Urwah Admin

Sandoz

<div>
 
 Job Description
 
 
 
 
 Major accountabilities:
 
 
 
 <ul>
 <li>
 Oversight of all production and testing activities, ensures compliance with cGxP, incl. data integrity and eCompliance
 </li>
 <li>
 Support exception investigations
 </li>
 <li>
 Review and approval of production, QC, and AS and T records
 </li>
 <li>
 MBR review
 </li>
 <li>
 Support OpEx improvement projects Qualified Person
 </li>
 <li>
 Executes batch release in compliance with registration
 </li>
 <li>
 Reporting of technical complaints / adverse events / special case scenarios related to Sandoz products within 24 hours of receipt
 </li>
 <li>
 Distribution of marketing samples (where applicable)
 
 
 </li>
 </ul>
 
 Key Performance Indicators
 
 
 
 <ul>
 <li>
 On-time and GMP-compliant release of dosage forms
 </li>
 <li>
 No Complaints about inspections by authorities in your own area of responsibility without these being noticed and communicated beforehand.
 </li>
 <li>
 Successfully Support continuous improvement Projects
 </li>
 <li>
 Executes batch release in compliance with registration
 
 
 </li>
 </ul>
 
 Minimum Requirements
 
 
 
 Work Experience:
 
 
 <ul>
 <li>
 Critical Negotiations.
 </li>
 <li>
 Functional Breadth.
 </li>
 <li>
 Project Management.
 </li>
 <li>
 People Leadership.
 </li>
 <li>
 Collaborating across boundaries.
 </li>
 <li>
 Operations Management and Execution.
 
 
 </li>
 </ul>
 
 Skills
 
 
 
 <ul>
 <li>
 Continuous Learning.
 </li>
 <li>
 Dealing With Ambiguity.
 </li>
 <li>
 Employee Performance Evaluations.
 </li>
 <li>
 Gmp Procedures.
 </li>
 <li>
 People Management.
 </li>
 <li>
 QA (Quality Assurance).
 </li>
 <li>
 Quality Control (QC) Testing.
 </li>
 <li>
 Quality Standards.
 </li>
 <li>
 Self-Awareness.
 </li>
 <li>
 Technological Expertise.
 </li>
 <li>
 Technological Intelligence.
 
 
 </li>
 </ul>
 
 Languages
 
 
 
 <ul>
 <li>
 English.
 </li>
 </ul>
</div>

Sr. Quality Operations Coordinator

<div>Major accountabilities:
<ul><li>Define current and future portfolio for Gulf &amp; Levant and Saudi markets in cooperation with internal interfaces
</li><li>Provide input into 5-year Strategic Plan for Gulf &amp; Levant and Saudi countries
</li><li>Ensure timely preparation of submission plans and their implementations
</li><li>Co-ordinate between countries&rsquo; portfolio lead, marketing, supply chain and DRA to prepare business cases for portfolio projects, portfolio review meetings and for senior management approval
</li><li>Drive launch excellence / pre-launch evaluation and apply best practices to ensure new launches are successful on country level with high regional scale.
</li><li>Be the primary contact with regional portfolio team to evaluate local launched in G&amp;L and Saudi and adapt regional portfolio strategies to local market needs
</li><li>Design strategic business development priorities at each year, to drive the profitable growth of Sandoz in GL &amp; SA, and contribute the other Sandoz strategic priorities
</li><li>Lead business case development, using financial modelling and valuation analyses incorporating probability, cost, budget impacts, and returns to allow for optimal strategic and investment decision making
 </li></ul>Minimum Requirements:
<ul><li>Graduate degree in pharmaceuticals, Medicine, business or finance desirable
</li></ul><ul><li>Min. 7 years+ total experience including 5 years as Product / Portfolio Manager
</li></ul><ul><li>Fluent in English and Country language
 </li></ul>Skills:
<ul><li>Strong analytical marketing management experience (senior brand manager level or above
&bull; Cross-functional working
&bull; Project Management
&bull; Complex stakeholder management
&bull; Senior Management operating level
&bull; Key Account Management
&bull; Pharma Industry and Generics Retail or Wholesale knowledge
&bull; Marketing Insights / Analytics skills
&bull; Objective Evaluation and Decision Making
&bull; Communication Skills
</li></ul>Why Sandoz?
Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, provided more than 900 million patient treatments across 100+ countries in 2024 and while we are proud of this achievement, we have an ambition to do more!
With investments in new development capabilities, production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.
Our momentum is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills, experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is supported!
 Languages :
<ul><li>English.</li></ul></div>

