Urwah Admin

Pfizer

<div><div>Use Your Power for Purpose</div><div>
Are you ready to make your mark in a global organisation that values fresh ideas and bold thinking? Join Pfizer&rsquo;s Digital Colleague Services &amp; Adoption Team, where you&rsquo;ll help shape how thousands of colleagues experience technology every day.</div><div>
We&rsquo;re looking for a Senior Associate who&rsquo;s eager to learn, grow, and contribute to a team that&rsquo;s transforming digital support across regions. If you&rsquo;re passionate about solving problems, working with data, and exploring new technologies, this is your chance to build a meaningful career from day one. As a Senior Associate, you&rsquo;ll be at the heart of this transformation&mdash;championing service excellence, harnessing data-driven insights, and leveraging cutting-edge technologies to elevate the colleague experience.<br>
This isn&rsquo;t just about support, it&rsquo;s about empowering colleagues to do their best work. Your contributions will directly influence how thousands of Pfizer employees experience and interact with digital tools every day.<br>
You&rsquo;ll partner with passionate professionals across regions and disciplines. Together, you&rsquo;ll build a workplace that&rsquo;s smarter, faster, and more human-centric.</div><div></div><div><br>
What You Will Achieve</div><div>
In this role, you will:</div><ul><li>
Conduct proactive analysis of service data to uncover trends and opportunities for improvement.</li><li>
Identify service risks and plan mitigation with Service Owners</li><li>
Develop dashboards and reports using Power BI and other tools to support decision-making and performance tracking.</li><li>
Design and implement automation workflows using Power Automate to streamline repetitive tasks and improve service efficiency.</li><li>
Apply knowledge of agentic agents and AI frameworks to deliver intelligent solutions to continuously enhance service operations.</li><li>
Partner with stakeholders to identify and enable predictive triggers and self-service enhancements.</li><li>
Collaborate with global and regional teams to align service strategies and share best practices.</li><li>
Manipulate complex data sets to unlock opportunities for improvement, reduce friction and enhance productivity.</li><li>
Effectively communicate technical issues/challenges to non-technical people.</li></ul><div></div><div>
Here Is What You Need (Minimum Requirements)</div><ul><li>
Bachelor&rsquo;s Degree</li><li>
2+ years experience in an IT related field with knowledge of supporting end users with technical issues.</li><li>
Experience in data analytics, preferably within a service or operations context.</li><li>
Proficiency in Power Automate and Power BI.</li><li>
Experience using Copilot</li><li>
Strong communication and stakeholder management skills.</li><li>
Ability to work independently and manage multiple priorities in a fast-paced setting.</li><li>
Awareness of internal and external technology trends.</li><li>
Must be self-motivated, must have an ability to work well in a geographically dispersed, virtual team environment, and must exhibit a positive and professional attitude</li></ul><div></div><div>
Bonus Points If You Have (Preferred Requirements)</div><ul><li>
Preferred exposure to AI/ML concepts and their application in enterprise service contexts.</li><li>
Project Management skills</li><li>
Understanding of agentic agents and AI solution delivery in enterprise environments.</li><li>
Certification in Power Platform (Power BI, Power Automate).</li><li>
Experience working with Service Now framework</li></ul><div></div><div>
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS</div><div>
This is a hybrid role requiring a minimum of 3 days per week in the office. Ability to work a variety of hours as the role is part of a global team with stakeholders working different time zones.</div>
<br>
Work Location Assignment: Hybrid<div></div><div><br>
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</div><div></div>
Information &amp; Business Tech</div><div></div>

