Urwah Admin

Sandoz

<div>Your Key Responsibilities:
Your responsibilities include, but not limited to:
Key Responsibilities:
<ul><li>Technical Support to Internal Sites and CMOs Act as Technical Expert for assigned internal manufacturing sites or CMOs, ensuring process capability and maintaining products in a validated state.
</li><li>Apply science- and risk-based approaches to ensure sustainable product quality.
</li><li>Ensure availability of all relevant technical documentation (protocols, reports, risk assessments, concept papers, scientific justifications) ahead of planned site activities.
</li></ul>Product &amp; Technical Stewardship
<ul><li>Maintain oversight and deep understanding of the entire manufacturing process across the product lifecycle.
</li><li>Identify and monitor CQAs, CMAs, and CPPs to ensure process robustness and product quality.
</li><li>Analyze manufacturing data (OPV, CPV, APQR) to assess state of control and recommend improvements.
</li><li>Evaluate technical changes, assess feasibility, and define scope/design of technical batches.
</li><li>Contribute to registration strategy and align regulatory timelines for changes, transfers, launches, and deviations.
</li><li>Lead/support root cause investigations for product/process failures and drive remediation/improvement initiatives.
</li><li>Collaborate cross-functionally with Quality, Operations, Engineering, and Development teams.
</li><li>Share best practices and lessons learned across divisions and sites.
</li></ul>Validation Support
<ul><li>Define and implement validation strategies and supporting documentation.
</li><li>Maintain validation oversight and ensure products remain in a validated state.
</li><li>Review QRAs and challenge control strategies based on CQAs, CPPs, and CMAs.
</li><li>Ensure technical batches generate sufficient process knowledge.
</li><li>Support creation and review of validation protocols and reports.
</li><li>Contribute to revalidation planning and documentation.
</li></ul>Launch &amp; Transfer Support
<ul><li>Participate in supplier/product evaluation and selection processes.
</li><li>Gather and document technical information on manufacturing capabilities of sites/CMOs.
</li><li>Provide data and documentation for tech transfer activities, leveraging existing process knowledge.
</li><li>Define product acceptance criteria and monitor performance post-transfer.
</li><li>Ensure successful, well-documented product transfers and launches.
</li><li>Actively support governance processes for product launch and transfer.
</li></ul>Interface with Development
<ul><li>Ensure new products and processes are designed for commercial scalability and lifecycle sustainability.
</li><li>Provide input at formal stage gates during development and up to first OPV/APQR.
</li><li>Support development of control strategies that meet regulatory and operational requirements.
</li></ul>Manufacturing &amp; Operational Excellence
<ul><li>Lead design and control optimization projects to improve process robustness and sustainability.
</li><li>Provide SME-level expertise for process characterization of biologics manufacturing.
</li><li>Prepare high-quality design and operational documents.
</li><li>Proactively take on challenging projects driven by evolving regulatory requirements, audits, and compliance needs.
</li></ul>Training
<ul><li>Own and maintain the training curriculum relevant to the job description and responsibilities.
</li></ul>What you'll bring to the role:
Minimum Requirements:
Ideal Background
Education (minimum/desirable):
<ul><li>Experience in biologics manufacturing including cell culture, fermentation, purification, and formulation processes
</li><li>Post Graduate in Pharmacy/Biology/Bio tech/Relevant Life Sciences/ Ph.D. in Pharmaceutical Technology (preferred)
</li></ul>Languages
<ul><li>Fluent in English &amp; Languages in the Region
</li></ul>Relevant Experiences
<ul><li>8-12 years of relevant experience in manufacturing. Additional specialist experience is preferred
</li><li>Strong knowledge of regulatory guidelines: USFDA, EMA, ICH, ASTM, SUPAC.
</li><li>Expertise in QbD, DoE, Minitab, and statistical analysis.
</li><li>Ability to prepare high-quality design and operational documents for equipment qualification, verification, and continuous process validation.
</li><li>Excellent communication and cross-functional collaboration skills.
</li><li>Ability to manage multiple complex projects in a global matrix environment.
</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>

