Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. Your role is crucial in maintaining this commitment and driving forward our mission to improve patient outcomes. What You Will Achieve In this role, you will: Evaluate and review clinical and commercial drug batches to ensure quality. Ensure product and process documents meet established specifications through rigorous sampling and statistical process control. Identify and address deviations from manufacturing and packaging standards. Approve investigations and oversee change control activities to maintain compliance with configuration management policies. Contribute to project tasks and milestones, organizing work to meet deadlines. Learn and apply basic team effectiveness skills within the immediate work team. Make decisions within limited options to resolve basic problems under supervisor's direction. Ensure manufacturing and packaging records conform to Pfizer policy and cGMP standards. Maintain inspection readiness, support regulatory and customer inspections, and improve quality assurance systems. Assist manufacturing/packaging staff in real-time compliance error detection and resolution, and lead or participate in Quality Risk Management assessments. Here Is What You Need (Minimum Requirements) Bachelor's degree with any years of experience, or an Associate's degree with 4 years of relevant experience, or a high school diploma (or equivalent) and 6 years of relevant experience Experience in the pharmaceutical industry and Quality administered systems Sound knowledge of current Good Manufacturing Practices (part of GxP) Ability to work effectively in a team environment, both within one's own team and interdepartmental teams Effective written and oral communication skills Bonus Points If You Have (Preferred Requirements) Experience at a manufacturing site. Managing and writing deviations Experience in production batch record review, Enterprise Resource Planning system, investigation of non-conformance, root cause analysis and change control management Strong problem-solving skills Ability to work independently and as part of a team Excellent time management and multitasking abilities Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Quality Assurance and Control

Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. Your role is crucial in maintaining this commitment and driving forward our mission to improve patient outcomes. What You Will Achieve In this role, you will: Evaluate and review clinical and commercial drug batches to ensure quality. Ensure product and process documents meet established specifications through rigorous sampling and statistical process control. Identify and address deviations from manufacturing and packaging standards. Approve investigations and oversee change control activities to maintain compliance with configuration management policies. Contribute to project tasks and milestones, organizing work to meet deadlines. Learn and apply basic team effectiveness skills within the immediate work team. Make decisions within limited options to resolve basic problems under supervisor's direction. Ensure manufacturing and packaging records conform to Pfizer policy and cGMP standards. Maintain inspection readiness, support regulatory and customer inspections, and improve quality assurance systems. Assist manufacturing/packaging staff in real-time compliance error detection and resolution, and lead or participate in Quality Risk Management assessments. Here Is What You Need (Minimum Requirements) Bachelor's degree with any years of experience, or an Associate's degree with 4 years of relevant experience, or a high school diploma (or equivalent) and 6 years of relevant experience Experience in the pharmaceutical industry and Quality administered systems Sound knowledge of current Good Manufacturing Practices (part of GxP) Ability to work effectively in a team environment, both within one's own team and interdepartmental teams Effective written and oral communication skills Bonus Points If You Have (Preferred Requirements) Experience at a manufacturing site. Managing and writing deviations Experience in production batch record review, Enterprise Resource Planning system, investigation of non-conformance, root cause analysis and change control management Strong problem-solving skills Ability to work independently and as part of a team Excellent time management and multitasking abilities Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Quality Assurance and Control

Use Your Power for Purpose Our breakthroughs would not make it to the hands of patients without our dedicated and agile pharmaceutical manufacturing team. We rely on members who understand the importance and impact of their role in Pfizer’s mission. Patients need colleagues like you who take pride in their work and always strive to improve outcomes. You will help ensure that patients and physicians have the medicines they need when they need them. What You Will Achieve In this role, you will: Take responsibility for individual contributions to achieve team deliverables, working effectively as a team member and coordinating with others. Manage personal time and professional development, being accountable for results. Follow standard procedures to complete tasks of varying scope, sequence, and complexity within the agreed timeframe. Identify and solve moderately routine problems. Complete assignments with moderate supervision using established procedures, referring deviations from standard procedures to the supervisor. Ensure work is reviewed for accuracy, quality, and adherence to standards. Prepare and operate various components, materials, equipment, and machines in your assigned area, ensuring adequate inventory of parts and materials before starting a production run. Adhere strictly to all plant safety and current Good Manufacturing Practices (cGMP) regulations. Perform in-process quality inspections, and seek to implement process and safety improvements. Here Is What You Need (Minimum Requirements) High School Diploma or GED with 2+ years of relevant experience Strong analytical and problem-solving skills Excellent problem-solving and decision-making skills Excellent communication and interpersonal skills Ability to work independently and as part of a team Detail-oriented with strong organizational skills Bonus Points If You Have (Preferred Requirements) Previous experience in cGMPs (current Good Manufacturing Practices) environment Proficiency in using manufacturing software and tools Ability to adapt to changing priorities and work in a fast-paced environment Demonstrated leadership skills and ability to mentor team members Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Manufacturing

Use Your Power for Purpose Our breakthroughs would not make it to the hands of patients without our dedicated and agile pharmaceutical manufacturing team. We rely on members who understand the importance and impact of their role in Pfizer’s mission. Patients need colleagues like you who take pride in their work and always strive to improve outcomes. You will help ensure that patients and physicians have the medicines they need when they need them. What You Will Achieve In this role, you will: Take responsibility for individual contributions to achieve team deliverables, working effectively as a team member and coordinating with others. Manage personal time and professional development, being accountable for results. Follow standard procedures to complete tasks of varying scope, sequence, and complexity within the agreed timeframe. Identify and solve moderately routine problems. Complete assignments with moderate supervision using established procedures, referring deviations from standard procedures to the supervisor. Ensure work is reviewed for accuracy, quality, and adherence to standards. Prepare and operate various components, materials, equipment, and machines in your assigned area, ensuring adequate inventory of parts and materials before starting a production run. Adhere strictly to all plant safety and current Good Manufacturing Practices (cGMP) regulations. Perform in-process quality inspections, and seek to implement process and safety improvements. Here Is What You Need (Minimum Requirements) High School Diploma or GED with 2+ years of relevant experience Strong analytical and problem-solving skills Excellent problem-solving and decision-making skills Excellent communication and interpersonal skills Ability to work independently and as part of a team Detail-oriented with strong organizational skills Bonus Points If You Have (Preferred Requirements) Previous experience in cGMPs (current Good Manufacturing Practices) environment Proficiency in using manufacturing software and tools Ability to adapt to changing priorities and work in a fast-paced environment Demonstrated leadership skills and ability to mentor team members Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Manufacturing

Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. Your role is crucial in maintaining this commitment and driving forward our mission to improve patient outcomes. Role Summary: The MQ TS Downstream Associate is responsible for primary contact of quality on the floor, particularly in the Terminal sterilization, Visual Inspection and Packing areas of production and monitor processes for compliance to cGMP standards. Job Responsibilities: Responsible for ensuring operating state of cGMP compliance in Terminal Sterilization, Visual Inspection and Packaging operations. Maintain regulatory compliance in accordance with cGMP practices Ensure manufacturing policies and procedures conform to Pfizer standards Knowledge and hands on experience in reviewing eBR and assessing the impact of AMPs exceptions with technical support/inputs from Sr. Associate or Sr. Team Leader. Review of Batch reports and Equipment audit trails. Perform Acceptable Quality level sampling, Inspection in VIDT and Batch record review and release. Perform batch start-up and end activities viz. sensor challenge tests, recipe review etc. Perform random process checks for Terminal Sterilization, Visual Inspection and Packaging. Perform Daily walkthroughs and report observations to the Sr. Team Leader. Perform Equipment breakdown assessments w.r.t to Product Quality and patient safety with technical support/inputs from Sr. Associate or Sr. Team Leader. Review and assessment of equipment alarms and review of quarterly alarm trends. Report any non-compliance to the Sr. Associate or Sr. Team Leader. Should have trouble shooting abilities in manufacturing area, which helps the organization to develop, implement and achieve its mission, vision and values. Identify gaps and involve in Process and Procedure Simplification, thereby reduce downtime, and increase the Efficiency. Here Is What You Need (Minimum Requirements) B. Pharm any science degree 2-6 years of experience in Manufacturing Quality Assurance / Quality Assurance / Production of a pharmaceutical manufacturing facility. Experience in the pharmaceutical industry and Quality administered systems Sound knowledge of current Good Manufacturing Practices (part of GxP) Ability to work effectively in a team environment, both within one's own team and interdepartmental teams Effective written and oral communication skills. Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Quality Assurance and Control

Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. By being part of our team, you help uphold a quality culture that adapts and evolves to meet the needs of patients, ensuring that every product we deliver is of the highest standard. Your role is crucial in maintaining this commitment and driving forward our mission to improve patient outcomes. Role Summary: The MQ TS Downstream Associate is responsible for primary contact of quality on the floor, particularly in the Terminal sterilization, Visual Inspection and Packing areas of production and monitor processes for compliance to cGMP standards. Job Responsibilities: Responsible for ensuring operating state of cGMP compliance in Terminal Sterilization, Visual Inspection and Packaging operations. Maintain regulatory compliance in accordance with cGMP practices Ensure manufacturing policies and procedures conform to Pfizer standards Knowledge and hands on experience in reviewing eBR and assessing the impact of AMPs exceptions with technical support/inputs from Sr. Associate or Sr. Team Leader. Review of Batch reports and Equipment audit trails. Perform Acceptable Quality level sampling, Inspection in VIDT and Batch record review and release. Perform batch start-up and end activities viz. sensor challenge tests, recipe review etc. Perform random process checks for Terminal Sterilization, Visual Inspection and Packaging. Perform Daily walkthroughs and report observations to the Sr. Team Leader. Perform Equipment breakdown assessments w.r.t to Product Quality and patient safety with technical support/inputs from Sr. Associate or Sr. Team Leader. Review and assessment of equipment alarms and review of quarterly alarm trends. Report any non-compliance to the Sr. Associate or Sr. Team Leader. Should have trouble shooting abilities in manufacturing area, which helps the organization to develop, implement and achieve its mission, vision and values. Identify gaps and involve in Process and Procedure Simplification, thereby reduce downtime, and increase the Efficiency. Here Is What You Need (Minimum Requirements) B. Pharm any science degree 2-6 years of experience in Manufacturing Quality Assurance / Quality Assurance / Production of a pharmaceutical manufacturing facility. Experience in the pharmaceutical industry and Quality administered systems Sound knowledge of current Good Manufacturing Practices (part of GxP) Ability to work effectively in a team environment, both within one's own team and interdepartmental teams Effective written and oral communication skills. Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Quality Assurance and Control

Responsibilities: Responsible for primary contact of quality on the floor, particularly in the Visual Inspection Training, Terminal sterilization, Visual Inspection and Packing areas of production and monitor processes for compliance to cGMP standards. Responsible for ensuring operating state of cGMP compliance in Terminal Sterilization, Visual Inspection and Packaging operations Maintain regulatory compliance in accordance with cGMP practices Ensure manufacturing policies and procedures conform to Pfizer standards Knowledge and hands on experience in reviewing eBR and assessing the impact of AMPs exceptions with technical support/inputs from Sr. Associate or Sr. Team Leader Review of Batch reports and Equipment audit trails Perform Acceptable Quality level sampling, Inspection in VIDT and Batch record review and release Perform batch start-up and end activities viz. sensor challenge tests, recipe review, etc Perform random process checks for Terminal Sterilization, Visual Inspection and Packaging Perform Daily walkthroughs and report observations to the Sr. Team Leader. Perform Equipment breakdown assessments w.r.t to Product Quality and patient safety with technical support/inputs from Sr. Associate or Sr. Team Leader Review and assessment of equipment alarms and review of quarterly alarm trends Report any non-compliance to the Sr. Associate or Sr. Team Leader Trouble shooting in manufacturing area, which helps the organization develop, implement and achieve its mission, vision and values Identify gaps and involve in Process and Procedure Simplification, thereby reduce downtime, and increase the Efficiency Here Is What You Need (Minimum Requirements) BSC or B-Pharma / B-Tech with 5-7 years of experience Experience working in a Pharmaceutical Company Experience in the pharmaceutical industry and Quality administered systems Sound knowledge of current Good Manufacturing Practices (part of GxP) Ability to work effectively in a team environment, both within one's own team and interdepartmental teams Effective written and oral communication skills Bonus Points If You Have (Preferred Requirements) Experience at a manufacturing site. Managing and writing deviations Experience in production batch record review, Enterprise Resource Planning system, investigation of non-conformance, root cause analysis and change control management Strong problem-solving skills Ability to work independently and as part of a team Excellent time management and multitasking abilities Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Quality Assurance and Control