Sr. Associate Data & Analytics

<div></div><div><div>ROLE SUMMARY</div><div>
As part of the Clinical Data Sciences group, an integral delivery unit within the Clinical Development &amp; Operations (CD&amp;O) organization, the Senior Central Testing Analyst is responsible for leading the Database Testing and validation activity at a study or asset level and performing testing of database (UAT) and ensuring that the CRFs are designed in accordance to protocol and the end users are able to enter the data as per the standards and expectation. In addition to the screen testing the Senior Central Testing Analyst will also be responsible to perform the testing of data specification to ensure that the checks are rightly programmed, appropriate and adequate as per the protocol requirement.</div><div></div><div>
ROLE RESPONSIBILITIES</div><ul><li>
Provides technical skills and knowledge to assigned work to achieve and perform activities, including but not limited to: the testing of CRF design, Database building, Acquisition &amp; Processing of electronic data, such as external eData, Lab Data and PK/PD Data; Data extraction and listing for quality review, Data Visualization; Data and Documentation Processing, CRF and Database edit checks/validation and outputs.</li><li>
Accountable for high quality and on time delivery for assigned deliverables.</li><li>
Participate in initial DM meetings with Clinical Data Scientist (CDS) to understand the expectation and scope of the study.</li><li>
Ensure work carried out in accordance with applicable SOPs and working practices.</li><li>
Understand the Protocol and provide input to Study Team on Database Design and Edit Check Specification as appropriate.</li><li>
Based on Study Data Specification (SDS) the Screen UAT has to be executed and compare the Schedule of Assessment from Protocol with Database and Provide Suggestions.</li><li>
Review the Edit Check Specification, write UAT test scripts.</li><li>
Execute the scripts and log the issues in UAT tracker and provide feedback to Study Team</li><li>
May perform peer review on programming of edit checks</li><li>
May perform check on metadata listing</li><li>
Participate in UAT feedback meetings</li><li>
Streamline/Standardize the Scripts for Standard Forms/Edit Checks</li><li>
Validation of Manual queries/Listings (Standards/Therapeutic Specific)</li><li>
Able to understand the Postproduction Changes in Database during conduct and provide clinical/technical suggestion.</li><li>
Communicates effectively to study team about suggestion and changes to database.</li><li>
Track the lessons learned and share the knowledge across the team.</li><li>
Complete all the documentation related to study and share it with study team.</li><li>
Perform testing of reports and document the same.</li><li>
Maintain a high customer satisfaction level and work with global study teams to meet objectives/timelines.</li><li>
Able to resolve conflicts, influence and communicate with key stakeholders and customers.</li><li>
Organizes own work to time to meet agreed milestones and targets; develops plans for short-term work activities on own assignments (timelines, work plans, deliverables).</li><li>
Learns and applies basic team effectiveness skills (e.g., commitment, feedback, consensus management).</li></ul><div>
QUALIFICATIONS</div><ul><li>
Demonstrated knowledge of clinical development process including knowledge and understanding of the principles of GCP</li><li>
Demonstrated knowledge of data management processes and principles in area of responsibility.</li><li>
Working knowledge of all phases of clinical trials and ability to assess and determine study requirement from protocol review</li><li>
Demonstrates strong verbal and written communication skills including ability to communicate remotely</li><li>
Minimum 7 years of relevant experience required</li><li>
Working knowledge of clinical research, FDA &amp; ICH, GCP, GCDMP, and related regulatory requirements</li><li>
Proficient experience using commercial clinical data management systems and/or EDC products (e.g., Inform preferred)</li><li>
Experience using data visualization tools (e.g. Spotfire, J-Review) preferred</li><li>
Familiarity with MedDRA/WHO-Drug</li><li>
Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.)</li><li>
Bachelor&rsquo;s degree minimum requirement.</li><li>
Experience of project management skill in terms of resource management and timeline and quality control preferred.</li><li>
Experience performing testing of database and/or leading a team of testers performing the UAT activities.</li></ul>
<br>
Work Location Assignment: Hybrid<div></div><div><br>
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</div><div></div>
Medical</div><div></div>