Technical Expert MS&T Bio Similar/ Large Molecules DS/DP

<div>Major accountabilities:
<ul><li>Planning and supporting PQR/APQR activities -Support site qualification and validation activities (planning, advising, review) -Implementation of Quality Systems (incl. documentation management) -Supplier management activities (agreements, oversight, audit) -Preparation/support and coordination of CAPA/follow-up -Audit and inspection preparation and support -Change control review/approval -Ensure local DI and eCompliance oversight (training, inspections, plan, risk ID etc.) -Ensure process quality assurance acc.
</li><li>to regulations -QP declaration review and approval -KPI trending -Ensure applications, certificate maintenance etc. to local HA -SPOC for communication with HA, GCA / One voice / consolidated approach / synergies for all sites within same HA jurisdiction / country -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>Ensures planning and successfully supports PQR/APQR activities -Successfully carries out site qualification and validation activities (planning, advising, review) -Supports the implementation of Quality Systems (incl. documentation management); Ensure local DI and eCompliance oversight (training, inspections, plan, risk ID etc.) -Ensure process quality assurance according to regulations
</li></ul>Minimum Requirements:
Work Experience:
<ul><li>QC/ QA in pharmaceutical ind./ biotech with environmental monitoring &amp;.
</li><li>cleanliness zones.
</li><li>Functional Breadth
</li></ul>Skills:
<ul><li>Action Oriented.
</li><li>Continuous Learning.
</li><li>Dealing With Ambiguity.
</li><li>Functional Skills.
</li><li>Gmp Procedures.
</li><li>Process Optimization.
</li><li>QA (Quality Assurance).
</li><li>Quality Standards.
</li><li>Self-Awareness.
</li><li>Technological Expertise.
</li><li>Technological Intelligence.
</li><li>GxP.
</li><li>Industry standards.
</li><li>Compliance requirements.
</li></ul>Languages:
<ul><li>English.</li></ul></div>

Quality Compliance Coordinator (Temp.)

<div>Major accountabilities:
<ul><li><h3 class="jobSectionHeader">Major accountabilities:
</h3></li><li>Drive Competitive Sales Growth
</li><li>Identify and prioritize high-potential customers through data analysis (HCPs and stakeholders) who influence prescription decisions
</li><li>Drive sales performance through the skillful orchestration of positive customer experiences
</li><li>Engage and Build Relationships
</li><li>Engage in value-based conversations (in-person and virtually) to understand critical customer challenges, decision-drivers, pain points and opportunities
</li><li>Personalize and orchestrate customer engagement journeys for target HCPs by reflecting customer preferences, leveraging available content and multiple engagement channels
</li><li>Build engagement by working in partnership with HCPs to develop a sustained collaboration over time for Sandoz
</li><li>Deliver memorable, customer-centric experiences beyond clinical differentiation by listening to their needs and understanding their healthcare environment
</li><li>Establish effective working relationships with opinion leaders and top medical influencers (at territory level) and challenge current behaviors in order to improve the patient journey (right patient, right time)
</li><li>Develop Deep Customer Insights and Understanding
</li><li>Gather insights on the customer&rsquo;s business to uncover what is important to them
</li><li>Follow up on customer feedback and translate responses into actions that create additional value and exceed expectations
</li><li>Leverage available data sources to create, dynamically prioritize and adjust relevant territory, account and customer interaction plans
</li><li>Share customer insights with relevant internal stakeholders on an ongoing basis to support the development of product-and indication-related content, campaigns and interaction plans
</li><li>Deliver Value to Customers and Patients
</li><li>Collaborate compliantly with cross-functional teams to design and implement solutions that address unmet customer and patient needs
</li><li>Act as a trusted partner to the customer for the purpose of helping them run their business; listen to learn; strive to deepen the relationship in a compliant and ethical manner; position themselves to create value-add solutions .
</li><li>Act with integrity and honesty by treating customers and colleagues in a transparent and respectful manner with clear intent.
</li><li>When facing ethical dilemmas, do the right thing and speak up when things don't seem right.
</li><li>Live by Sandoz Code of Ethics and Values and Behaviors.
</li></ul><h2 class="jobSectionHeader">What you&rsquo;ll bring to the role:
</h2><ul><li>Location needed: Cairo
</li><li>Bachelor's degree in Pharmacy or any related field.
</li><li>Fresh to + 2 years of experience in pharmaceutical sales field in Retail/OTC.
</li><li>Demonstrate strong selling competencies and proven sales performance track record.
</li><li>Strong Sales and negotiation skills.
</li><li>Strong communication and interpersonal skills.
</li><li>Very good command of English Language.
 </li></ul>Skills:
<ul><li>Account Management.
</li><li>Commercial Excellence.
</li><li>Communication Skills.
</li><li>Compliance.
</li><li>Conflict Management.
</li><li>Cross-Functional Coordination.
</li><li>Customer Insights.
</li><li>Ethics.
</li><li>Healthcare Sector.
</li><li>Influencing Skills.
</li><li>Negotiation Skills.
</li><li>Selling Skills.
</li><li>Technical Skills.
</li></ul><h3 class="jobSectionHeader">Why Sandoz?
</h3>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!
Commitment to Diversity &amp; Inclusion:
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
#Sandoz</div>