Use Your Power for Purpose Our manufacturing logistics and supply team ensures that customers and patients receive the medicines they need precisely when they need them. By embracing challenges, imagining new possibilities, and taking decisive action, you'll help accelerate the delivery of medicines to the world. Your role is crucial in making sure that life-saving treatments are available promptly, meeting the needs of patients everywhere. What You Will Achieve In this role, you will: Take responsibility for individual contributions to achieve team deliverables, working effectively as a team member and coordinating with others. Manage personal time and professional development, taking accountability for own results, and begin to prioritize own workflow. Follow standard procedures to complete tasks of varying scope, sequence, and complexity within the agreed timeframe, and assist in troubleshooting process issues. Share previously acquired knowledge to contribute to the success of the team and project, and ensure work is periodically reviewed with a focus on the soundness of technical judgment. Identify and solve moderately routine problems in a structured environment, making decisions that require choosing from limited options. Complete assignments with moderate supervision using established procedures and general instructions, referring deviations from standard procedures to the supervisor. Play a critical role in the movement of materials and finished goods within the plant, office, or warehouse, utilizing a variety of equipment such as forklifts, conveyors, cranes, hand carts, and power trucks. Assist in identifying required delivery and process improvements that drive increased efficiency, throughput, and quality, and make decisions on the best methods and procedures for different work situations. Adhere to all SOPs, current Good Manufacturing Practices (cGMPs), plant safety, quality, and documentation requirements, participate in audits, and ensure compliance with Corporate and Government Regulatory requirements for facilities and processes. Provide technical support to hi-rise operations, resolving issues and offering warehousing expertise, and complete necessary documentation using a computerized inventory system. Here Is What You Need (Minimum Requirements) High School Diploma or Graduate Science Degree with at least 2 years of experience. Handling of OEB- 4 & OEB-5 materials. Handling and operation of Isolator Handon experience in Raw materials dispensing Capable of completing documentation relative to the movement of inventory Demonstrated advanced knowledge of practices or concepts of Information Management and a working knowledge of practices, concepts and operations within other partner disciplines Ability to read, comprehend, and respond to verbal and written instructions/facility documents Ability to operate various types of motorized forklifts Proactive & effective communication within and across shifts Advanced electronic and computer skills including Excel, Word, Microsoft dynamics, Visio, SharePoint Bonus Points If You Have (Preferred Requirements) Experience in warehousing Handling of OEB- 4 & OEB-5 materials. Handling and operation of Isolator Handon experience in Raw materials dispensing Certification in the assigned area, if applicable Proactive and effective communication skills across shifts Warehousing experience Strong problem-solving skills Attention to detail and accuracy Ability to adapt to changing priorities and work environments Strong organizational skills Ability to handle multiple tasks simultaneously Work Location Assignment: On Premise Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Logistics & Supply Chain Mgmt

Use Your Power for Purpose The Maintenance Engineer plays a critical role in ensuring the reliability, compliance, and optimal performance of process equipment used in pharmaceutical manufacturing. This position involves leading maintenance strategies, troubleshooting complex equipment issues, and ensuring adherence to GMP (Good Manufacturing Practices) and regulatory standards. The role requires close collaboration with production, quality assurance, and engineering teams to support uninterrupted manufacturing operations and continuous improvement initiatives What You Will Achieve In this role, you will: Perform routine and preventive maintenance on Downstream areas: Sterilization, Visual Inspection, Packaging and Microbiology equipment. Troubleshooting of Major technical issues & handle Complex technical issues of: Sterilization, Visual Inspection, Packaging and Microbiology equipment. Lead and oversee preventive, predictive, and corrective maintenance activities for critical process equipment such as reactors, centrifuges, granulators, dryers, and tablet presses. Ensure all maintenance activities comply with GMP, FDA, and other regulatory requirements. Troubleshoot and resolve complex mechanical, electrical, and automation-related equipment issues. Develop and optimize maintenance SOPs, checklists, and documentation in alignment with quality standards. Coordinate with cross-functional teams during equipment qualification, validation, and change control processes. Analyze equipment performance data to identify trends, root causes of failures, and opportunities for reliability improvement. Manage spare parts inventory and vendor relationships for timely procurement and support. Mentor junior engineers and technicians, and lead training initiatives on equipment maintenance best practices. To perform FMEA & RCA and effectively trend equipment breakdowns and guide to implement corrective actions for improving reliability, here's a structured approach based on best practices in reliability engineering and maintenance management Calibrate instruments such as pressure gauges, temperature sensors, flow meters, and analytical instruments. Work with different types of PLCs, SCADA, and other PC based Automation systems used in pharmaceutical manufacturing. Support for automation projects and equipment upgrades Performing proactive maintenance activities to improve efficiency of downstream equipment. Here Is What You Need (Minimum Requirements) Qualification: Diploma or B. Tech in Instrumentation or Electronics Engineering. Experience: Diploma with 10-12 years industrial experience or B. Tech with 7-8 years industrial experience. Pharmaceutical Process Equipment Expertise In-depth knowledge of operation, maintenance, and troubleshooting of equipment. GMP & Regulatory Compliance Strong understanding of Good Manufacturing Practices (GMP), FDA, MHRA, and other regulatory requirements governing pharmaceutical manufacturing. Preventive & Predictive Maintenance Proficient in developing and executing preventive and predictive maintenance strategies to minimize downtime and extend equipment life. Root Cause Analysis (RCA) Skilled in conducting failure investigations and implementing corrective and preventive actions (CAPA) to address recurring equipment issues. Computerized Maintenance Management Systems (CMMS) Hands-on experience with CMMS platforms for scheduling, tracking, and documenting maintenance activities. Equipment Qualification & Validation Support Familiar with IQ/OQ/PQ protocols and supporting validation activities for new and existing equipment. Technical Documentation & SOP Development Ability to create and maintain detailed maintenance SOPs, equipment logs, and compliance documentation. Cross-Functional Collaboration Effective communication and coordination with production, quality assurance, engineering, and external vendors. Continuous Improvement & Reliability Engineering Focused on identifying opportunities for process and equipment optimization using tools like FMEA, TPM, and Six Sigma Bonus Points If You Have (Preferred Requirements) Asset Lifecycle Management Expertise in managing the full lifecycle of pharmaceutical equipment—from procurement and installation to decommissioning—ensuring cost-effectiveness and regulatory compliance. Regulatory Audit Readiness Proven ability to prepare for and support internal and external audits (e.g., FDA, MHRA, WHO), including documentation, walkthroughs, and corrective action implementation. Automation & Control Systems Advanced knowledge of PLCs, SCADA, and DCS systems used in pharmaceutical manufacturing, with the ability to troubleshoot and optimize automated processes. Risk-Based Maintenance Planning Application of risk assessment tools (e.g., FMEA, RCM) to prioritize maintenance activities based on criticality and impact on product quality and compliance. Data-Driven Decision Making Use of maintenance KPIs, OEE (Overall Equipment Effectiveness), and reliability metrics to drive continuous improvement and strategic planning. Change Management & Engineering Projects Leading equipment upgrades, retrofits, and technology transfers Certification in Maintenance or Reliability Engineering e.g., Certified Maintenance & Reliability Professional (CMRP), Certified Reliability Engineer (CRE), or equivalent. Knowledge of Validation Lifecycle Understanding of validation lifecycle documentation (URS, DQ, IQ, OQ, PQ) and its integration with maintenance activities. Project Management Skills Experience in managing maintenance-related capital projects, including budgeting, scheduling, and resource allocation. Exposure to Lean Manufacturing & Six Sigma Application of lean tools and Six Sigma methodologies to reduce waste, improve equipment uptime, and enhance process efficiency. SAP PM or Similar ERP Experience Hands-on experience with enterprise systems for maintenance planning, work order management, and asset tracking. Strong Documentation & Audit Trail Practices Ability to maintain accurate and audit-ready records in line with ALCOA+ principles (Attributable, Legible, Contemporaneous, Original, Accurate, and more). Training & Development Capabilities Experience in developing training modules and conducting technical training for maintenance teams. Work Location Assignment: On Premise Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Engineering