Senior Associate, Senior Central Testing Analyst

<div><div>Summary</div><ul><li>
An Individual Contributor role</li><li>
Productive hands on programming, supporting deliverables in the study/project/portfolio/standards team, of medium &ndash; high complex statistical programming deliverables to support assets and study teams</li><li>
Performs tasks with limited supervision early in role and independently later in role.</li><li>
Is capable of handling standards/study programming specific activities independently including collaboration across stakeholders at various timezones</li><li>
Ensures adherence to high quality programming standards in their daily work</li><li>
Ensure the tasks are completed on time with quality and are compliant to the process at Pfizer with needed guidance.</li><li>
Work collaboratively with study teams and stakeholders such as clinicians and statisticians on milestones and deliverables.</li><li>
Active self-learning and delivering on solutions in the space of statistical programming and data standards</li><li>
Contribute to SDSA initiatives globally and locally.</li></ul><div></div><div>
Job Responsibilities :</div><ul><li>
Accountable for their assigned work supporting the standards/study deliverables</li><li>
Contributes to upto 80% of their time to programming deliverables assigned within the scope of the function in either SAS, R or Python and 20% to self learning, development and growth.</li><li>
Review/Develop/Validate datasets, TFL as per CDISC aligned Pfizer Standards or Pfizer Data Standards for Study/Project/Portfolio (TA or Study Programming)</li><li>
Explore the existing code base and execute/perform runs as required, also develop/modify as per the needs and specifications suggested to the standards team as appropriate &ndash; (Standards Programming)</li><li>
Ensures appropriate documentation and QC across the lifespan of the study for all of their programming deliverables across Standards, Programming and Submissions.</li><li>
Understand/Develop/Review standard/study/project/portfolio requirements, specifications to gain deeper understanding of expectations and programming requirements, by collaborating with stakeholders.</li><li>
Knowledgeable in core safety standards as well as TA standards pertinent to their project and lead development of standards necessary for their study</li><li>
Exhibits routine and occasionally complex problem solving skills, seeking direction when appropriate.</li><li>
Regularly update leads on progress and time estimations to ensure smooth daily operations and accurate planning</li><li>
Advances job knowledge to next level by participating/contributing in/to opportunities both globally and locally.</li></ul><div><br>
<br>
Work Location Assignment: Hybrid</div><div></div><div><br>
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</div><div></div>
Medical</div><div></div>

Senior Associate, Senior Statistical Data Scientist

<div><div>ROLE SUMMARY</div><div>
Digital is helping Pfizer Global Supply win the digital race in pharma and create breakthroughs that change patients&rsquo; 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.</div><div>
The Manufacturing Technology &amp; Solutions 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&rsquo;s Core Manufacturing &amp; Engineering Solutions, while enabling a secure, seamless flow of contextualized data from the device &amp; 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:</div><ul><li>
Strategy &amp; Operation Excellence</li><li>
Global Supply Engineering &amp; Sustainment</li><li>
Manufacturing Operations Solutions</li><li>
E2E Network Solutions</li></ul><div>
The Senior Associate, Manufacturing Operations Solutions colleague will support the deployment of solutions that drive operational discipline with a focus on increasing process robustness, yield improvements &amp; product quality, while increasing asset utilization and manufacturing attainment (e.g. Manufacturing Execution Solutions, MES). An ideal candidate will have a technical background with business process understanding across Manufacturing. The candidate will support the deployment and delivery of Electronic Batch Records (EBRs) and accelerators to Digital Industry 4.0 maturity.</div><div></div><div>
ROLE RESPONSIBILITIES</div><div>
The Senior Associate, Manufacturing Operations Solutions colleague&rsquo;s responsibilities may include, but are not limited to:</div><div></div><ul><li>
Support the design and deployment of site-wide MES solutions under the guidance of senior team members.</li><li>
Participate in project teams to help scope, plan, and execute solution deployments.</li><li>
Participate in process mapping and requirements gathering activities.</li><li>
Help define and build Electronic Batch Record template designs</li><li>
Help define and deliver accelerators to MES deployment, including AI.</li><li>
Help troubleshoot technical issues related to MES recipes and solution development, escalating as needed.</li><li>
Collaborate with senior team members to define next-level vision of business solutions for PGS.</li><li>
Collaborate with cross-functional teams (manufacturing, automation, QA, solution engineering etc.) to support project objectives.</li><li>
Assist with collecting and analysing data to support performance metrics and process improvement initiatives.</li><li>
Assist with documentation, including user and functional requirements, software configuration, and system maintenance records.</li></ul><div></div><div>
BASIC QUALIFICATIONS</div><ul><li>
BS in Engineering or Technology based subjects(s) or equivalent experience.</li><li>
3+ years related work experience.</li><li>
Relevant domain experience in manufacturing and/or quality operations.</li><li>
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.</li><li>
Ability to work across multiple concurrent activities and successfully adapt to changing priorities as required.</li><li>
An understanding of system cGMP requirements and demonstrable knowledge of computer system design and maintenance lifecycle in cGMP environments.</li></ul><div></div><div>
PREFERRED QUALIFICATIONS</div><ul><li>
1-3 years&rsquo; experience in a Global Solution environment focused on the build and deployment of Manufacturing Execution Solutions (MES).</li><li>
Experience working with Rockwell Pharmasuite or Siemens OpCenter Execution Pharma.</li><li>
Experience with Agile Software Delivery.</li><li>
Hands on experience in a manufacturing facility.</li></ul><div></div><div>
PHYSICAL/MENTAL REQUIREMENTS</div><ul><li>
None</li></ul><div></div><div>
NON-STANDARD WORK SCHEDULE, TRAVEL OR ENVIRONMENT REQUIREMENTS</div><div>
Ability to travel up to 25% and may on infrequent occasions be required to support weekend or night solution issue resolution, cutover and/or upgrade activities.</div><div>
Team is EU &amp; US based &ndash; work hours may be required to be adjusted accordingly.</div><br>
<div></div>
<br>
Work Location Assignment: Hybrid<div></div><div><br>
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</div><div></div>
Information &amp; Business Tech</div><div></div>

