368 Manufacturing Analysis Jobs in Hyderabad

Job Title: Deputy Manager - Process Engineering (Vehicle Assembly)Location: Open to all citiesExperience Level: 3-10 years Role Overview The Deputy Manager - Process Engineering conducts product feasibility, process flow analysis, and simulations using Delmia for vehicle assembly, providing critical feedback to R&D teams. This role drives assembly process planning, fixture design, virtual builds, and integration of stamping/manufacturing processes while implementing global TCF strategies and ensuring manufacturable designs. Emphasis on digitization, standardization, logistics layouts, and cross-functional project execution supports new product development. Key Responsibilities Perform product feasibility studies, process flow analysis, and Delmia simulations for vehicle assembly; deliver R&D feedback for design improvements. Design assembly fixtures, plan TCF manufacturing processes, and conduct virtual builds/studies for stamping and assembly optimization. Integrate functional areas, prepare manufacturing strategies, and develop logistics layouts for new projects; ensure part manufacturability. Lead process documentation, digitization initiatives, and standardization across project activities. Required Skills Proficiency in vehicle assembly, TCF manufacturing, assembly fixture design, process engineering, stamping, and Delmia simulation. Strong cross-functional collaboration, project planning, and lean manufacturing for automotive production. Qualifications Education: B.E. in Mechanical/Production Engineering. Experience: 3-10 years in automotive process engineering. Interview: Enrichment AI Interview Agentic.

Role Overview: As a Senior Quality Assurance Professional at PKL LIMITED, you will play a pivotal role in strengthening the QA function by leveraging your technical expertise, manufacturing experience, and leadership skills. Your main responsibilities will include ensuring compliance with various statutory standards, leading audits, overseeing quality initiatives, and driving continuous improvement efforts across the organization. Key Responsibilities: - Ensure strict adherence to ISO, BIS, PESO, and other statutory/regulatory requirements. - Lead internal and external audits, customer audits, and certification processes. - Oversee documentation, process standardization, and system improvements in alignment with QMS requirements. - Supervise inspection teams for raw materials, components, and finished products. - Ensure calibration of measuring instruments and maintenance of calibration records. - Lead Root Cause Analysis (RCA) and drive Corrective & Preventive Actions (CAPA). - Implement continuous improvement initiatives to enhance product quality and reduce rejections/returns. - Interact with customers for quality clarifications, audits, approvals, and complaint resolution. - Support vendor development activities and ensure supplier quality compliance. - Provide guidance to junior QA/QC staff and contribute to team capability development. Qualifications Required: - B.Tech in Mechanical/Metallurgy/Production/Industrial Engineering or a relevant field. - 6-8 years of experience in manufacturing QA/QC, with at least 2-3 years in a leadership or senior role. - Strong knowledge of engineering drawings, welding standards, and manufacturing inspection methods. - Proficiency in ERP systems, MS Office, and preparation of QA reports. - Preferred certifications: ISO 9001 Internal Auditor, Six Sigma (Green Belt/Black Belt), NDT Level II. [No additional details about the company were provided in the job description.] Role Overview: As a Senior Quality Assurance Professional at PKL LIMITED, you will play a pivotal role in strengthening the QA function by leveraging your technical expertise, manufacturing experience, and leadership skills. Your main responsibilities will include ensuring compliance with various statutory standards, leading audits, overseeing quality initiatives, and driving continuous improvement efforts across the organization. Key Responsibilities: - Ensure strict adherence to ISO, BIS, PESO, and other statutory/regulatory requirements. - Lead internal and external audits, customer audits, and certification processes. - Oversee documentation, process standardization, and system improvements in alignment with QMS requirements. - Supervise inspection teams for raw materials, components, and finished products. - Ensure calibration of measuring instruments and maintenance of calibration records. - Lead Root Cause Analysis (RCA) and drive Corrective & Preventive Actions (CAPA). - Implement continuous improvement initiatives to enhance product quality and reduce rejections/returns. - Interact with customers for quality clarifications, audits, approvals, and complaint resolution. - Support vendor development activities and ensure supplier quality compliance. - Provide guidance to junior QA/QC staff and contribute to team capability development. Qualifications Required: - B.Tech in Mechanical/Metallurgy/Production/Industrial Engineering or a relevant field. - 6-8 years of experience in manufacturing QA/QC, with at least 2-3 years in a leadership or senior role. - Strong knowledge of engineering drawings, welding standards, and manufacturing inspection methods. - Proficiency in ERP systems, MS Office, and preparation of QA reports. - Preferred certifications: ISO 9001 Internal Auditor, Six Sigma (Green Belt/Black Belt), NDT Level II. [No additional details about the company were provided in the job description.]