Portfolio & Launch Manager, GLS

<div>Your Key Responsibilities:
Your responsibilities include but not are limited to:
<ul><li>Develop and deliver forecasting solutions for internal stakeholders, combining qualitative insights and quantitative analytics to support data-driven decision-making.
</li></ul><ul><li>Build bottom-up and top-down forecasts using internal data, IQVIA, and local databases for Region Europe, while tracking forecast accuracy through defined KPIs.
</li></ul><ul><li>Collaborate cross-functionally to gather, validate, and integrate data inputs, ensuring consistency and reliability across forecasts and portfolio analyses.
</li></ul><ul><li>Support multiple geographies (Region, Clusters, Countries) in forecast creation, portfolio database maintenance, and strategic portfolio reviews.
</li></ul><ul><li>Enhance forecasting processes and deliverables by driving automation, improving quality and productivity, and translating business needs into scalable solutions.
</li></ul><ul><li>Mentor junior team members , contribute to proposal development, and lead knowledge-sharing initiatives, while ensuring compliance with internal SOPs and Sandoz values.
</li></ul><ul><li>Adhere to Sandoz values and behaviors : Team up to break barriers, Be ambitious as our purpose, Lead by example and Be open-minded.
</li></ul>What you'll bring to the role:
Minimum Requirements:
<ul><li>5&ndash;7 years of relevant experience in applying diverse forecasting techniques for inline, pipeline, and BD&amp;L products/brands, including trend-based forecasting. Strong understanding of disease areas and therapy domains, and their application in forecast development.
</li></ul><ul><li>Proficient in Advanced Excel for model building, with expertise in automation to improve usability and in using data visualization to communicate forecast insights effectively.
</li></ul><ul><li>Skilled in data management and trend analysis , applying quantitative analytics to generate insights and continuously refine forecast catalogues.
</li></ul><ul><li>Well-versed in Market Access, Healthcare, and Pricing &amp; Reimbursement policies , with the ability to integrate these into forecasting models. Strong background in secondary research to support and validate forecasting assumptions.
</li></ul><ul><li>Hands-on experience with key industry datasets such as IQVIA, Evaluate, IPD, and DRG, enabling robust and data-driven forecasting.
</li></ul><ul><li>Expertise in forecast storyboarding , synthesizing key insights supported by data. Proficient in business analysis, analog analysis, and quantitative techniques to enhance forecast accuracy.
</li></ul><ul><li>Experience in the generics and biosimilars industry is an added advantage.
</li></ul>Desirable Requirements:
<ul><li>Strong learning agility, Problem solving and solution-based mindset. Strong verbal and written communication, presentations skills, storyboarding. Ability to grasp functional processes and tailor solutions accordingly
</li></ul><ul><li>Effective in project management and stakeholder management. Successful in leading small engagements. Experience of working in matrix environment and multicultural teams
</li></ul>You'll receive:
Breakdown of benefits received in this role. Include flexible working, learning and development opportunities as well.
Why Sandoz?
Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, touched the lives of almost 500 million patients last year and while we are proud of this achievement, we have an ambition to do more!
With investments in new development capabilities, state-of-the-art production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.
Our momentum and entrepreneurial spirit is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is encouraged!
The future is ours to shape!
#Sandoz</div>

Manager - Forecasting

<div>Your Key Responsibilities
Your responsibilities include, but are not limited to:
<ul><li>Develop engaging content for internal channels such as emails, newsletters, intranet, and Viva Engage.
</li><li>Translate complex technology and leadership topics into simple, employee-friendly messaging.
</li><li>Create visual assets including infographics, banners, and videos aligned with brand guidelines.
</li><li>Support stakeholder engagement to gather stories, updates, and success narratives.
</li><li>Manage and optimize internal communication platforms like Teams, SharePoint, and Viva Engage.
</li><li>Plan and publish content consistently, ensuring quality and relevance.
</li><li>Coordinate communications for tech events, townhalls, and webinars including pre-event, live, and post-event messaging.
</li><li>Track engagement metrics, create dashboards, and use insights to improve communication impact.
</li></ul>KPI:
 