Senior Associate, Manufacturing Operations Solutions

<div><div><i>Identifying Job Information</i></div><div>
JOB TITLE:</div><div>
RIO Execution Hub Associate</div><div></div><div>
JOB INFORMATION</div><div>
JOB SUMMARY</div><div>
Summarize the primary purpose &amp; key accountabilities of the job.</div><div>
The RIO Execution Hub Associate is responsible for providing regulatory support to the International country and/or cluster Regulatory teams.</div><div></div><div>
The Execution Hub Associates work across portfolio phases from initial registration applications, lifecycle management through to product withdrawal. They support numerous regulatory activities that include but are not limited to;</div><ul><li>
M1 dossier components (local document authoring and/or coordination)</li><li>
Simple local only HA query responses,</li><li>
Provide support for general x-functional activities to country Regulatory teams for tenders, out-of-stock reporting, Annual Product Quality Review, risk minimization plans, and coordination of regulatory input for launch planning.</li></ul><div></div><div>
It is expected that this role partners closely with the Country Regulatory Strategist and Hub Submission/Dossier Managers to enable timely, high-quality submissions and sustained compliance. This includes but is not limited to:</div><ul><li>
Identification of regulatory requirements (for the in-scope submission categories defined),</li><li>
Authoring, delivery and/or coordination of local, submission-ready documents and</li><li>
The quality review/approval of the Dossier provided by Hub Submission/Dossier Managers (for the in-scope submission categories defined).</li></ul><div></div><div>
JOB RESPONSIBILITIES</div><div>
Indicate the primary responsibilities critical to the job.</div><div>
RIO Execution Hub Associate is focused on end-to-end management of multi-regional, regional and national regulatory dossiers for assigned cluster/country/therapeutic area/products, both initial registration applications and ongoing lifecycle management through to product withdrawal. Associated functions are engaged to provide smooth operational performance and process efficiency.</div><div></div><div>
This role executes the GRS mission by delivering against goals, executing initiatives, implementing new opportunities, and filling gaps related to the production of regulatory International and operational support. A key component of this role is the implementation of portfolio execution efficiencies, identification and escalation of quality and compliance issues or emerging risks detected during the management of the Cluster/Country submissions under his/her responsibility.</div><div>
Success in this role is measured by the timeliness, quality, compliance, and efficient delivery of critical on-the-job deliverables, bringing efficiencies to the organization.</div><div></div><div>
In some regions/clusters, the RIO Execution Hub can execute the role of Hub Submission Manager, while in others should closely partner with Hub Submission Manager.</div><div></div><div>
Key Accountabilities include:</div><div>
General accountabilities (For reference only)</div><ul><li>
Ensure timely delivery of local M1 dossier components</li><li>
Perform Quality review/approval of the Dossier build Table of Contents provided by Hub Submission/Dossier Managers (for the in-scope submissions under his/her responsibility).</li><li>
Can provide support for simple tenders, out-of-stock reporting, Annual Product Quality Review, risk minimization plans, and regulatory information status for launch planning.</li><li>