As a highly experienced Sales Manager with 15-20 years of US sales and Business Development experience, your role will involve enhancing brand reputation and driving business growth across the US geography. Your responsibilities will include: - Acting as a Sales manager to drive business development and sales initiatives - Adding new clients to the business portfolio - Being accountable for enterprise to enterprise sales - Managing P&L responsibilities for a specific geography - Developing strategic initiatives to capture market share - Implementing sales strategies to achieve performance milestones - Crafting market segmentation and penetration strategies - Conducting competitor analysis to stay informed of market trends - Optimizing resource utilization and cost savings - Defining business mission and aligning resources for optimal performance - Collaborating effectively with teams and demonstrating strong communication skills - Implementing leadership initiatives to drive growth in a dynamic business environment Desired Background/Skills: - Proven track record of teamwork - 2+ years of experience with Startups or consulting - Willingness to work flexible hours - Exposure to team management is preferred Good to have: - Understanding of US healthcare, finance and banking, retail, manufacturing, hi-tech verticals - Experience with B2C and B2B products This role offers the opportunity to leverage your extensive experience in US sales and business development to drive growth and success in a dynamic environment.,

As a Manufacturing Engineer, you will play a crucial role in evaluating and improving manufacturing processes to ensure efficiency and quality. Your responsibilities will include: - Conducting research programs to evaluate manufacturing processes - Designing and testing manufacturing methods and equipment - Analyzing workflow, space requirements, and equipment layout to enhance manufacturing efficiency - Designing testing methods to ensure product and process quality - Providing decision-making information by calculating production costs and reviewing schedules - Generating reports by collecting and analyzing information - Maintaining equipment operational and coordinating maintenance services - Writing computer programs and entering data to maintain product and process database - Contributing to team efforts to achieve desired results Your qualifications for this role should include: - Bachelor's degree in Engineering (B.Tech preferred) - 6-10 years of experience in manufacturing engineering - Strong knowledge of product design, fabrication, assembly, tooling, and materials - Ability to work collaboratively in a team environment - Excellent problem-solving and decision-making skills Please note: Additional details about the company were not provided in the job description.,

As an Oracle Cloud Process Manufacturing Consultant, you will be responsible for the following: - Implementing Oracle Cloud Process Manufacturing and Cost Management with expertise - Demonstrating experience in integrations, both Inbound and Outbound - Collaborating effectively with team members across different tracks - Reporting progress to the offshore team lead and directly engaging with onshore team members and clients when necessary - Assisting the technical team with conversions, integrations, and custom reports - Capable of comprehending and developing business requirements and functional specification documents - Generating essential artifacts like fit gap documents, configuration documents, functional specifications, test scripts, and training documents - Possessing strong oral and written communication skills - Conducting Fusion Application Configuration, Testing, Bug Fixes, Solution Designs, and Fit Gap Analysis Qualifications required for this role: - Proficiency in Oracle Cloud Process Manufacturing and Cost Management implementation - Experience in Oracle Cloud integrations - Strong communication skills - Ability to create various project-related documents ,

Manufacturing Head Key Responsibilities Machining Operations Cycle Time Optimization Oversee and manage all aspects of the machine shop, including CNC turning, milling (3-axis, 5-axis), grinding, and other finishing operations. Drive continuous improvement in cycle times, machine utilization, and tooling life. Ensure the effective scheduling and loading of CNC and conventional machines to meet production deadlines and optimize throughput. Approve and implement process sheets, tooling selection, and CNC programs (working closely with the programming team). Quality, Precision, Metrology Champion the achievement of tight tolerance standards critical to the parts produced. Oversee the Quality Management System and Metrology lab, ensuring calibration and effective use of CMMs, surface finish testers, and other precision measurement tools. Drastically reduce scrap and rework rates (PPM) by implementing robust root cause analysis and process controls. Equipment Maintenance Asset Management Develop and manage Total Productive Maintenance (TPM) programs for high-value CNC machines, VMCs, HMCs, and complex grinding equipment to maximize uptime. Financial Budget Management Develop and manage the annual budget, focusing on controlling costs related to tooling, machine maintenance, utilities, and direct labor hours per part. Analyze costs per part, identifying opportunities for material savings and process efficiencies (e.g., minimizing material wastage/chips). Leadership, Safety, Compliance Lead and mentor the team, including Production Supervisors, CNC Programmers, Quality Engineers, and skilled Machinists. Enforce strict adherence to safety protocols, particularly related to machine guarding, chip management, and handling of oils/coolants. Required Qualifications Skills Education: Bachelor's degree in Mechanical/Production Engineering If interested, Please share your updated CV - hrjobsconsultancy1@gmail.com