Medical Representative

<div>Your Key Responsibilities:
Your responsibilities include, but not limited to:
<ul><li>Data Quality &amp; Governance
</li></ul>Ensure completeness, accuracy, and consistency of data in SANITY across key business objects (e.g., Product Targets, BD Deals, Portfolio Projects). Proactively identify and resolve data issues using dashboards and reports.
<ul><li>Operational Process Support
</li></ul>Support the execution of business processes such as GPC preparation, BD&amp;L governance steps, and forecasting cycles by maintaining high-quality data inputs and outputs.
<ul><li>Business Collaboration
</li></ul>Work closely with stakeholders across Platforms, BD&amp;L, Launch Excellence, Countries and Regions to understand data needs, provide guidance, and ensure alignment with evolving processes.
<ul><li>Reporting &amp; Insights
</li></ul>Maintain and enhance dashboards and reports that support transparency and decision-making. Provide insights to business teams based on data trends and quality indicators.
<ul><li>System Coordination
</li></ul>Monitor data flows between SANITY and other systems (e.g., SAP, GloRiA), ensuring correct transfer of data. Flag and follow up on interface issues in collaboration with relevant teams.
<ul><li>Documentation &amp; Best Practices
</li></ul>Maintain clear documentation of data processes and standards. Promote adherence to governance guidelines and support onboarding of new users.
What you'll bring to the role:
Minimum Requirements:
Education, Qualifications and Experience
<ul><li>Bachelor&rsquo;s degree in Business Administration, Operations Management, Data Management, or a related field.
</li><li>3&ndash;5 years of experience in business operations, data quality, or portfolio support roles, ideally within the pharmaceutical or life sciences industry.
</li><li>Familiarity with enterprise systems such as SANITY and SAP and understanding data governance in a business context.
</li><li>Strong analytical skills and attention to detail, with a focus on operational execution.
</li><li>Experience working in cross-functional and global teams.
</li></ul>Skills and Expertise
<ul><li>Solid understanding of commercial and portfolio processes in pharma or similar industries.
</li><li>Strong coordination and project support skills, with the ability to work across development, commercial, and operations teams.
</li><li>Experience supporting data-driven business processes such as forecasting, governance, and launch planning.
</li><li>Excellent communication and stakeholder engagement skills.
</li><li>Ability to manage multiple priorities independently and deliver high-quality outcomes.
</li></ul>Personal Attributes
<ul><li>Strong interpersonal, presentation, and influencing skills.
</li><li>Proven ability to work effectively in complex matrix organizations and manage diverse stakeholders.
</li><li>Proactive, solution-oriented, and able to take initiative in driving operational improvements.
</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>