Provide support for local audit readiness activities, Dear Healthcare Professional Communication (DHPC) responses, and responses to medical info requests as requested</li><li>
Parther with Grow submission managers and Regional Submission Hubs to meet growth application delivery in line with International Commercial knots prioritisation and OP plans.</li><li>
Partner with Submission Hubs to meet GRS lifecycle prioritisation for CMC and Labelling changes.</li></ul><div>
Local document authoring &amp; submission prep (For reference only)</div><ul><li>
Author and review of M1 local documents (cover letters, variations, MA applications), and relevant translations.</li><li>
May engage with Labeling Hubs and clusters/countries on Labels and Artwork updates to include local requirements, ensuring alignment with approved text and supporting launch activities.</li><li>
Support clusters/countries with authoring of simple HA query responses e.g., admin related requests, and coordinate with relevant SMEs/functions (e.g., CMC) to address more complex HA queries, based on CRS query response strategy.</li></ul><div></div><div>
Portfolio &ndash; Non Portfolio Support (qualitative examples)</div><div>
Associate</div><div>
Business Experiences:</div><ul><li>
Provides regulatory support to lower complexity regulatory activities in the assigned country/Cluster (mainly for commercial lifecycle through to product withdrawal) and applies technical experience to impact business results.</li></ul><div>
Non-Portfolio Experiences:</div><ul><li>
Provides input to projects requested within RIO Hubs</li></ul><div></div><div>
QUALIFICATIONS / SKILLS</div><div>
Indicate qualifications and skills that are necessary for performance of responsibilities including: education, relevant experience, licenses, certifications and other job-related technical and managerial skills.</div><ul><li>
B.S./B.Scs. is in Pharmacy, Life Sciences, Business or Information Technology (desirable); equivalent relevant professional experience will be considered.</li><li>
Advanced to Fluent English language required. Multilingual skills desirable.</li><li>
Proven technical aptitude and ability to quickly learn and use new software, regulations and quality standards.</li><li>
Advanced Microsoft Office Suite skills.</li><li>
Familiarity with pharmaceutical organizational structures, systems, and culture is preferred.</li><li>
An understanding of country/cluster regulatory requirements and trends is preferred.</li><li>
Relevant experience within pharma, in Regulatory, quality and/or compliance fields preferred.</li></ul><div></div><div>
Working habits (qualitative examples)</div><div>
Associate</div><ul><li>
Colleague who requires management oversight on daily work and support in problem solving.</li><li>
Demonstrates technical expertise which aids in task-based execution.</li></ul><div></div><div>
ORGANIZATIONAL RELATIONSHIPS</div><div>
Provide the primary groups or key role(s) that this role will have interaction with as a regular part of the Job responsibilities. Include any external interactions as appropriate.</div><div>
RIO Execution Hub Associate/Sr Associate interacts with</div><ul><li>
Country/Cluster teams, Submission Manager hubs and other functions across RIO</li><li>
GIPE</li><li>
RIO Execution Hub Associate/Sr Associate can interact with Local affiliate cross functional teams for BAU well defined and simple M1 local components (e.g. Medical, Safety, Clinical, DRSD). informing or via the Country Regulatory team per agreements established</li></ul>
<br>
Work Location Assignment: On Premise<div></div><div><br>
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</div><div></div>
Regulatory Affairs</div><div></div>