Chemical Engineers, or Process Engineers, oversee the process of converting raw materials into new products in fields such as environmental conservation, pharmaceuticals, biotechnology, energy and consumer manufacturing. Their duties include designing procedures to isolate different chemical elements and reconfigure them, testing the resulting products and designing equipment setups for optimal safety and efficiency. Chemical Engineer duties and responsibilities Chemical Engineers perform many scientific and technical related to the process of manufacturing products. Some of their typical duties and responsibilities include: Developing manufacturing processes that minimize waste and increase the quality of finished products Monitoring and testing processes and products found in all phases of production Developing and implementing safety procedures for staff working with hazardous materials Designing, planning and implementing the layout of manufacturing equipment to optimize production and decrease costs Staying up to date with new and emerging manufacturing processes Creating and presenting cost analysis reports to upper management

A Manufacturing Engineer is responsible for designing, implementing, and optimizing manufacturing processes to ensure the efficient, safe, and cost-effective production of goods. The role involves working to improve existing systems, designing new ones, and ensuring products meet quality and safety standards. The specific duties and required qualifications vary significantly based on the experience level of the position, ranging from entry-level technician roles to senior engineering leadership. Typical duties and responsibilitiesEvaluate and improve processes: Analyze current manufacturing workflows, equipment, and production methods to identify inefficiencies and areas for improvement. This often involves applying continuous improvement techniques like Lean Manufacturing, Six Sigma, and Kaizen.Design and develop systems: Design new manufacturing processes, tools, and equipment for new products or to upgrade existing ones. This may include designing factory or production line layouts.Ensure quality control: Develop, implement, and monitor quality control processes and testing methods to maintain product standards and reduce defect rates.Manage costs and efficiency: Calculate production, labor, and material costs to help management make better business decisions and implement cost-saving measures.Collaborate with teams: Work closely with cross-functional teams, including design engineers, quality control, maintenance, and production staff, to ensure seamless execution of manufacturing strategies.Maintain equipment: Coordinate maintenance and repair services for manufacturing equipment to ensure it remains operational, and train technicians on new or existing equipment.Document procedures: Create and maintain technical documentation for manufacturing processes, including work instructions, standard operating procedures (SOPs), and flow charts.Adhere to regulations: Ensure all manufacturing procedures and equipment comply with safety standards and government regulations. If you're interested, Kindly forward your resume to:- prajapatimaity05@gmail.com

We are looking for a highly capable manufacturing technician to join our business's production division. You will be assembling product components, documenting production information, and performing routine maintenance on equipment and machinery. To ensure success as a manufacturing technician, you should possess extensive knowledge of product assembly and experience in a similar industry. A first-class manufacturing technician will be someone whose production knowledge and skills result in the manufacturing of high-quality products. Manufacturing Technician Responsibilities: Performing assigned product manufacturing and assembly tasks. Conducting quality checks on the functionality of parts and components. Adding finishing touches to the appearance of components. Optimizing production efficiency by adjusting machinery and equipment settings as needed. Performing minor repairs and reporting breakdowns in a timely manner. Keeping equipment maintenance logs, as well as maintaining a safe and tidy work environment. Updating productivity records and writing incident reports, if relevant. Training and supervising new employees. Collaborating with other departments to complete production orders on time. Complying with internal policies and industry regulations.