Data Steward - SANITY Business Operations

<div>Major accountabilities:
<ul><li>Technical Transfer Lead -Review and update Quality Risk Assessment (QRA) prior to transfer and prior to validation, adapt control strategy if needed.
</li><li>Review first APQR after transfer to ensure adequate product performance -Ensure that all relevant technical information and documentation for validation is available.
</li><li>Define pre-validation / validation strategy incl. process, cleaning, packaging and supportive studies (e.g., hold times).
 </li><li>Coordinate technical, regulatory and validation batches at site.
</li><li>Support Validation Lead / Validation Expert in creation of validation protocol and report.
</li><li>Product Steward And -Maintain the oversight and knowledge for entire manufacturing process performed on site and throughout the entire commercial lifecycle, since transfer from development to date, act as SPOC.
</li><li>Create and maintain a product specific Quality Risk Analysis (QRAs).
</li><li>Monitor all critical variables and key variables as appropriate using statistical analysis and conducting regular product specific data trending.
</li><li>Review APQR and decide on state of control.
</li><li>Technical Steward -Act as the SPOC for the interface with global MSAndT network and with technical development organization, for the corresponding global activities, to define and implement new technical standards for existing and new technologies and equipment.
</li><li>Owns the knowledge of specific pharmaceutical manufacturing process technologies, locally, including any pilot scale, scale up or down, and Design of Experiments (DoE).
</li><li>Provide technical expertise for validation activities around technologies within area of responsibility.
</li><li>Harmonize and optimize technical processes across the site.
</li><li>Validation Lead -Support Product Steward in maintaining the process control strategy.
</li><li>Provide technical expertise and facilitate establishment of Quality Risk Assessment (as needed).
</li><li>Define and implement validation strategy (process, cleaning, ongoing verification) and defend to authorities.
</li><li>Overall responsibility for establishment, prioritization, execution and tracking of Validation Master Plan for process, cleaning, packaging validation and ongoing process verification (OPV), ongoing cleaning verification.
</li><li>Senior Scientist MSAndT -Complex projects with deep understanding of development process requirements -Difficult to solve topics (eg.
 </li><li>new by-product investigation, complex deviations) -Cross product alignment in support approach (larger sites) -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:
Cost, C-Sat and productivity targets -Achievement of project plans &amp; milestones -Internal customer satisfaction with quality of services provided -Validation Master Plan (VMP) completed and up to date. 
<ul><li>
 </li></ul> 
Minimum Requirements: 
 
Work Experience:
<ul><li>Fix-its/Turnarounds.
</li><li>Operations Management and Execution.
</li><li>Collaborating across boundaries.
</li><li>Project Management.
 </li></ul>Skills:
<ul><li>Applied Statistics.
</li><li>Assembly Language.
</li><li>Change Control.
</li><li>Chemical Engineering.
</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>Manufacturing Technologies.
</li><li>Process And Cleaning Validation.
</li><li>Process Control.
</li><li>Process Simulation.
</li><li>Risk Management.
</li><li>Root Cause Analysis (Rca).
</li><li>Scientific Method.
</li><li>Six Sigma.
</li><li>Statistical Analysis.
</li><li>Technology Transfer.
 </li></ul>Languages :
<ul><li>English.</li></ul></div>

