Regeneron is founded on the belief that the right idea, combined with the right team, can lead to significant transformations. Our growing global network is dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. In doing so, we are pioneering innovative approaches to science, manufacturing, and commercialization, as well as redefining our understanding of health. As a highly motivated Senior Functional Product Owner at Regeneron, you will be responsible for supporting both US and international operations with expertise in Workday HCM solutions, particularly in Compensation, Advanced Compensation, and Benefits modules. Your role will require a combination of technical competence, functional product design expertise, and strong collaboration skills to deliver impactful solutions. **Key Responsibilities:** - Act as the subject matter expert for Workday modules, focusing on Total Rewards (Compensation, Advanced Compensation), Benefits, and Time Tracking & Absence. - Collaborate with stakeholders to build product roadmaps and design innovative, scalable solutions that align with business needs. - Partner with business teams to capture requirements, document processes, and translate them into technical solutions. - Lead system-specific implementations, including integrations with third-party vendors for benefits solutions. - Be responsible for quality assurance testing, support user acceptance testing (UAT), and ensure timely delivery of solutions. - Provide hyper-care support after go-live, troubleshoot issues, and ensure smooth transitions. - Work closely with IT, boundary systems, and other technical teams to deliver effective solutions. - Identify gaps in existing processes and recommend improvements to enhance efficiency and scalability. - Build and maintain strong relationships with internal customers, keeping them informed of progress, risks, and delivery timelines. **Qualifications Required:** - 8+ years of HR functional lead experience, with a strong background in Workday HCM. - 6+ years of hands-on experience in Workday Compensation and Advanced Compensation modules, including supporting annual compensation cycles. - Experience with Workday Benefits modules, including integrations with third-party vendors. - Proficiency in creating advanced Workday reports and understanding security configurations for functional modules. - Exposure to other Workday modules like Time & Absence is a plus. - Strong understanding of system design, implementation, and integration processes. - Familiarity with ServiceNow or similar cloud-based applications is an advantage. - Experience documenting business processes, system flowcharts, and testing traceability (SIT, UAT). - Excellent communication and collaboration skills. - Analytical mindset with a proactive approach to problem-solving. - Ability to challenge and influence technical designs for simplicity and scalability. - Strong organizational skills with the ability to prioritize tasks and manage multiple priorities effectively. - Bachelors Degree is required. - Certifications in cloud-based technologies (e.g., Workday, AWS, ServiceNow) are a plus. If this opportunity excites you and you resonate with our vision, apply now to take your first step towards living the Regeneron Way! Regeneron offers an inclusive culture with comprehensive benefits that may vary by location, including health and wellness programs, 401(k) company match, equity awards, paid time off, and more. For additional information about Regeneron benefits, please visit [Regeneron Total Rewards](https://careers.regeneron.com/en/working-at-regeneron/total-rewards/).,
As a motivated individual, you will play a crucial role in supporting cGMP compliance within procurement operations at Regeneron. Your responsibilities will include investigating deviations, supporting CAPAs, coordinating supplier audits, handling change controls, and contributing to the development and implementation of the Supplier Corrective Action Report (SCAR) process. **Role Overview:** You will be essential in ensuring successful audit closures by proactively addressing issues with suppliers and maintaining clear communication to achieve satisfactory outcomes. Additionally, you will manage SCARs, follow up with suppliers and internal team members, and ensure timely reporting and closure of all actions. Your partnership with team members will facilitate discussions on Quality and Compliance, align category priorities with Procurement management, and achieve interpersonal goals. You will implement strategies to enhance process efficiency, drive value across procurement operations, and utilize your knowledge of global procurement processes within the biopharmaceutical industry to support the growth of the Global Procurement organization. **Key Responsibilities:** - Ensuring successful audit closures and maintaining clear communication with suppliers - Managing SCARs, following up with suppliers and internal team members, and ensuring timely reporting and closure of all actions - Partnering with team members to facilitate discussions on Quality and Compliance and aligning category priorities with Procurement management goals - Implementing strategies to improve process efficiency and drive value across end-to-end procurement operations - Applying in-depth knowledge of global procurement processes within the biopharmaceutical industry - Contributing