Qualifications Must-Have Graduate or Postgraduate in Pharmaceutical Science Discipline/Engineering. Minimum 8+ years of experience. Experience in manufacturing of pharmaceutical dosage forms (Sterile facility) Strong background and knowledge in manufacturing operations, compliance processes and systems. Experience and hand on electronic batch record design along with any associated software (i.e. FTPS (AMPS), SAP, MLM etc.) working exposure. Technical knowledge of manufacturing and packaging operations and operation process flow. Experience in defending process in regulatory audits /inspection. Preferably experiences in good understanding of manufacturing and quality systems. Effective communication skills are required, both written and verbal. Must be comfortable working both independently and collaboratively. Ability to communicate effectively with all cross functional teams (CFTs) within the organization. Nice-to-Have Master's degree Previous experience on SAP and Electronic batch record designing. (FTPS, PAS|X) Work Location Assignment: On Premise Work Location Assignment: On Premise Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Information & Business Tech

Strategic/ Policy Ensure achievement of Sales budgets for the assigned geographical territory Develop a clear understanding of his/her role as a responsible Officer of the Company and apply the knowledge, experience and skills to achieve the defined objectives for the position and the team. Review and discuss his/her plans for the achievement of territory’s sales budget each month (overall and product wise). Seek the assistance of the District Manager in formulating sales strategy. Conduct sales analytics to identify areas / stakeholders to be focused upon for driving business growth in the territory Provide inputs to the District Manager to help him validate the sales forecast or the rolling sales plan as per the defined frequency Provide inputs to the District Manager to help him manage salvage net to maintain it at an acceptable level Jointly with the District Manager, classify the medical practitioners in his/her territory in three categories A, B and C in the descending order of importance, A being the most important and C the least. Schedule the frequency of calls on the doctors depending on their criticality with respect to achievement of the sales targets for the district Deliver promotional messages tailored to each customer’s need so as to maximize sales Strictly adhere to coverage plans and frequency Strictly adhere to all applicable Pfizer policies and procedures. Operational / Process Regularly visit chemists in the area to ensure sale of Pfizer’s products, collect information on the sales of competitor’s products and regularly update the team about this data Stay updated on the competitors’ activities through personal visits to wholesalers and retailers. Maintain regularcontacts with medical practitioners, consultants, chemists and wholesalers. Book orders from the retailers to ensure adequate availability of products to meet the market demand. Also, ensure display of point-of-sale promotion material display in retailers’ stores in line with the promotion plan Ensure thorough pre-call planning and ask for the assistance of the District Manager wherever necessary. Prepare and implement special schedule for doctors’ visits/calls at the time of new product launch or sales campaign etc. using special presentation and promotional materials in line with the sales strategy Carry meticulous one-to-one detailing of the product bringing to the doctor’s attention the special features/benefits of the product, its proven efficacy, new research and clinical findings etc. Follow the approved tour program. Prepare and send daily reports as per the defined process on his/her day to day activities mentioning in detail about the calls made on the doctors clinics and hospitals. Maintain contacts with nursing homes, clinics and hospitals in his/her territory. Collect the data on annual budget for medicines with respect to each of the hospitals, their mode of purchase, rate contract, and drug committee members Forward adverse events and product complaints reported by customers and consumers in the appropriate format in a timely manner as described in the relevant SOPs Conduct taxi tours to meet the customers in micro-interiors and generate business for the products Conduct group meetings, speaker programs, and round table meetings for the doctors and chemists to create awareness around product benefits Build relationships with and manage Key Opinion Leaders (KOLs) and key customers Coordinate with CFA for inventory management Execute the product promotion campaigns for new and existing products for the territory Track the hospital purchase trend for the territory Conceive, plan and organize Continuing Medical Education (CME) programs with help from HODs, Consultants and hospital admin department People Trainee PSOs or other field trainees as may be assigned as mentees Share learning from experience with team colleagues Demonstrate and promote Pfizer global values in all interactions. Demonstrate team spirit and cooperation towards achievement of individual and team objectives Adhere to proposed training calendar for the year for self Act as the custodian of all compliance related matters for the territory Financial Ensure achievement of Sales budgets Assist in the collection of receivables, where required Ensure proper utilisation of product samples, detailing aids and other promotional material. Ensure proper accounting and reporting of expenses Technology Use technology solutions for enabling better information availability Use technology developments for effective field operations. Work Location Assignment:Flexible Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Sales