Dashboard adoption and engagement rates across internal platforms.
What You&rsquo;ll Bring to the Role
Essential Requirements
<ul><li>Bachelor&rsquo;s degree in communications, Public Relations, Marketing, or a related field.
</li><li>4&ndash;6 years of experience in internal communications, employee engagement, or community management.
</li><li>Experience working in global or matrixed organizations.
</li><li>Strong writing and editing skills tailored to diverse audiences.
</li><li>Proficiency with Microsoft 365 tools (Teams, SharePoint, Viva Engage).
</li><li>Basic design skills (Canva, PowerPoint, Adobe tools).
</li><li>Strategic thinker with a proactive approach to communications.
</li><li>Strong stakeholder management and analytical skills.
</li><li>High cultural sensitivity and ability to collaborate across geographies.
</li><li>Fluent in English (verbal and written).
</li></ul>Desirable Requirements
<ul><li>Proficiency in an additional language.
</li><li>Experience in tech communications or digital transformation environments.
</li></ul>You&rsquo;ll Receive
<ul><li>Flexible working arrangements.
</li><li>Access to global learning and development programs.
</li><li>Opportunities to work in a collaborative, diverse, and inclusive environment.
</li><li>Career growth in a transformation-driven global organization.
</li></ul>Why Sandoz?
Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, provided more than 900 million patient treatments across 100+ countries in 2024. While we are proud of this achievement, we have an ambition to do more!
With investments in new development capabilities, production sites, acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines&mdash;sustainably.
Our momentum is powered by an open, collaborative culture driven by our talented and ambitious colleagues. In return for applying their skills, they experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and personal growth is supported.
Join us!</div>

Global IT User Engagement Specialist, Technology Management Office (TMO), Technology