to quality and compliance initiatives to maintain adherence to GxP standards and relevant regulatory requirements - Demonstrating data insights to guide decisions and deliver successful quality and compliance outcomes **Qualifications Required:** - Bachelor's degree in a relevant field and at least 8 years of experience in a cGMP environment focusing on quality, compliance, and/or procurement, with specific experience in the Pharma/BioPharma sector - Proven record in supporting global quality or category teams, processes, and suppliers across diverse categories - Strong relationships with customers and suppliers to achieve impactful results - Success in supporting cross-functional teams in areas such as SCARs, ASLs, CAPAs, Change Notifications, and other Quality and Compliance processes - Valuable insights and expertise in handling Quality and Compliance processes successfully - Ability to apply external data, market trends, and supplier engagement to enhance understanding of supply market dynamics - Experience operating with integrity, focus, and transparency in ambiguous environments to drive relevant change and improvement - Familiarity with quality and compliance electronic tools/systems is beneficial - Proficiency in standard business applications such as Word, Excel, and PowerPoint for communication, presentations, and analysis - Continuous improvement approach and collaboration with leadership to implement solutions If you meet the above qualifications and are eager to contribute to the future of healthcare at Regeneron, we encourage you to apply and take the first step towards living the Regeneron Way!,
You will be the Senior Manager Buyer at Regeneron's Global Procurement Capability Center in Bengaluru, playing a crucial role in establishing and leading a new team within the Capability Center. Your responsibilities will include overseeing the procurement workflow process for goods, supplies, and services requisitions within assigned business units or spending categories. You will focus on ensuring consistency, scalability, and efficiency in procurement processes while fostering capability development across Global Procurement. Collaboration with global colleagues to implement innovative and standardized ways of working will also be a key aspect of your role. **Key Responsibilities:** - Manage a team of Buyers within the Global Procurement Operations team to support Global Procurement and business stakeholders. - Develop standard methodologies and processes for purchase requisition (PR) and purchase order (PO) workflows. - Ensure all purchase requisitions (PRs) meet objectives and include vital documentation such as Comp Driven Exceptions (CBEs), quotes, Approved Supplier List (ASL) waivers, and New Supplier Request Forms. - Supervise adherence to contract policies, ensuring POs reference existing contracts, MSAs, or SOWs, and escalate to the Sourcing team for missing or expired contracts. - Provide mentorship, performance feedback, and career development guidance to direct reports. **Qualifications Required:** - Bachelor's degree in a relevant field with at least 8 years of dynamic experience in procurement. - Shown success in leading teams and processes across diverse categories. - Strong relationship-building skills to influence stakeholders and get results. - Proficiency with procurement tools, ERP systems (e.g., Oracle, Zycus), and eRFx platforms. - Strong communication and partner education skills regarding sourcing processes. If you are looking for an opportunity to lead and innovate in the procurement space, collaborate with global colleagues, and drive efficiency in procurement processes, this role at Regeneron might be the perfect fit for you. Apply now to take the first step towards shaping the future of healthcare with us.,
As a Senior AI/ML Engineer at Regeneron, you will be an integral part of the team, focusing on hands-on engineering and development work to drive the creation and implementation of artificial intelligence solutions in various research and development projects. Your responsibilities will include: - Designing, developing, and deploying AI models, algorithms, and solutions for analyzing complex biological and pharmaceutical data. - Collaborating with multi-functional teams to identify AI opportunities and contribute to project goals and requirements. - Creating and maintaining machine learning models, developing advanced algorithms for tasks like image analysis and natural language processing. - Enforcing standards in AI model development and deployment, ensuring performance, scalability, reliability, and regulatory compliance. - Staying updated with the latest AI advancements, evaluating their potential applications, and fostering innovation within the organization. - Engaging with external partners to integrate modern AI technologies and tools. - Sharing insights and findings in AI-related discussions with stakeholders. - Optimizing AI models for performance and reliability while considering computational and regulatory constraints. - Participating in scientific and technical discussions and communicating findings effectively to various audiences. - Developing and maintaining comprehensive documentation for AI models and systems. - Communicating sophisticated AI concepts to non-technical stakeholders. Qualifications required for this role include: - Bachelor's, Master's, or