Use Your Power for Purpose Our breakthroughs would not reach patients without our dedicated pharmaceutical manufacturing team. We rely on agile members who understand the critical impact of their roles in Pfizer’s mission. Patients need colleagues like you who take pride in their work and continuously strive to improve outcomes. Your efforts ensure that patients and physicians have timely access to the medicines they need. The importance of your role cannot be overstated, as you help bridge the gap between innovation and patient care, making a tangible difference in countless lives. What You Will Achieve In this role, you will: Manage projects and set objectives within the Sub Business Unit, handling moderate complexity Lead people, technology, and financial resources, often through influence rather than direct authority Actively share knowledge and encourage others to do the same within the Sub Business Unit Identify and implement potential improvements in processes or products, taking risks to achieve results Solve complex problems, utilizing experience from various areas as needed Establish operational activities to support the Sub Business Unit's mid-term goals and recognize development needs Manage the performance of direct and indirect reports, aligning with the Sub Business Unit's objectives Partner with leadership from the Global or Sub Business Unit to achieve shared objectives Maximize quality and efficiency, complete batch records, and work in an integrated computerized manufacturing environment Train staff on safety practices, departmental procedures, product inspection, and Good Manufacturing Practices (GxP), while coordinating with other departments and supporting technical and engineering activities Here Is What You Need (Minimum Requirements) B.Pharm/M.Pharm/M.Sc/B.Sc with 10+ years of experience or Strong people management experience Effective written and oral communication skills Ability to communicate effectively within the department, cross-functionally at the site, and with outside customers and regulatory agencies Proficiency in computer literacy, particularly in managing Excel spreadsheets Knowledge of Microsoft Applications Bonus Points If You Have (Preferred Requirements): Master's degree Relevant experience in the pharmaceutical industry Strong background in Manufacturing, Technical Services, Materials Management, QA/QC, and Engineering Strong organizational and project management skills Excellent interpersonal and communication skills Ability to work collaboratively in a team environment Demonstrated ability to manage multiple priorities and projects Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Manufacturing

Use Your Power for Purpose Our breakthroughs would not reach the hands of patients without our dedicated pharmaceutical manufacturing team. We rely on agile members who understand the critical impact of their role in Pfizer’s mission. Patients need colleagues like you who take pride in their work and continuously strive to improve outcomes. Your efforts ensure that patients and physicians have timely access to the medicines they need. What You Will Achieve In this role, you will: Manage projects and set objectives, leading people, technology, and financial resources. Identify and develop innovative process or product improvements, taking calculated risks to achieve results. Solve complex problems, leveraging experience from various areas as needed. Manage the performance of direct and indirect reports, supporting team objectives and providing input to senior management. Partner with leadership to achieve objectives and manage teams, ensuring regulatory compliance and adherence to SOPs and cGMP requirements. Develop and manage a team of process technicians, optimizing facilities and equipment, and leading the implementation of Lean Tools. Support the development of SMART Objectives, participate in best practice sharing programs, and manage the performance and training of shift colleagues and contingent staff. Here Is What You Need (Minimum Requirements) High school diploma (or equivalent) with 8+ years of experience or associate’s degree with 6+ years of experience or BA/BS with 2+ years of experience or MBA/MS with any years of relevant experience Strong people management experience in a regulated manufacturing operations environment Excellent leadership, communication, and interpersonal skills A working knowledge of Upstream/Downstream Current Good Manufacturing Practices (cGMP) manufacturing operations Ability to work in a dynamic, fast-paced, and goal-driven environment Strong decision-making capability Bonus Points If You Have (Preferred Requirements) Relevant pharmaceutical industry experience Experience with Lean Tools and their implementation Excellent organizational and time management skills Ability to recognize development needs and create opportunities for colleagues Experience in maintaining regulatory compliance through established programs Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance Work Location Assignment: On Premise Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Manufacturing

The Global Commercial Analytics (GCA) team within the Chief Marketing Office (CMO) enables data-driven decision-making by translating complex analytics into intuitive, actionable insights for commercial leaders across brands and markets. A critical pillar of this mission is world-class data visualization and storytelling ensuring that advanced analytics are not only technically sound, but also clearly understood, trusted, and acted upon. As Senior Manager Data Visualization & Analytics Enablement , you will lead the visualization strategy for commercial analytics, owning the design, governance, and delivery of executive-ready dashboards and insight products . You will manage and develop a team of visualization specialists and BI developers, define visualization standards and best practices, and partner closely with Decision Analytics, Data Science, and Commercial stakeholders to ensure insights are communicated with clarity, consistency, and impact. This role is ideal for a leader who combines strong design judgment, deep BI expertise, and senior-level stakeholder management . Visualization Strategy & Standards Define and own the global visualization strategy for commercial analytics, including design principles, usability standards, and storytelling frameworks. Establish governance for KPI definitions, visual consistency, and user experience across dashboards and reports. Drive adoption of best practices in data visualization, accessibility, and executive storytelling. Dashboard & Insight Product Delivery Lead end-to-end delivery of executive and operational dashboards supporting field force effectiveness, commercial performance, ROI, and market insights. Ensure dashboards translate complex analytics into clear decisions, actions, and trade-offs. Balance flexibility for local markets with standardization at global and regional levels. Team Leadership & Capability Building Lead, coach, and develop a team of visualization developers and analytics translators. Review and elevate team output for quality, clarity, and business relevance. Build scalable templates, reusable assets, and visualization components to improve speed and consistency. Stakeholder Partnership & Enablement Partner with senior Commercial, Sales, Marketing, and Insights leaders to understand decision-making needs and tailor visual solutions accordingly. Act as a trusted advisor on how insights should be framed and communicated for executive audiences. Lead executive readouts and working sessions to drive adoption and action. Analytics & Data Platform Collaboration Work closely with Decision Analytics, Data Science, and Analytics Engineering teams to align visualization with underlying models and data pipelines. Ensure dashboards are built on trusted, governed data sources with appropriate performance, refresh cadence, and documentation. Influence tool strategy and roadmap across visualization platforms (e.g., Tableau, Power BI). Enablement & Change Management Drive user adoption through training, documentation, and enablement sessions. Champion data literacy and visualization best practices across the commercial analytics ecosystem. Continuously evaluate and incorporate new visualization techniques and platform capabilities. Basic Qualifications Bachelor's or Master's degree in Data Analytics, Information Design, Computer Science, Engineering, or a related field. 912 years of experience in Data Visualization, Business intelligence, or Analytics enablement roles. Demonstrated experience leading teams delivering enterprise-scale dashboards and reporting solutions. Deep expertise in Tableau and/or Power BI, including performance optimization and UX best practices. Strong working knowledge of SQL and data modelling concepts. Proven ability to translate analytical outputs into executive-ready visual narratives. Preferred/Good-to-Have Experience in pharmaceuticals, life sciences, or healthcare. Exposure to commercial analytics domains (sales performance, field force effectiveness, ROI). Familiarity with cloud data platforms (Snowflake, Databricks). Experience defining visualization governance and standards in global organizations. Professional Characteristics Visualization Strategist: Thinks beyond charts to decision journeys and executive narratives. People Leader: Builds, mentors, and inspires high-performing visualization teams. Executive Communicator: Able to influence senior stakeholders through clarity and design. Quality Champion: Holds a high bar for usability, accuracy, and consistency. Collaborative Partner: Works seamlessly across analytics, data engineering, and business teams. Change Leader: Drives adoption of analytics through better communication and enablement. Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Marketing and Market Research