RIO Execution Hub Associate

<div><div>Pfizer is committed to delivering high-quality, safe, and effective products to those who need them most. Within our Digital division, we foster a science-driven, risk-aware quality culture that supports our mission to improve patient outcomes through innovation and technology.</div><div></div><div>
We are seeking a Data Scientist to join the SAP Analytics Enablement (SAE) team. This team is responsible for developing SAP-based operational analytics and machine learning solutions that drive digital transformation across the enterprise.</div><div></div><div>
As a Data Scientist and Advanced Analytics Solution Developer, you will play a critical role in designing and delivering analytical products that address complex business challenges.</div><div></div><div>
Key Responsibilities</div><ul><li>
Collaborate with business and creation center SMEs to understand customer needs and deliver actionable, model-driven solutions.</li><li>
Lead the full machine learning lifecycle: research, design, experimentation, development, deployment, monitoring, and maintenance.</li><li>
Analyze large, complex datasets to extract meaningful insights and support decision-making.</li><li>
Develop prototypes and implement AI/ML algorithms in collaboration with data product owners, engineering teams, and business users.</li><li>
Optimize model performance through hyperparameter tuning and model selection.</li><li>
Continuously enhance models to better align with evolving business needs.</li><li>
Partner with support and operations teams to deploy new and updated analytical solutions.</li></ul><div></div><div>
Strategic Impact</div><div>
This role is central to advancing SAE&rsquo;s AI, Data &amp; Analytics strategy by:</div><ul><li>
Partnering with high-performing teams across the enterprise</li><li>
Supporting research and innovation initiatives</li><li>
Identifying and applying emerging technology trends</li><li>
Driving measurable value for internal and external stakeholders</li></ul><div></div><div>
ROLE &amp; RESPONSIBILITIES</div><ul><li>
Drive the development and enhancement of Pfizer&rsquo;s SAP Analytics systems, leading hands-on initiatives to deliver cutting-edge digital solutions and fostering innovation throughout the application lifecycle</li><li>
Define and set objectives for the vendor application team&rsquo;s operations, prioritizing resources and planning/deploying solution deliverables to support business requirements</li><li>
Provide technical and application knowledge leadership to the members of the vendor application development team, leveraging technical and functional expertise across multiple disciplines</li><li>
Partner with support and operations teams to share knowledge of Pfizer&rsquo;s new technologies and processes; both to define and implement support requirements and to manage the transition of products and solutions to long-term operations support.</li><li>
Take well-managed risks while ensuring the highest level of quality and compliance related to software development, enhancements, documentation and change management</li></ul><div>
BASIC QUALIFICATIONS</div><ul><li>
Bachelor&rsquo;s degree or higher in technical discipline (computer science, engineering, etc.)</li><li>
4+ years (2+ years with MBA/MS) of experience in information technology, analytics, or related field</li><li>
Experience in regression modeling, machine learning, natural language processing, data analysis, application of distributed systems to scale solutions, linear algebra, calculus</li><li>
Experience in Linear Algebra, Probability &amp; Statistics, Multivariate Calculus; programming with SQL, Python</li><li>
Experience in supervised and unsupervised Machine Learning algorithms and deep learning frameworks; Data Visualization; data wrangling, developing pipelines for Machine Learning</li><li>
Experience with building big data pipelines and Data Manipulation /data analytics / data management / Big data system.</li><li>
Industry experience with writing code (e.g., Python, Pytorch, PyScala, PySpark, JavaScript) and taking ML models/ algorithms to production</li><li>
Strong analytical skills, results-oriented, customer-oriented attitude, good strategic and conceptual thinking skills</li><li>
Ability to present complex information in a clear and concise manner.</li></ul><div>
PREFERRED QUALIFICATIONS</div><ul><li>
Pharmaceutical industry experience</li><li>
Knowledge of SAP BDC including Datasphere and Databricks</li><li>
Design Replication Flows in Datasphere .</li><li>
Develop and maintain Spaces, Local Tables, Views, Data Flow, Replication Flow, Transformation Flow, DAC, Task Chain, and Intelligent Lookup within SAP Datasphere</li></ul><br>
<div></div>
<br>
Work Location Assignment: Hybrid<div></div><div><br>
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</div><div></div>
Information &amp; Business Tech</div><div></div>