Ph.D. degree in Computer Science, Artificial Intelligence, Data Science, or a related field. - At least 2 years of experience in AI/ML engineering, preferably in the biotechnology, pharmaceutical, or healthcare industry. - Hands-on experience in building LLMs/Generative AI solutions from scratch using frameworks such as Lang Chain, LangGraph, Crew. - Proficient programming skills in Python, R, or Java, along with familiarity with software engineering practices. - Practical experience in developing and deploying AI models for production-grade conversational AI systems. - Experience in RAG systems, knowledge base integration with LLMs, prompt engineering, and techniques for improving model performance. - Knowledge of cloud platforms like AWS, Azure, GCP, and their AI services. - Strong problem-solving skills, results-driven approach, and excellent communication skills. - Understanding of regulatory compliance related to AI in the biotech and pharma industries. - Profound knowledge of machine learning algorithms, deep learning frameworks (e.g., TensorFlow, PyTorch), and statistical methods. - Familiarity with natural language processing techniques and tools, big data technologies like Hadoop, Spark, or NoSQL databases. If you are passionate about AI research and advancements, have a collaborative mindset, and possess the required qualifications, apply now to join Regeneron in crafting the future of healthcare.,
Job Role: Principal Investigator – Medicinal Chemistry (Integrated Drug Discovery) Job location: Hyderabad At Syngene, safety is at the heart of everything we do personally and professionally. Syngene has placed safety at par with business performance with shared responsibility and accountability, including following safety guidelines, procedures and SOPs, in letter and spirit Mandatory expectation for all roles as per Syngene safety guidelines: Overall adherence to safe practices and procedures of oneself and the teams aligned. Contributing to development of procedures, practices and systems that ensures safe operations and compliance to company’s integrity & quality standards. Driving a corporate culture that promotes environment, health, and safety (EHS) mindset and operational discipline at the workplace at all times. Ensuring safety of self, teams and lab/plant by adhering to safety protocols and following environment, health, and safety (EHS) requirements at all times in the workplace. Ensure all assigned mandatory trainings related to data integrity, health, and safety measures are completed on time by all members of the team including self-Compliance to Syngene’ s quality standards at all times. Hold self and their teams accountable for the achievement of safety goals Govern and Review safety metrics from time to time. Job Purpose Provide strategic and scientific leadership to integrated drug discovery projects for our clients. Liaise with the Functional Head - Medicinal Chemistry on projects priorities and ensure that project deliverables are met. As program leader supervise medicinal chemistry project(s). Analyze SAR and design new set of compounds using Comp Chem tools to address various Med Chem issues. Provide regular updates on project progress to the Section Head - medicinal chemistry / Functional Leads and clients. Work collaboratively with the CADD scientists, biologists, DMPK scientists and the safety pharmacologists. Exceptional creativity and innovation in the genuine spirit of collaboration Core commitment to safety, integrity, compliance, quality, and service. Key Responsibilities Candidate should have a minimum of 6 - 10 yrs. experience in drug discovery from pharmaceutical or biotech industry. Excellent understanding of the concepts of drug discovery, preferably having prior experience of progressing a project from hit identification to lead optimization. Has prior experience working with a cross-functional team, comprising assay biologists, Structural biologists, DMPK scientists, computational chemists, and safety pharmacologists. Familiarity with molecular modelling concepts and tools is desirable. Strong knowledge of data analysis (SAR/SPR) and informatics tools. Familiarity with cGMP and regulatory knowledge. Strong Client communication and presentation skills. Extensive knowledge and experience in synthesis planning, synthetic methods and use of modern chromatographic and analytical tools. Proven ability to lead and motivate the teams. Excellent written and verbal communication skills. A team player / works well in multi-discipline teams Builds strong plans to provide clarity for others, and utilizes time management tools and capabilities. Educational Qualification Ph.D./PDF in Organic /Medicinal Chemistry or relevant field. Technical / Functional Skills Possess a very high scientific capability. Knowledge of route scouting. Sound knowledge of Process safety and hazard evaluation. Excellent cGMP and regulatory knowledge. Strong knowledge of Data analysis software. Strong Client communication skills. Cross-departmental interaction. Experience: Minimum 6-9 years of experience for Ph.D / Post Doc Behavioural Skills Sound interpersonal skills. Good Team skills T ime Management skills Strong system thinking and trouble shooting ability. Sound leadership Equal Opportunity Employer It is the policy of Syngene to provide equal employment opportunity (EEO) to all persons regardless of age, color, national origin, citizenship status, physical or mental disability, race, religion, creed, gender, sex, sexual orientation, gender identity and/or expression, genetic information, marital status, status with regard to public assistance, veteran status, or any other characteristic protected by applicable legislation or local law. In addition, Syngene will provide reasonable accommodations for qualified individuals with disabilities