Digital is helping Pfizer Global Supply win the digital race in pharma and create breakthroughs that change patients lives. Digital provides innovative digital solutions that unleash the power of our people by allowing them to focus their time and attention on value-add tasks. Our solutions accelerate key PGS initiatives and help PGS sites realize benefits of continuous improvement more rapidly. The Digital Manufacturing team enables a world-class manufacturing and supply chain organization by increasing visibility and efficiency across diverse systems and processes, and delivering predictive analytics and insights. The team supports Pfizer's Core Manufacturing & Engineering Solutions, while enabling a secure, seamless flow of contextualized data from the device & control levels, all the way to the top of the Enterprise. Our goal is to create persona driven, connected experiences across our shop floors to predict and optimize operations, while providing intelligence, and real-time insights to operators. Key?functional areas: Strategy & Operation Excellence Global Supply Engineering & Sustainment Manufacturing Operations Solutions E2E Network Solutions The NeoPLM Technical Delivery Lead is responsible for the technical leadership, coordination, and execution of NeoPLM platform deployments and enhancements across Pfizer's manufacturing network. This role ensures the successful delivery of NeoPLM solutions, driving standardisation, integration, and continuous improvement in product lifecycle management processes. The manager collaborates closely with site teams and cross-functional partners to enable successful deployment and ongoing optimisation of NeoPLM capabilities. Role Responsibilities The NeoPLM Technical Delivery Lead MOS's colleague's responsibilities include but are not limited to: Lead NeoPLM Technical Delivery: Oversee the end-to-end technical delivery of NeoPLM platform, ensuring robust architecture, integration, and compliance with Pfizer's digital standards. Develop and Execute Deployment Roadmaps: Create and manage detailed delivery plans for NeoPLM rollouts, upgrades, and enhancements, tailored to site and business requirements. Coordinate Pre-Deployment Readiness: Drive all preparation activitiesincluding stakeholder alignment, gap analysis, integration scoping, and process mappingto ensure sites are fully prepared for NeoPLM implementation. Facilitate Cross-Functional Stakeholder Engagement: Build trusted partnerships with site operations, quality, engineering, and automation teams to ensure shared ownership of the NeoPLM strategy, scope, and launch approach. Track Progress Against Milestones: Monitor and communicate progress against delivery milestones, escalating risks or blockers as needed. Governance & Reporting: Participate in delivery committees and bi-weekly reporting cadences to track progress, escalate issues, and refine strategy. Embed Delivery Accelerators: Contribute to and implement repeatable technical acceleratorssuch as playbooks, reusable templates, standard integration channels, and automation toolsto drive greater standardisation and programme acceleration. Manage Budget Inputs: Support financial planning for NeoPLM delivery by estimating costs, resource planning, and flagging potential variances to senior team members. Training & Enablement: Support onboarding andtraining efforts, and role-based access provisioning for NeoPLM users. Basic Qualifications BS in Engineering or Technology based subjects(s) or equivalent experience. 4+ years related work experience, 1-3 years of which would preferably be in a Global Solution environment focused on the build and deployment of Product Lifecycle Deployment (PLM). Relevant domain experience in manufacturing and/or quality operations. Experience in all stages of solution and application lifecycle from value analysis, business case development, and solution deployment through to value realization and system retirement is a significant advantage. Ability to work across multiple concurrent activities and successfully adapt to changing priorities as required. An understanding of system cGMP requirements and demonstrable knowledge of computer system design and maintenance lifecycle in cGMP environments. Preferred Qualifications Experience working with Neo PLM Experience with Agile Software Delivery as a Product Owner. Hands on experience in a manufacturing facility. Physical/Mental Requirements Ability to manage many parallel objectives and changing priorities. Understanding complex interrelationships between system components and design/implementation decisions. Non-standard Work Schedule, Travel Or Environment Requirements Due to the need to support global operations, the employee may be required to attend teleconference meetings that are outside of core work hours in IST. Ability to travel up to 25% Work Location Assignment: Hybrid Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Information & Business Tech