We are looking for an experienced Process Engineer to be responsible for the process design, operation and implementation. The successful candidate will be able to improve industrial processes in order to maintain efficiency, reduce cost, improve sustainability and maximize profitability. Responsibilities Develop, configure and optimize industrial processes from inception through to start up and certification Assess processes, take measurements and interpret data Design, run, test and upgrade systems and processes Develop best practices, routines and innovative solutions to improve production rates and quality of output Perform process simulations Manage cost and time constraints Perform risk assessments Provide process documentation and operating instructions  

You are an experienced Factory Manager who will be responsible for overseeing the mattress manufacturing facility in Hyderabad. Your role will include ensuring smooth plant operations, maintaining high quality standards, optimizing productivity, and effectively managing a large workforce. It is essential for you to have experience in handling the P&L of a factory. **Key Responsibilities:** - Oversee end-to-end plant operations including production, maintenance, quality, and dispatch. - Plan, organize, and monitor production schedules to ensure timely and cost-effective delivery. - Implement lean manufacturing practices to improve efficiency and reduce wastage. - Ensure strict adherence to safety protocols, compliance requirements, and statutory regulations. - Lead, mentor, and manage factory staff to achieve operational and performance goals. - Collaborate with the supply chain team to ensure timely availability of raw materials. - Monitor and maintain product quality in line with company benchmarks and customer expectations. - Prepare and manage factory budgets, cost controls, and productivity reports. - Drive process improvements, automation initiatives, and industry best practices in manufacturing. - Take full ownership of the factory's P&L, ensuring financial performance aligns with business objectives. **Qualifications Required:** - Bachelor's degree in Mechanical/Industrial Engineering, Operations, or a related field. - 7-12 years of manufacturing experience, preferably in consumer goods, furniture, or the mattress/foam industry. - Proven experience managing mid-to-large scale manufacturing facilities. - Strong leadership, team management, and interpersonal skills. - Solid understanding of lean manufacturing, Kaizen, and quality management systems. - Prior experience in P&L management of a manufacturing unit is mandatory. - Hands-on, solutions-oriented approach with strong analytical and problem-solving skills. You will have the opportunity to work with one of India's fastest-growing sleep solutions brands and be part of a collaborative, innovation-driven, and people-first work environment.,

Role Overview: You will be responsible for designing and managing the development of modular, reusable, elegantly designed, and maintainable software or solutions that support the Manufacturing organization and other Cross Functional strategic initiatives. Your role will involve participating in fit-gap workshops with business stakeholders, providing effort estimates, and proposing solutions. You will be expected to be hands-on, solution-driven, and customer-focused. Additionally, you will develop and maintain code repositories, respond rapidly to bug reports or security vulnerability issues, and integrate software development best practices into your daily work. Key Responsibilities: - Design and manage the development of modular, reusable, elegantly designed, and maintainable software or solutions - Participate in fit-gap workshops, provide effort estimates, and propose solutions - Develop and maintain code repositories, and respond rapidly to bug reports or security vulnerability issues - Collaborate extensively with colleagues across different departments - Enable data needed for frontend applications on cloud platforms - Drive use cases on real-time and near real-time analytics, integrations with internal and external systems - Support moving manufacturing warehousing platforms to the cloud - Ensure delivered solutions adhere to architectural and development standards - Align designed solutions with Data and Analytics strategy standards and roadmap - Bring innovations to the solutions and add measurable values to the manufacturing business Qualifications Required: - 4+ years of previous relevant experience - Experience in customer-facing IT roles is a plus - Strong data engineering fundamentals in data management, data analysis, back-end system design - Hands-on exposure in Data & Analytics solutions (descriptive, diagnostic, predictive & prescriptive) - Previous AWS experience is preferred - Previous working experience in manufacturing business for a healthcare company is a plus - Previous working experience with D365 is a plus - Previous working experience in driving AI/ML projects is a plus - Familiarity with Agile, Disciplined Agile, as well as Waterfall delivery concepts - Ability to collect and interpret requirements and build supporting solutions to satisfy business requirements - Familiarity with Benefit Plus Cafeteria, Meal vouchers, Public Transportation allowance, MultiSport Card, and Employee Share Purchase Plan Please note that the additional details of the company were not explicitly mentioned in the provided job description.,