Manager, SAP Data Scientist

<div><div>Use Your Power for Purpose</div><div>
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 when they need them. By collaborating with our forward-thinking engineering team, you'll contribute to delivering medicines to the world more swiftly by envisioning new possibilities and taking decisive action. Your technical skills will be crucial in ensuring our plants, utility systems, buildings, and equipment are operational. Pfizer depends on you for the maintenance, redesign, and repair of utilities in our facilities, including electrical, plumbing, carpentry, air conditioning, heating, painting, and general upkeep. You will be responsible for taking preventive and corrective actions, setting priorities, forecasting, and allocating resources for maintenance tasks. Your dedication and focus will enable Pfizer to reach new milestones and support patients worldwide.</div><div></div><div>
What You Will Achieve</div><div></div><div>
The Incumbent as a member of Engineering team is second in command in the department and is responsible for providing engineering and maintenance support in compliance with Plant SOPs, cGMP, Good engineering Practices, EHS and Global Engineering standards, Budgets, in the assigned areas. Is responsible for ensuring continuous availability of machines for Production, monitoring other required parameters.</div><div>
In this role, you will:</div><ul><li>
Lead and manage people, technology, and financial resources within the department.</li><li>
Actively share knowledge and identify potential improvements in processes or products, taking risks to develop innovative ideas.</li><li>
Solve moderately complex problems within your expertise and assist with issues outside the department.</li><li>
Oversee operational activities to support the department's short-term goals and manage multiple projects involving cross-functional representatives.</li><li>
Recognize development needs in others, collaborate to create development plans, and manage the performance of direct reports through goal setting, coaching, and ongoing assessment.</li><li>
Solicit input, explain complex concepts, and persuade others to adopt a point of view while effectively sharing your own perspective and rationale.</li><li>
Provide technical engineering oversight for project execution plans and engineering studies for equipment component installation.</li><li>
Support programs and systems with procedures and training, ensuring compliance with regulatory and company requirements, including SOPs, cGMP, safety, quality, OSHA, and other standards.</li><li>
Develop strategies and methods to improve preventive maintenance processes and procedures, enhancing equipment performance and conducting equipment evaluations for new or replacement needs.</li><li>
Facilitate equipment-based Root Cause Failure Analysis (RCFA) investigations, govern maintenance planning and scheduling, foster teamwork, encourage colleague development, and provide salary planning and change management recommendations.</li><li>
Support Manager Engineering in day to day functioning of the Engineering department.</li><li>
To design and implement preventive, predictive , breakdown and shutdown maintenance schedules and execution thereof.</li><li>
To Support Manager Engineering in Annual Engineering budget and keeping track of expenses, monitoring.</li><li>
Liaison with all applicable Government Offices such as Electricity Board, Public Works Department, Factory Inspectorate &amp; Boilers, Industrial Development Corporation office, Meterology etc.</li><li>
Ensure statutory compliances required under the different enactments administered by the above offices.</li><li>
To identify, study, propose and implement energy saving cost reduction, automation productivity improvement measures in the department.</li><li>
Project Mangement - To execute projects for expansion/modification as and when necessary.</li><li>
To oversee installation of new Machineries and decommissioning of machineries /equipments to be replaced.</li><li>
To guide, plan and mange Plant wide maintenance activities, including devising and reviewing solutions to problems in order to support continuity of operations and compliance with CGMP and SOPs</li><li>
To carry out validations, IQ, OQ, DQ, in respect of engineering dept machineries and equipment's.</li><li>
To guide Engineers in maintenance activities to optimize resources and minimum/Budgeted production downtime.</li><li>
To evaluate vendors/suppliers /service providers for various Engineering services and recommend for services / contracts / AMCs.</li><li>
To supervise and verify the bills/work of the vendors/contractors/service providers</li><li>
To provide engineering support to EHS dept in carrying out Plant safety audits/inspections and to take appropriate corrective actionsin case of any unsafe conditions.</li><li>
To carry out departmental orientation and induction of personnel.</li><li>
To inculcate good engineering Practices amongst the dept personnel.</li><li>
Improve safe work conditions and safe working practices to have zero accidents and environment friendly operations.</li><li>
Adherence to local legal requirements, EHS policy and EHS standards/ programs/ SOPs to ensure compliance and improve the safety culture.</li><li>
Participation in safety meetings, EHS programs and EHS events and proactively report and address EHS issues and Near Misses.</li><li>
To ensure adherence and compliance to ISO 9001/14001, OHSAS 18001 and ICH requirements.</li></ul><div></div><div>
Here Is What You Need (Minimum Requirements)</div><ul><li>
Qualification: BE Mechanical</li><li>
10 to 15 years' experience in maintenance of a pharmaceutical unit. Solid dosage unit experience will be preferred.</li><li>
Strong understanding of Process Safety Management elements.</li><li>
Proficiency in Enterprise Asset Management Solutions or other CMMS applications.</li><li>
Thorough knowledge of cGMP (current Good Manufacturing Practices), FDA regulations, and current pharmaceutical industry standards.</li><li>
Strong people management experience.</li><li>
Excellent communication and leadership skills.</li></ul><div></div><div>
Bonus Points If You Have (Preferred Requirements):</div><ul><li>
Master's degree with relevant pharmaceutical experience.</li><li>
Industry experience with preventive and predictive maintenance programs.</li><li>
Experience in equipment-based Root Cause Failure Analysis (RCFA) investigations.</li><li>
Ability to develop and establish strategies and methods that improve preventive maintenance processes and procedures.</li><li>
Experience in providing technical engineering oversight to develop project execution plans and associated engineering studies for equipment component installation.</li></ul>
<br>
Work Location Assignment: On Premise<div></div><div><br>
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.</div><div></div>
Engineering</div><div></div>

Manager - Maintenance

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