The Global Commercial Analytics (GCA) team within the Chief Marketing Office (CMO) organization is dedicated to transforming data into actionable intelligence, enabling the business to remain competitive and innovative in a data-driven world. We play a pivotal role in extracting insights from large and complex datasets to drive strategic decision-making. Collaborating closely with various subject matter experts across various fields, our team leverages advanced statistical analysis, machine learning techniques, and data visualization tools to uncover patterns, trends, and correlations within the data. Additionally, we are dedicated to delivering new, innovative capabilities by deploying cutting-edge Machine learning algorithms and artificial intelligence techniques to solve complex problems and create value. As a Senior Manager, Decision Analytics , you will lead teams delivering field force sizing, territory alignment, and commercial ROI analytics , while acting as a trusted thought partner to senior commercial, sales, and insights stakeholders. This role combines people leadership, technical depth, and strategic influence owning analytics delivery end-to-end, setting analytical direction, and ensuring insights are translated into clear recommendations that drive business action. You will coach and develop high-performing analytics teams, define best practices, and ensure analytical rigor, scalability, and consistency across markets. Analytics Strategy & Delivery Leadership Own and lead delivery of field force sizing, territory alignment, and commercial ROI programs across brands, markets, and therapeutic areas. Define analytical approaches, success metrics, and delivery roadmaps aligned to commercial strategy and business priorities. Ensure consistency, scalability, and methodological rigor across analytics initiatives. Team Leadership & Capability Building Lead, coach, and develop teams of analytics managers and individual contributors. Provide technical guidance on modelling approaches, data interpretation, and analytical trade-offs. Build reusable frameworks, standards, and best practices to improve efficiency and quality of analytics delivery. Field Force & Commercial Optimization Guide advanced modelling for rep sizing, deployment, coverage, reach, frequency, and workload optimization. Oversee complex scenario planning and simulations to evaluate strategic trade-offs and investment decisions. Ensure analytics outputs directly inform GTM strategy and execution. Commercial ROI & MMM Oversight Provide senior-level oversight and technical direction for pharma MMM (e.g., regression/Bayesian models, ad-stock, saturation, carryover). Translate MMM outputs into actionable budget allocation, ROI narratives, and investment recommendations. Partner with cross-functional teams to embed ROI thinking into planning and performance management. Stakeholder Management & Executive Storytelling Act as a trusted analytics advisor to senior Commercial, Sales, and Insights leaders. Lead executive-level discussions, clearly articulating insights, implications, and recommended actions. Manage competing stakeholder priorities and align analytics delivery to enterprise goals. Data, Platform & Architecture Collaboration Partner with Analytics Engineering, Data Science, and Platform teams to shape data architecture and pipelines that support advanced analytics. Ensure data quality, governance, and metric standardization across CRM, sales, claims, and market data sources. Drive adoption of scalable analytics tools and platforms (e.g., Dataiku, Snowflake, Databricks). Basic Qualifications Bachelor's or Master's degree in Data Science, Engineering, Economics, or a related quantitative field. 912 years of experience in commercial pharma analytics, sales/marketing analytics, or decision analytics. Demonstrated experience leading teams delivering complex analytics programs. Skills: Deep hands-on experience with field force analytics, territory alignment, GTM and commercial ROI / MMM. Strong technical foundation in SQL, Python, Tableau/Power BI, Excel, and PowerPoint (Executive Storytelling). Communication: Excellent verbal/written skills to elicit requirements, explain methodology, and present insights to senior business leaders. Experience with supporting commercial strategies and tactics, experience in pharmaceutical or healthcare industry is preferred. Preferred/Good-to-Have Experience operating in global, matrixed organizations. Exposure to advanced statistical modelling and machine learning techniques. Experience with cloud and big-data platforms (Snowflake, Databricks, Hadoop). Prior experience influencing senior commercial leadership or executive committees. PROFESSIONAL CHARACTERISTICS Strategic Analytics Leader: Connects advanced analytics to commercial strategy and enterprise outcomes. People Manager & Coach: Develops talent, builds high-performing teams, and fosters a culture of analytical excellence. Executive Communicator: Translates complex analytics into clear, compelling narratives for senior leaders. Delivery Owner: Balances rigor, speed, and pragmatism to drive results in ambiguous environments. Stakeholder Partner: Builds trust, manages expectations, and influences decisions without formal authority. Change Agent: Champions analytics-driven decision-making and continuous improvement. Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Marketing and Market Research

ROLE SUMMARY Do you want to make a global impact on patient health Do you thrive in a fast-paced environment that integrates scientific, clinical, and commercial domains through engineering, data science, and AI Join Pfizer Digital's Commercial Creation Center and CDI organization (C4) to leverage cutting-edge technology for critical business decisions and enhance customer experiences for colleagues, patients, and physicians. Our team of engineering, data science, and AI professionals is at the forefront of Pfizer's transformation into a digitally driven organization, using data science and AI to change patients lives. As the Director, Principal Engineer, AI and Data Engineering, you will be a leader within C4 team that leverages best practices from software engineering, data science, and analytics engineering to accelerate data-driven insight generation for the International Commercial business. In this role, you will be a technical advisor for developing and enhancing AI applications and integrating them into the enterprise analytics platform. You will help guide the strategic direction for AI within the International Commercial team while counseling business teams on how to evolve Pfizer International into a data-driven organization. In this process, you will work on diverse projects to close the loop between decisionmakers and data by leveraging software engineering best practices to develop applications with embedded AI. You will also integrate globally with Pfizer data science and AI teams to elevate AI assets to organizational or enterprise solutions for use at Pfizer. The ideal candidate is an expert in software engineering, data science, and AI with experience working in diverse and cross-functional teams, bridging the gap between data, technology, and people, to deliver the promise of AI to improve patients lives. Role Responsibilities Provide thought leadership in developing scalable AI solutions for Pfizer International Commercial model Design and lead the delivery of end-to-end data science and AI solutions including overseeing data ETL pipelines, server-side logic, ML engineering, frontend development, visualization, IaC, and CI/CD deployment Lead AI solutions development workstreams by providing expertise, thought leadership, and embodying best practices to drive technical and strategic objectives Lead discussions in cross functional forums to clarify model design, deployment, insights, and highlight implications to all cohorts of users Communicate complex technical concepts and insights to both technical and non-technical stakeholders to influence strategic decision-making Conduct advanced data analysis, predictive analytics, and design algorithms to solve business problems Mentor junior team members through technical and organizational leadership Research and apply new algorithms, technologies, and analytics practices to achieve business and technical objectives Build a sense of trust and rapport that creates a comfortable and effective workplace, and an ability to work as part of an agile team (product owner, developers, etc.) Represent the company in industry events and help recruit top talent Basic Qualifications 10+ years of work experience as a software engineer and tech lead for a diverse range of projects 5+ years of hands-on expertise in AI, data science, or software development 2+ years experience as a back-end or full-stack senior/staff/principal software engineer Computer Science, Engineering, Mathematics, or Statistics majors with data science or software development specialization Computer Science, Engineering, Analytics etc. Experience with the latest Large Language Models (LLM) public service API's (OpenAI & Claude), prompt engineering techniques, agentic framework (LangChain, Autogen, etc.) and serving concepts (MCP, A2A, etc.) Demonstrated experience interfacing with other internal and external teams to incorporate their innovations and vice versa Experience in developing and operating analytic workflows and model pipelines that are parametrized, automated and reusable Experience developing and deploying data and analytic products for use by technical and non-technical audiences Understanding of data science development lifecycle (CRISP) Strong hands-on skills in ML engineering and data science (e.g., Python, industrialized ETL software) Experience with test-driven development and automated testing frameworks (e.g. pytest, pydantic) Strong hands-on skills in CI/CD integration (e.g. GitHub, GitHub Actions or Jenkins) Strong hands-on skills in a cloud based analytics ecosystem (AWS, Snowflake, etc) Fierce curiosity, strong analytical skills, and strong sense of ownership in problem solving Strong verbal and written communication skills with Chinese and English language proficiency Preferred Qualifications Knowledge of business processes in commercial pharmaceutical domains would be strong plus Deep expertise with data science enabling technology, such as Dataiku Data Science Studio, AWS SageMaker, or other data science platforms Industry or consulting experience, along with project management skills strongly preferred Deep understanding of MLOps principles and tech stack (e.g. MLFlow) Experience in data ingestion, data warehousing, and data model concepts Strong hands-on skills for data pipeline orchestration (e.g. Airflow) Strong hands-on skills in containerization (e.g. AWS EKS, Kubernetes) Experience with big data technologies (e.g. Spark) Work Location Assignment: Hybrid Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Information & Business Tech

