date training on Safety procedures and the Quality Management System governing operations, with the objective of preventing and identifying compliance gaps at the Plant. * Request and administer raw materials, reagents, solvents, and other materials required for product manufacturing, maintaining minimum necessary inventory levels in the Production area through administration of production orders (creation, release, maintenance, confirmation, and closure) in SAP. * Keep bills of materials (BOM) and process times updated for accurate product costing and proper scheduling of requirements at the start of each campaign. * Administer the request, delivery, and review of documentation intrinsic to manufacturing processes—including manufacturing instructions, cleaning instructions, equipment usage sheets, and various forms—to ensure continuity of Plant operations. * Develop training materials and maintain current training for operational staff on the operations and processes in which they participate. * Verify, via Plant supervision, that processes are executed per documented procedures and that recordkeeping complies with the ALCOA principles. * Lead investigation processes related to RFEs, RFTs, and incidents recorded during manufacturing. * Follow up on CAPAs arising from the Quality Management System, including audits, deviations, change requests, risk assessments, annual reviews, etc. * Follow up on CAPAs arising from the Safety Management System and promote compliance with safety training programs. * Prepare and follow up on purchase requisitions for various materials required to sustain Plant operations. **Requirements** **Education:** * Chemical Engineering or related discipline (degree holder) **Experience:** * Minimum 2 years in Production * Statistical Process Control * Quality Management Systems * GMP proficiency * Industrial Safety concepts * Production process analysis * Pharmaceutical manufacturing equipment