Technical Expert MS&T OSD

<div>Major accountabilities:
<ul><li>OOx/Deviation handling.
</li><li>CAPA definition -KPI trending -Ensure all activities in compliance with cGxP, incl. data integrity review and approval of analytical data / tests (analytical release) Stability -Stability testing (Projects) &ndash; protocol preparation, evaluation, report preparation.
</li><li>Reporting (Stability plan preparation, trend analysis, evaluation)
</li><li>Performance of Stability studies, protocols and comparative reports for supplier qualification -Review and approval of analytical tests (analytical release)
</li><li>Microbiological QC -Perform Microbiological testing of materials and utilities, environmental and personnel monitoring -Provide expert Support for site qualification and validation activities -Maintain and calibrate equipment incl. plan preparation -Support in supplier qualification -Trending and analysis of KPI/KQI -Support sample planning and sampling execution -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>Job Description:
<ul><li>To prepare, update, and track revisions of laboratory procedures in accordance with current and legal regulatory guidelines.
</li></ul>&middot; To work in compliance with current GMP rules and company procedures.
&middot; To conduct and report necessary activities within the quality management system (OOS/OOT, Deviation Investigation, Change Control, and Corrective and Preventive Actions).
&middot; To perform and report microbiological analyses of raw materials, semi-finished products, finished products, and packaging materials.
&middot; To carry out and report the microbiological method validation and verification studies.
&middot; To implement the environmental monitoring program, evaluate results, and report findings.
&middot; To perform and evaluate the microbiological controls of compressed air systems.
&middot; To perform and evaluate microbiological analyses of the water system.
&middot; To perform microbiological analyses of detergents and disinfectants used.
&middot; To perform, evaluate, and report disinfectant efficacy studies in accordance with pharmacopeia and related standards.
&middot; To prepare all culture media and solutions used in the laboratory according to instructions and to perform growth promotion studies.
&middot; To prepare for and participate in customer and regulatory audits.
&middot; To conduct and report Microbiological Risk Assessments and OPEX studies.
&middot; To perform bulk holding time (BHT) studies, evaluate results, and report findings.
&middot; To ensure the calibration and verification of used equipment are carried out and tracked.
&middot; To support the qualification and calibration processes of laboratory equipment.
&middot; To ensure the regular and effective operation of the microbiology laboratory.
&middot; To ensure the preparation of periodic trend reports and their timely implementation.
&middot; To ensure that laboratory records are accurate and complete.
&middot; To track, prepare, and report reference cultures of microorganisms.
&middot; To perform and report microorganism identifications.
Key performance indicators:
<ul><li>The relevant KPIs that are defined in the Quality Control areas apply: e.g. analytical lead times -Timely and GMP-compliant analysis &amp; documentation of the results.
</li><li>Error rate: Number of OOS (analysis errors) related to the number of analyzes -No complaints about official inspections.
</li><li>Individual performance is assessed using the PMP performance dialog together with the manager
</li></ul>Minimum Requirements:
 
Work Experience:
<ul><li>Functional Breadth.
</li><li>Preferably at least 4 years of experience in a microbiology laboratory, particularly in the pharmaceutical industry (especially in non-sterile manufacturing).
</li><li>Collaborating across boundaries.
</li><li>A GMP environment/equivalent.
</li><li>Bachelor&rsquo;s degree in Microbiology, Biology, Molecular Biology &amp; Genetics, or Bioengineering from the university. 
</li></ul><ul><li>Good command of English (reading, writing, speaking).
</li><li>Knowledge and experience in microbiological analysis techniques (e.g., disinfectant efficacy studies, non-sterile product analysis tests, etc.).
</li><li>Proficiency in MS Office programs.
</li></ul>Skills:
<ul><li>Continuous Learning.
</li><li>Dealing With Ambiguity.
</li><li>Decision Making Skills.
</li><li>Gxp.
</li><li>Industry Standards.
</li><li>Laboratory Equipment.
</li><li>Laboratory Excellence.
</li><li>Quality Control (QC) Testing.
</li><li>Quality Control Sampling.
</li><li>Self-Awareness.
</li><li>Technological Expertise.
</li><li>Total Quality Management.
</li><li>Team-oriented, with strong communication skills, responsible, and detail-oriented.
</li></ul>&middot; Possesses problem-solving and analytical thinking skills.
<ul><li>Able to keep up with the busy work tempo
</li></ul>Languages:
<ul><li>English.</li></ul></div>

QC Microbiology Specialist

Microbiogy Specialist

Join Sandoz and explore 12   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.