<div>Global Head of Clinical Development &amp; Patient Safety Solutions
Sandoz continues to go through an exciting and transformative period as a global leader and pioneering provider of sustainable Biosimilar and Generic medicines. As we continue down this new and ambitious path, unique opportunities will present themselves, both professionally and personally. Join us, the future is ours to shape!
Job Summary
The Global Head of Clinical Development &amp; Patient Safety Solutions is focused on ensuring that Clinical Development &amp; Patient Safety stakeholders successfully achieve their goals using the technology systems provided. This role involves closely working with Clinical Development &amp; Patient Safety stakeholders to understand their evolving needs, challenges, opportunities, and priorities, and ensuring that their automation and information needs are met by collaborating with other members of their functional unit and/or other functional units. Stakeholder Success Leads play a crucial role in representing the face of Technology to the stakeholder community they serve.
Your Key Responsibilities
Your responsibilities include, but are not limited to:
<ul><li>Stakeholder Engagement
<ul><li>Facilitate effective dialogues to identify business issues, challenges, and opportunities that can be addressed through technology.
</li><li>Align Clinical Development &amp; Patient Safety technology strategy with business directives and needs.
</li><li>Manage Technology priorities for the Clinical Development &amp; Patient Safety business area.
</li><li>Develop and maintain relationships with key Clinical Development &amp; Patient Safety leaders to ensure alignment of Technology services with Clinical Development &amp; Patient Safety objectives.
</li><li>Conduct regular meetings with Clinical Development &amp; Patient Safety stakeholders to gather requirements and feedback.
</li></ul></li></ul><ul><li>Project Management
<ul><li>Ensure the capture of functional requirements and design specifications for Clinical Development &amp; Patient Safety technology solutions.
</li><li>Coordinate technology delivery of the Clinical Development &amp; Patient Safety&rsquo;s IT portfolio and priorities, ensuring projects are on schedule and outcomes are of high quality.
</li><li>Collaborate with Technology teams to develop and implement solutions that address Clinical Development &amp; Patient Safety stakeholder needs.
</li><li>Monitor and report on the progress of Clinical Development &amp; Patient Safety Technology projects and initiatives.
</li><li>Implement risk management strategies to ensure project success.
</li></ul></li></ul><ul><li>Budget and Resource Optimization
<ul><li>Meet operational and project budgets.
</li><li>Effectively lead and manage the Clinical Development &amp; Patient Safety Stakeholder Success team.
</li><li>Identify, manage, and improve vendor relationships.
</li><li>Optimize resource allocation to ensure maximum efficiency and cost-effectiveness.
</li><li>Develop and manage financial forecasts and budgets for technology projects.
</li></ul></li></ul><ul><li>Innovation and Improvement
<ul><li>Identify opportunities for technological innovation within Clinical Development &amp; Patient Safety.
</li><li>Continually update personal knowledge of industry trends and developments to enhance solutions provided to Clinical Development &amp; Patient Safety.
</li><li>Maintain a detailed understanding of how Clinical Development &amp; Patient Safety processes are operationalized within technology tools.
</li><li>Encourage and support the adoption of new technologies and processes.
</li><li>Lead pilot programs for new technology solutions and assess their effectiveness.
</li></ul></li></ul><ul><li>Communication and Coordination
<ul><li>Drive the adoption of the Technology Organization&rsquo;s standards and solutions.
</li><li>Ensure smooth execution and maintain clear lines of communication between cross-functional Technology teams and Clinical Development &amp; Patient Safety.
</li><li>Coordinate with other functional units to ensure alignment and integration of technology solutions.
</li><li>Develop and maintain communication channels to provide regular updates and feedback to stakeholders. 
</li></ul></li></ul>Minimum Requirements
What you&rsquo;ll bring to the role:
Experience:
<ul><li>10-15 years&rsquo; experience in a Clinical Development &amp; Patient Safety stakeholder engagement or business analyst role.
</li><li>Proven track record in project management and stakeholder satisfaction related to Clinical Development &amp; Patient Safety.
</li><li>Tenure in a management role overseeing complex projects.
</li><li>Proven track record of developing and implementing Clinical Development &amp; Patient Safety technology strategies.
</li><li>Demonstrated ability to lead and mentor a dispersed technology team.
</li><li>Experience in regulatory and compliance environments, understanding the implications for technology solutions and data management in global markets.
</li><li>History of successful stakeholder engagement and relationship management.
</li></ul>Skills:
<ul><li>Expert knowledge of Clinical Development &amp; Patient Safety business processes and complexities
</li><li>Strong experience implementing and managing IT technologies supporting key business capabilities, incl. Clinical Trial Management Systems (CTMS), Electronic Data Capture (EDC), Safety Databases (e.g., Argus, ArisGlobal), and Signal Detection, etc.
</li><li>Deep understanding of clinical trial processes, regulatory requirements (e.g., GxP, ICH guidelines), and safety data management.
</li><li>A proven track record of implementing digital solutions to enhance business processes and experience in leading innovative projects that leverage AI, machine learning, and / or other advanced technologies to improve operational efficiency
</li><li>Excellent communication &amp; presentation skills
</li><li>Networking with key business and IT stakeholders and ability to present to senior stakeholder groups.
</li><li>Strong teamwork and interpersonal skills at team and management levels, with the ability to establish and maintain a high level of trust and confidence.
</li><li>Excellent negotiation skills including vendor management experience.
</li><li>Analytical, process-oriented with a keen interest to drive continuous improvements.
</li><li>Acting as a role model for all people within the organization.
</li><li>Strong can-do attitude and results-focused, with capability to think strategically.
</li></ul>Why Sandoz?
Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, provided more than 900 million patient treatments across 100+ countries in 2024 and while we are proud of this achievement, we have an ambition to do more!
With investments in new development capabilities, production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.
Our momentum is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is supported!
Join us!
#Sandoz</div>

Global Head of Clinical Development & Patient Safety Solutions

<div>Major accountabilities:
<ul><li>Ensure the operational conversion of the BPA strategic goals within a dedicated area of the business -Provide management with accurate, relevant business analysis to support monthly operational reviews and ad-hoc requests, and ensure timely and accurate information gathering.
</li><li>Perform analysis to evaluate risks or opportunities; make recommendations to mitigate these risks. Manage and provide financial analysis and decision making support for a investment/project in a domain -Ensure ongoing business performance is appropriately monitored and measured, and drive early warning for re-direction of resources with Business Partners.
</li><li>Provide accurate operational information and advice to support the annual budgeting, rolling forecast and Strategic Planning processes.
</li><li>Ensure integrity of data provided by commercial teams, and provides value added; provides recommendations on forecast accuracy improvement.
</li><li>Provide well managed and quality financial analysis in order to improve business case proposals and profitability tracking.
</li><li>Continually improve and streamline existing management reporting processes and support the definition and implementation of lean processes to meet the changing demands of the business.
</li><li>May supervise the performance and development of a small team of BPA specialists.
</li><li>Reporting of technical complaints / adverse events / special case scenarios related to Sandoz products within 24 hours of receipt -Distribution of marketing samples (where applicable) 
 </li></ul>Minimum Requirements:
 