You will join Regeneron, a company dedicated to inventing, developing, and commercializing medicines that change lives for those with serious diseases. Your role will involve supporting cGMP compliance within procurement operations by assisting with various key activities. **Role Overview:** As part of the team, you will be responsible for ensuring successful audit closures, managing Supplier Corrective Action Reports (SCARs), partnering with team members for Quality and Compliance discussions, implementing process efficiency strategies, and contributing to maintaining adherence to regulatory requirements. **Key Responsibilities:** - Proactively address issues to achieve successful audit closures and maintain clear communication with suppliers - Manage SCARs, follow up with suppliers and internal team members, and ensure timely reporting and closure of actions - Partner closely with team members to align category priorities with Procurement management goals - Implement strategies to improve process efficiency and drive value across end-to-end procurement operations - Support quality and compliance initiatives to maintain adherence to relevant regulatory requirements - Demonstrate data insights to guide decisions and deliver successful quality and compliance outcomes **Qualifications Required:** - Bachelor's degree in a relevant field and at least 8 years of experience in a cGMP environment - Experience in supporting global quality or category teams, processes, and suppliers - Strong relationship-building skills with customers and suppliers - Success in supporting cross-functional teams in areas such as SCARs, ASLs, CAPAs, and Change Notifications - Proficiency in standard business applications such as Word, Excel, and PowerPoint - Continuous improvement approach with the ability to find opportunities for enhancement If you have the required qualifications and experience, apply now to be a part of Regeneron's inclusive culture and take the first step towards living the Regeneron Way. Visit the Regeneron careers website for more information on benefits and rewards.,
As a Senior Specialist Contracting at Regeneron's Global Procurement Capability Centre in Bengaluru, you will be responsible for demonstrating an efficient approach to buying goods and services and ensuring effective contract execution using procurement applications. Your role will contribute to maintaining consistency, scalability, and efficiency for repeatable, location-agnostic contracting across Global Procurement. Working closely with colleagues globally, you will support the end-to-end contract execution process by implementing category strategy, negotiating supplier terms, and providing analytical insights for future decision-making. **Key Responsibilities:** - Draft and finalize contracts across categories and services within agreed quality and timelines - Support simple contracting activities to ensure compliance with relevant regulations - Align contracting approach with category strategy in coordination with colleagues in Global Procurement - Implement contracting approaches aligned with category strategies to meet global and regional business needs - Support simple negotiations, supplier management activities, and stakeholder engagement for assigned contracts - Identify and implement process efficiencies within contracting approaches across Global Procurement - Drive value through cost savings, cash flow improvement, and efficiency savings from contract management activities **Qualifications Required:** - 8+ years of experience in procurement contracts - Bachelor's degree in a relevant field of study - Progressive experience in procurement, including exposure to the Pharma/BioPharma sector - Ability to establish relationships with stakeholders and suppliers - Proficiency in supporting cross-functional teams in implementing category strategies - Knowledge of rates, unit costs, and costing structures for efficient negotiations - Experience in using external data sources, market information, and supplier engagement to support negotiation strategy - Integrity, focus, and clarity in leading change and improvement in an ambiguous environment - Solid understanding of sourcing contracting tools, ERPs, and eRFx systems (Oracle, Zycus, Ariba, Other) - Proficiency in standard business applications for communication, presentation, and analysis (Word, Excel, PowerPoint) Regeneron's inclusive culture offers comprehensive benefits that vary by location, including health and wellness programs, fitness centers, equity awards, annual bonuses, paid time off, and more. If you are interested in crafting the future of healthcare and possess the required qualifications, apply now to join Regeneron. For more information on benefits specific to your location, speak with your recruiter. Please note that certain background checks will be conducted as part of the recruitment process in accordance with local laws and regulations.,