Junior Process Engineer

Description

Job Summary: We are seeking a professional to generate, update, and manage operational documentation, ensure compliance with quality and safety standards, and lead investigations in pharmaceutical manufacturing. Key Highlights: 1. Generation and administration of operational documentation and the Quality Management System. 2. Leadership in manufacturing investigations and CAPA tracking. 3. SAP usage for inventory management and production orders. **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 legacy of deep science 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 sustainability initiatives, we published our first Sustainability Report in 2004\. Our current ESG goals aim to set a high standard 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 healthcare solutions not only as scientific formulations but also as means to help patients live healthier lives, and we remain constantly attentive to what is new and what lies ahead—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 been supported by an empowering environment that fosters individual capability while simultaneously promoting teamwork and shared success. We believe that when people with diverse skills unite around a common purpose and shared values, they can create 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 highly interested in finding the best candidate for this role and are open to exploring candidates from diverse backgrounds. For more details, please 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 will enjoy at Dr. Reddy's are on par with the industry’s best standards. **Job Description** **Key Responsibilities:** * Generate, update, and/or participate in developing documents required for Plant operations as defined by the Quality Management System or Safety guidelines used within the Production Department. * Stay trained on Safety and Quality Management System procedures governing operations, with the objective of preventing and identifying compliance deficiencies at the Plant. * Request and manage raw materials, reagents, solvents, and other materials required for product manufacturing, maintaining the minimum necessary inventory in the Production area via administration of production orders (creation, release, maintenance, confirmation, and closure) in SAP. * Maintain up-to-date Bills of Materials (BOM) and process times for accurate product costing and proper scheduling of requirements at the start of each campaign. * Administer the request, delivery, and review of documentation inherent to manufacturing processes, including manufacturing instructions, cleaning instructions, equipment usage logs, and various forms required to sustain uninterrupted Plant operations. * Develop training materials and ensure ongoing training of operational staff on the operations and processes in which they participate. * Verify, through on-site 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. * Track CAPAs arising from the Quality Management System, such as audits, deviations, change requests, risk assessments, annual reviews, etc. * Track CAPAs arising from the Safety Management System and promote compliance with safety training programs. * Prepare and track purchase requisitions for various materials required to sustain uninterrupted Plant operations. **Requirements** **Education:** * Chemical Engineering or related field (degree holder) **Experience:** * Minimum 2 years in Production * Statistical Process Control * Quality Management Systems * Proficiency in GMPs * Industrial Safety concepts * Production process analysis * Pharmaceutical manufacturing equipment