Use Your Power for Purpose Whether you are involved in the design and development of manufacturing processes for products or supporting maintenance and reliability, engineering is crucial to ensuring customers and patients receive the medicines they need, precisely when they need them. By collaborating with our forward-thinking engineering team, you'll play a key role in accelerating the delivery of medicines to the world. What You Will Achieve In this role, you will: Equipment Maintenance: Perform and oversee preventive and corrective maintenance of manufacturing equipment. Ensure timely calibration of instruments and compliance with standards. Utilities & Systems Management: Maintain HVAC systems, Purified Water systems, Environmental Monitoring systems. Troubleshoot SCADA and PLC systems to ensure smooth operations. Facility & Project Management: Manage facility maintenance activities and ensure readiness for audits. Support engineering projects from planning to execution within timelines and budgets. Compliance & Documentation: Prepare and maintain GMP documentation as per regulatory requirements. Ensure adherence to Quality Management System (QMS), CAPA, and Data Integrity principles. Safety & Risk Management: Implement industrial safety practices, fire and life safety measures. Conduct risk assessments and ensure compliance with EHS guidelines. Skills & Competencies: Strong knowledge of pharmaceutical manufacturing equipment and utilities. Expertise in preventive maintenance and troubleshooting. Familiarity with SCADA, PLC systems, and automation technologies. Good understanding of GMP, QMS, and regulatory compliance. Excellent project management and documentation skills. Strong commitment to safety and data integrity. Behavioral Attributes: Problem-solving and analytical skills. Ability to work under pressure and meet deadlines. Good communication and team collaboration skills. Here Is What You Need (Minimum Requirements) 6+ years of experience Demonstrated aptitude in basic mechanical, electrical, and instrumentation skills along with problem-solving techniques. A solid understanding of industry practices and standards, as well as basic mathematics. Familiarity with general trades such as construction, electrical, and machine shop work. Well-developed time management and problem-solving skills. Excellent communication skills. Experience with advanced diagnostic tools and techniques. Knowledge of regulatory requirements and compliance standards. Strong analytical and critical thinking skills. Excellent organizational and multitasking abilities. Project management Work Location Assignment: On Premise Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Engineering

Role Summary: The role of Associate package design and development will be Designing of Packaging commodities specifications, bill of material, artworks etc. Design of packaging process for required product-packaging configurations. Technical support on Packaging process to Production-packing and cross functional teams, troubleshoot exercise on packaging commodities and process. The associate packaging engineer is expected to develop packaging configurations and to manage technical efforts. Must be capable of ensuring resolution of all technical issues and providing timely implementation of all projects to maintain a consistent supply of our products to the market, while maintaining compliance to cGMPs. Create and provided Material codes, Key Line drawings and dimensions to Labeling team for the commercial artwork’s developments. Change control initiation and track the impact assessment, Pre-approval, and closure of change on time. Create Artworks request for Plant based changes, coordinate with Market coordinator and site supply chain team for LOCD, artwork center and accept PAR. Creates editors copy, operational copy of artworks, inputs to PAR per market and plant requirements. Review and approval of artworks for the printed packaging component. Preparation of packaging component specifications (Secondary and tertiary packaging component), and bill of materials, batch records, Preparation and approval of Shipper/case labels artwork, pallet label artwork, batch packing records, Standard test Procedure related to Packaging component and process. Review and approval of print proof & specimen of printed packaging component specifications. Serialization Support to production packing team. Technical support to production-packing Team for smooth launching of products. Work on commodity localization project for Primary and Secondary Packaging component. Preparation, review, and approval machine trial protocol for packaging components. Preparation, review, and approval of material evaluation protocol for packaging components. Review and approval of PPAP documents. Prepare Quality Risk assessment documents. Work with operation team and identify improvement projects and implement the same at site. IMEX for Packaging line as Process centric team. Cost improvement projects. Support to production packing team for new equipment’s/ machinery. Coordinate with cross functional team such as Pfizer site operations, Supply chain, Procurement, Engineering, Regulatory Affairs, Validation and Quality Assurance team for smooth executions of the project. Preferred Education/ Qualification: B.Sc/ M.Sc/ BE/ PGD in Packaging Technology (Preferable from Indian Institute of Packaging) Global Job Level J040 Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Engineering

Use Your Power for Purpose At Pfizer, technology impacts everything we do. Our digital and data first strategy focuses on implementing impactful and innovative technology solutions across all functions, from research to manufacturing. By digitizing drug discovery and development, identifying solutions, or making our work easier and faster, you will be making a difference to countless lives. Your dedication and hard work will be instrumental in helping Pfizer achieve new milestones and make a positive impact on patients worldwide. What You Will Achieve In this role, you will: Lead and guide moderately complex projects, effectively managing time and resources Apply skills and discipline knowledge to contribute to departmental work Make decisions to resolve moderately complex problems and develop new options in non-standard situations Work independently on assignments, seeking guidance on unusual or complex problems Utilize judgment and experience to become a resource for others and guide operational teams Facilitate agreements and collaboration between teams to ensure successful project delivery Act as a thought leader on emerging digital technologies, contributing to the vision, strategy, design, and roadmap of digital products Analyze support trends, lead process improvements, and evaluate data to understand user behavior and business trends Ensure project management deliverables comply with regulatory standards and maintain strong partnerships with Pfizer teams through effective engagement models Here Is What You Need (Minimum Requirements) BA/BS or MBA/MS with at least 5 years of relevant experience or PhD/JD with any years of experience Demonstrated experience of various Information Technology practices Experience with System Application and Products eDoc framework Familiarity with product analytics and strong ability to carry out analysis related to customer journey, user activity, product/feature performance, and other digital analytics Understanding of financial concepts and key success factors for business performance Knowledge of management reporting requirements and functional design Excellent communication skills Bonus Points If You Have (Preferred Requirements) Master's degree Relevant pharmaceutical industry experience Management consulting experience Experience with Agile Software Delivery and/or Scrum Master Certification Ability to mentor and guide other colleagues Strong collaboration and team facilitation skills Ability to analyze support trends and lead process improvements Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity. Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use Work Location Assignment: Hybrid Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Information & Business Tech