You will be responsible for providing operational support to business functions in managing contractors and external services, as well as representing an interface between the internal community and external partners. Acting as a single point of contact for all activities in accordance with legislation, internal regulations, good practices, and business objectives via NOCC Engineering project team. - Provide operational and administrative support to the organization in coordinating and managing external contractors, and activities between internal stakeholders and external partners. - Create purchase orders and order equipment in SAP/ESHOP. - Care for and maintain electronic databases (SharePoint). - Ensure consistency and quality of procedures and documentation by being the SPOC for the external service provider regarding operational processes related to external employees. - Support the T&L organization in defining training for external associates to obtain their qualifications. - Manage and review training roles for all external colleagues, monitor education, and ensure training consistency. - Send updated production documents to relevant external colleagues for education and knowledge transfer, including conducting training if necessary. - Support the implementation of external services according to defined KPIs. - 2+ years in a relevant role - Knowledge of Microsoft Office - Knowledge of SAP is recommended - Skills in Business Continuity, Business Networking, Change Control, Computer Science, Construction Management, Cost Management, Flexibility, General HSE Knowledge, HVAC, GDP, Installations, Capa, GMP, Relevant Tools and Systems, Manufacturing Production, Project Commissioning, Project Engineering, Project Execution, Risk Management, Root Cause Analysis, Total Productive Maintenance Novartis is committed to helping people with diseases and their families by fostering a community of smart, passionate individuals who collaborate, support, and inspire each other to achieve breakthroughs that change patients" lives. They offer a supportive work environment and diverse teams that are representative of the patients and communities they serve.,

Role Overview: As a Specialist Quality by Design (QbD) at Dr. Reddys Laboratories Ltd., based in Hyderabad, India, you will play a crucial role in implementing and maintaining QbD principles in pharmaceutical manufacturing processes. Your primary focus will be on ensuring high-quality products and regulatory compliance through the development and implementation of QbD strategies for both new and existing products. Collaborating with cross-functional teams, analyzing complex data sets, and providing technical expertise will be key responsibilities in this role. Key Responsibilities: - Develop and implement QbD strategies for new and existing products - Conduct risk assessments and design of experiments (DoE) to optimize manufacturing processes - Analyze and interpret complex data sets to identify critical quality attributes and process parameters - Collaborate with cross-functional teams to integrate QbD principles into product development and manufacturing - Develop and maintain documentation related to QbD initiatives, including risk assessment reports and control strategies - Provide technical expertise and training on QbD methodologies to team members - Monitor and evaluate the effectiveness of QbD implementation, recommending improvements as needed - Ensure compliance with regulatory requirements and industry standards related to QbD - Participate in regulatory inspections and audits, providing QbD-related information as required Qualifications: - Bachelor's or Master's degree in Chemical Engineering, Pharmaceutical Sciences, or a related field - 4-8 years of experience in QbD implementation within the pharmaceutical or biotechnology industry - Strong understanding of Quality by Design (QbD) principles and methodologies - Proficiency in statistical analysis, data interpretation, and risk assessment techniques - Experience with process analytical technology (PAT) and design of experiments (DoE) - In-depth knowledge of pharmaceutical manufacturing processes - Understanding of regulatory requirements (FDA, EMA) related to QbD implementation - Excellent problem-solving skills and attention to detail - Strong communication and collaboration abilities - Experience in process development and optimization - Proficiency in relevant software tools for data analysis and reporting - Certifications in Six Sigma or Lean Manufacturing (preferred),

As the Category/Merchandising Head at AEL or Group Companies, your role involves creating a category plan aligned with the organization's requirements and implementing it in coordination with the Business Unit (BU) strategy and teams. You will be responsible for maintaining key account management, brand alliances, and seller relationship management. Your key responsibilities will include: - Developing and implementing a category plan in alignment with the BU. - Managing key account relationships, brand alliances, and seller management. - Onboarding and maintaining new sellers and brands to enhance customer experience. - Building assortment, monitoring pricing and inventory according to sales and margin plans. - Identifying trends and onboarding new assortments per seasonal planning. - Leading consumer experience through product quality parameters. - Overseeing buying, merchandising, quality benchmarking, and market intelligence. - Managing vendor relationships, ensuring quality, availability, and negotiating prices. - Balancing product pricing and availability based on demand and seasonality. - Achieving targets related to sales, margin, promo negotiations, and stock planning. - Researching competitors for market understanding and suggesting pricing strategies. - Controlling inventory and ensuring timely product availability. - Developing pricing strategies to provide value to business units. Your work experience and skills should include: - Good communication skills. - Understanding of business dynamics. - Experience in Category Management and merchandising. - Subject Matter Expertise in specific product categories. - Experience in the Building material manufacturing sector. - Product marketing expertise including competitive analysis and trend forecasting. - Product life cycle management and catalog quality management. - Market analysis and achieving volume and profit goals. For this role, a Master's degree, preferably an MBA, is required. The salary range will be as per the company's policy, and the age limit is below 45 years.,