Work Experience:
<ul><li>Minimum 4 years of experience and Plant Finance and SAP. 
</li></ul>Why Sandoz?
Generic and Biosimilar medicines are the backbone of the global medicines industry. Sandoz, a leader in this sector, touched the lives of almost 500 million patients last year and while we are proud of this achievement, we have an ambition to do more!
With investments in new development capabilities, state-of-the-art production sites, new acquisitions, and partnerships, we have the opportunity to shape the future of Sandoz and help more patients gain access to low-cost, high-quality medicines, sustainably.
Our momentum and entrepreneurial spirit is powered by an open, collaborative culture driven by our talented and ambitious colleagues, who, in return for applying their skills experience an agile and collegiate environment with impactful, flexible-hybrid careers, where diversity is welcomed and where personal growth is encouraged!
The future is ours to shape!</div>

Assistant Manager - BPA

<div>Major accountabilities:
<ul><li>Validation Expert -Support Product Steward in maintaining the process control strategy.
 </li><li>Translate applicable process parameters and the process control strategy into a focused validation plan for process validation.
</li><li>Provide technical expertise and facilitate establishment of Quality Risk Assessment (as needed).
</li><li>Support site validation planning by writing and maintaining master plans for processes, cleaning, packaging processes and ongoing verification for processes and cleaning (as applicable).
</li><li>Support process validation lifecycle activities by ensuring a state of control is maintained through ongoing process verification (OPV).
 </li><li>Ensure that appropriate variables are identified for on-going monitoring as a contributor to quality risk management activities.
</li><li>Work in close collaboration with development organization (or sending site) for technical transfers and new product launches to ensure that knowledge is transferred, control strategies are appropriate, risks are analyzed and controlled and to ensure that commercial processes are validation readyScientist MSAndT -Comply with applicable GxP regulations, SOPs, HSE, ISEC And other Sandoz Guidelines in the laboratory and, -Maintain up-to-date documentation of laboratory work carried out including documentation storage and archiving.
</li><li>Contribute to and maintain lab instructions, SOPs, templates.
</li><li>Support, qualification and calibration of lab / pilot equipment with accompanying documentation, schedule and perform routine maintenance.
</li><li>Contribute to the evaluation of new equipment.
</li><li>Design, execute and document experiments (formulation / analytical tests etc.) for products assigned in the context of process transfer, process improvement and process validation.
</li><li>Prepare and review appropriate GxP documentation including change requests.
</li><li>Participate in Tech Transfer activities from laboratory to industrial scale, support validation activities.
</li><li>Identify improvement options of current processes, propose business cases.
</li><li>Reporting of technical complaints / adverse events / special case scenarios related to Sandoz products within 24 hours of receipt -Distribution of marketing samples (where applicable)
 </li></ul>Key performance indicators:
<ul><li>Meet established validation milestones according to approved validation plans.
</li><li>Audit and inspection outcomes as a measure of validation compliance with global regulatory expectations.
</li><li>Timing and quality of technical reports.
</li>Timely and successful implementation of transfer activities (e.g. lab-to-lab transfer in launches). 
<li>
 </li></ul>Minimum Requirements: 
 
Work Experience:
<ul><li>Fix-its/Turnarounds.
</li><li>Project Management.
</li><li>Collaborating across boundaries.
</li><li>Operations Management and Execution.
 </li></ul>Skills:
<ul><li>Assembly Language.
</li><li>Change Control.
</li><li>Chemical Engineering.
</li><li>Chemistry.
</li><li>Continual Improvement Process.
</li><li>Cost Reduction.
</li><li>Data Analytics.
</li><li>Electronic Components.
</li><li>General Hse Knowledge .
</li><li>Including Gdp.
</li><li>Knowledge Of Capa.
</li><li>Knowledge Of Gmp.
</li><li>Lean Manufacturing.
</li><li>Manufacturing (Production).
</li><li>Manufacturing Process.
</li><li>Pharmaceutics.
</li><li>Process and Cleaning Validation.
</li><li>Process Control.
</li><li>Process Engineering.
</li><li>Risk Management.
</li><li>Root Cause Analysis (Rca).
</li><li>Scheduler.
</li><li>Six Sigma.
</li><li>Sop (Standard Operating Procedure).
 </li></ul>Languages :
<ul><li>English.</li></ul></div>

Validation Expert

Join Sandoz and explore 11   exciting career opportunities. They're hiring for various roles with options for remote or on-site work. Apply today and become part of their innovative team.