As a PCB Layout Engineer with 6-10 years of experience, you will be responsible for the following: - Good knowledge and skills in analog, digital, power, and mixed signal PCB designs. You should be well-versed in good layout practices such as cross talk, signal integrity, and controlled impedance. - Proficient in understanding electrical circuit functionality and electrical schematics. - Ability to work on complex designs and possess in-depth knowledge of Allegro PCB Designer tools. - Experience in working on multilayer PCB boards ranging from 8 to 16 layers. - Capable of routing boards with High-Speed interfaces (e.g., DDR, Giga-bit Ethernet), and meeting Signal Integrity and Controlled Impedance requirements. - Skilled in utilizing advanced tool features like design partitioning to manage workflow effectively. - Collaborate with hardware, mechanical, and manufacturing teams to identify design constraints and implement solutions. - Good working knowledge of SMT, BGA components, DFM, DFT, DFA, and IPC specifications. - Proficient in performing PC Board Layout of Complex Analog & Digital designs, creating Schematic & PCB package symbols, and managing the component library effectively. - Understand and implement best layout practices, Signal Integrity analysis, route Controlled Impedance Boards, and comply with DFM, DFT & DFA requirements. - Familiarity with Fabrication, Assembly & Manufacturing processes, IPC Standards, and EMI/EMC design practices. You will play a crucial role in ensuring high-quality PCB designs and collaborating effectively with cross-functional teams to deliver successful products.,

As an Investigation and Deviation Expert at Novartis, your primary responsibility will be to work collaboratively with process experts and multifunctional operations teams in Radio Ligand Therapy (RLT) platform sites. You will take ownership of deviation management for the site, actively participating in investigations of deviations, complaints, and OOXs. Your role will involve interacting with Cross-Functional Teams (CFT) and implementing Corrective and Preventive Actions (CAPA), Effectiveness Checks (EC), risk assessments, and quality management. Effective communication between teams and supporting problem-solving activities will be key in this role. Key Responsibilities: - Manage deviations in 1QEM system for the responsible sites using the Novartis quality management framework. - Conduct root cause analysis following established procedures and site practices. - Coordinate with various stakeholders from the Production unit, Quality Assurance, Engineering team, and site leadership team. - Ensure stakeholders are informed about the investigation progress, manage necessary communications, and adhere to timelines. - Participate in Deviation and RCI review meetings, capturing key information and translating it into actionable documentation. - Track and report on metrics related to change control documentation. - Develop, revise, and maintain high-quality documentation related to Deviation management processes. - Support quality management system (QMS) actions such as Change Controls, CAPA, risk assessments, and OOXs management. - Ensure inspection readiness for the area of responsibility. - Support the creation and review of GxP documents. - Assist with Health Authority (HA) audits and compliance with GxP environment. - Support implementation and adherence to safety and environmental protection requirements. - Comply with internal functional requirements and complete assigned tasks. Essential Requirements: - Quality / Accuracy / Right First Time - Timeliness - Deviations / Escalations - Quality System Management Support Specific Professional Competencies: - cGMP and Good Documentation Practices - Deviation Handling - Root Cause Analysis - Corrective Action and Preventive Action - Change Control Management - Knowledgeable on Effectiveness Checks - Continuous Process Improvement - Drug Substance Manufacturing - Process Design and Control - Complaints and OOXs Handling Education: - Bachelors degree in relevant science streams. M.Tech, M.Sc./M.S., or equivalent education is desirable. Languages: - Proficiency in English (oral and written). Experiences: - Minimum 12 years of experience in MS&T, Quality Assurance, Regulatory, or manufacturing of Biologics. - At least 5 years of experience in MS&T or Manufacturing operations. - Proficient knowledge of deviation handling, incident investigations, root cause analysis, and CAPA management. - Familiarity with regulatory guidance and statistical evaluations. In addition, Novartis is committed to diversity and inclusion, creating an outstanding, inclusive work environment. Joining the Novartis Network can help you stay connected and informed about career opportunities within the company. Novartis also offers a variety of benefits and rewards to support your personal and professional growth. As an Investigation and Deviation Expert at Novartis, your primary responsibility will be to work collaboratively with process experts and multifunctional operations teams in Radio Ligand Therapy (RLT) platform sites. You will take ownership of deviation management for the site, actively participating in investigations of deviations, complaints, and OOXs. Your role will involve interacting with Cross-Functional Teams (CFT) and implementing Corrective and Preventive Actions (CAPA), Effectiveness Checks (EC), risk assessments, and quality management. Effective communication between teams and supporting problem-solving activities will be key in this role. Key Responsibilities: - Manage deviations in 1QEM system for the responsible sites using the Novartis quality management framework. - Conduct root cause analysis following established procedures and site practices. - Coordinate with various stakeholders from the Production unit, Quality Assurance, Engineering team, and site leadership team. - Ensure stakeholders are informed about the investigation progress, manage necessary communications, and adhere to timelines. - Participate in Deviation and RCI review meetings, capturing key information and translating it into actionable documentation. - Track and report on metrics related to change control documentation. - Develop, revise, and maintain high-quality documentation related to Deviation management processes. - Support quality management system (QMS) actions such as Change Controls, CAPA, risk assessments, and OOXs management. - Ensure inspection readiness for the area of responsibility. - Support the creation and review of GxP documents. - Assist with Health Authority (HA) audi

As a DD&IT Senior Business Analyst RLT at Novartis, you will play a key role in shaping the future of RLT (radioligand therapy) manufacturing. Your responsibilities will include improving business processes, products, services, and software through data analysis and collaborative efforts. You will work closely with business leaders to identify requirements and provide data-driven solutions to enhance efficiency and add value. Operating as a liaison between business needs and IT solutions, you will drive global system deployments for improved operational efficiency and quality. Your tasks will involve leading integration efforts across MES, OT, and ERP platforms to ensure seamless rollouts and business continuity across multiple locations. Your work will adhere to legislation, internal rules, good practices, and business objectives. Key Responsibilities: - Perform data analysis, identify business needs, define requirements, document processes and procedures, and provide advice on enhancing efficiency. - Contribute to creating new models based on data-driven insights to improve efficiencies and add value. - Develop detailed business analyses, outline issues, identify gaps in existing functionality, recognize opportunities, and offer solution recommendations. - Create project or product rationale and conduct scoping assessments to assess feasibility. - Develop a comprehensive requirement specification to estimate costs, time, and resources for solution deployment. - Establish estimates and complete financial models, ensuring alignment with costs, savings, revenue opportunities, investment horizons, etc. - Ensure stakeholder involvement in specifying new or major upgrades to existing services or products. - Focus on user experience in designing new solutions and services, supporting super user training. - Ensure consistency and traceability between user requirements, functional specifications, and testing & validation processes. Qualification Required: - University diploma in Finance, IT, Business, or related fields. - Fluent in English (spoken and written). - Minimum 5 years of experience in the healthcare industry or relevant fields. - Experience in manufacturing IT/OT and ERP system integration. - Proven ability in leading functional and user acceptance testing. - Successful coordination of multi-site system rollouts. Desired Experience: - Familiarity with Manufacturing Execution Systems (MES) and Operational Technology (OT) platforms. - Experience in regulated or pharmaceutical manufacturing environments. The position offers permanent employment with a 6-month probation period. Applications should be submitted with a CV in Slovenian and English languages. In addition, Novartis is committed to diversity, inclusion, and providing accommodation to individuals with disabilities. For any necessary adjustments during the recruitment process or at the workplace, please contact diversity.inclusion_slo@novartis.com. Novartis values collaboration, support, and inspiration to develop breakthrough therapies that impact patients' lives positively. Join Novartis in creating a brighter future together. For further details on benefits and rewards, refer to: https://www.novartis.com/careers/benefits-rewards. Join the Novartis Network to explore career opportunities: https://talentnetwork.novartis.com/network. As a DD&IT Senior Business Analyst RLT at Novartis, you will play a key role in shaping the future of RLT (radioligand therapy) manufacturing. Your responsibilities will include improving business processes, products, services, and software through data analysis and collaborative efforts. You will work closely with business leaders to identify requirements and provide data-driven solutions to enhance efficiency and add value. Operating as a liaison between business needs and IT solutions, you will drive global system deployments for improved operational efficiency and quality. Your tasks will involve leading integration efforts across MES, OT, and ERP platforms to ensure seamless rollouts and business continuity across multiple locations. Your work will adhere to legislation, internal rules, good practices, and business objectives. Key Responsibilities: - Perform data analysis, identify business needs, define requirements, document processes and procedures, and provide advice on enhancing efficiency. - Contribute to creating new models based on data-driven insights to improve efficiencies and add value. - Develop detailed business analyses, outline issues, identify gaps in existing functionality, recognize opportunities, and offer solution recommendations. - Create project or product rationale and conduct scoping assessments to assess feasibility. - Develop a comprehensive requirement specification to estimate costs, time, and resources for solution deployment. - Establish estimates and complete financial models, ensuring alignment with costs, savings, revenue opportunities, investment horizons, etc. - Ensure

Role Overview: As an SAP Solution Architect / Functional Designer at Zoetis India Capability Center (ZICC) in Hyderabad, you will be instrumental in delivering SAP solutions that align with business requirements and best practices. Your primary responsibilities will include: Key Responsibilities: - Acting as an SAP Solution Architect / Functional Designer - Delivering SAP Solutions aligned with business requirements and best practices - Gathering requirements and estimating for SAP Project requests - Conducting thorough analysis to identify all potential impacts for project/enhancement requests - Designing, configuring, and testing SAP PP-PM solutions - Integrating QM interfaces with third-party applications - Designing, configuring, and testing SAP QM & Plant maintenance solutions - Providing project-related support for SAP PP-PI/MRP/MPS - Collaborating with peers in the ZTD organization and business representatives to determine business process and solution design leveraging the capabilities of the SAP modules and cross-modules integration - Coaching/Training others to bring them up to speed quickly and making them productive members of the functional team - Managing any colleagues and/or contractors reporting to this position - Providing support for global and regional systems and services - Working with Business counterparts to ensure audit, SOX, and other compliance requirements - Identifying and initiating process improvements (continuous improvement) - Monitoring process compliance and performance metrics Qualification Required: - Bachelor's degree in engineering, Computer Science, Manufacturing, Supply Chain, or a related field - Master's degree in business administration (MBA), Operations Management, or Manufacturing-related discipline preferred - At least 8 years of SAP delivery & configuration experience with multiple full life cycle implementations in the areas of SAP QM & PP-PM - Functional/technical proficiency with at least 3 full lifecycle SAP implementations and 2 years of industry (PP-PI/QM domain preferable) and/or consulting experience required Additional Company Details: Join Zoetis, the world leader in animal health, and be part of a culture that focuses on colleagues" careers, connection, and support. Your contributions will be valued as you help drive innovation and shape the future of animal healthcare.,

Role Overview: You will be responsible for developing advanced wearable infusion pump based drug delivery systems, integrating sensor & embedded systems, optimizing power management & miniaturization, designing user interface (UI), conducting testing & validation, collaborating cross-functionally, ensuring regulatory compliance, supporting manufacturing & scalability, managing documentation, vendor interactions, risk management, and product quality investigations. Additionally, you will drive program execution excellence while escalating urgent issues to leadership. Key Responsibilities: - Develop wearable infusion pump based drug delivery systems - Implement sensor & embedded systems integration - Optimize power management & miniaturization for portable use - Design user interface (UI) with clear visuals and intuitive features - Conduct testing & validation for device performance assessments - Collaborate cross-functionally with pharmaceutical teams and regulatory affairs specialists - Ensure regulatory compliance with relevant standards - Support manufacturing & scalability for commercial viability - Develop and maintain essential documentation - Manage vendor interactions for device suppliers, human factors, and visual design - Apply risk management for infusion pump development - Lead product quality investigations and corrective actions Qualifications: - Advanced degree in Mechanical Engineering, Electrical Engineering, Biomedical Engineering, or related technical discipline with 10+ years of industry experience - Demonstrated expertise in wearable injectors and continuous infusion pump development - Understanding of system thinking and human factors/usability engineering - Experience with device standards, quality management, and regulatory requirements - Strong analytical, problem-solving, and communication skills - Ability to work effectively in a multidisciplinary team environment,