Qureos Mentor

Opella

<div><div>Job title: Regulatory Data Model Governance Lead</div><ul><li>
Location: Hyderabad</li></ul><div></div><div>
Opella is the self-care challenger with the purest and third-largest portfolio in the Over-The-Counter (OTC) &amp; Vitamins, Minerals &amp; Supplements (VMS) market globally.</div><div>
Our mission is to bring health in people&rsquo;s hands by making self-care as simple as it should be. For half a billion consumers worldwide &ndash; and counting.</div><div>
At the core of this mission is our 100 loved brands, our 11,000-strong global team, our 13 best-in-class manufacturing sites and 4 specialized science and innovation development centers. Headquartered in France, Opella is the proud maker of many of the world&rsquo;s most loved brands, including Allegra, Buscopan, Doliprane, Dulcolax, Enterogermina, Essentiale and Mucosolvan.</div><div>
As a globally certified B Corp company, we are active players in the journey towards healthier people and planet. Find out more about our mission at <div>www.opella.com</div>.</div><div></div><div><i>
About the job:</i></div><div>
Regulatory Data Model Governance Lead is responsible for establishing and maintaining governance frameworks for regulatory data across the organization. This role ensures data integrity, compliance, and usability in alignment with global regulatory standards (e.g., IDMP, xEVMPD, GxP).</div><div></div><div><i>
Main Responsibilities:</i></div><ul><li><div>
Data Governance Strategy</div></li><li><ul><li><div>
Define and implement regulatory data governance policies and frameworks.</div></li><li><div>
Develop data stewardship models and assign roles (owners, stewards, quality leads).</div></li><li><div>
Align governance with internal standards and external regulatory requirements.</div></li></ul></li><li><div>
Metadata Management</div></li><li><ul><li><div>
Lead metadata capture, lineage tracking, and sensitive data tagging.</div></li><li><div>
Maintain regulatory data catalogs and glossaries.</div></li><li><div>
Ensure discoverability and traceability of metadata across RIM/eDMS systems.</div></li></ul></li><li><div>
Quality and Compliance</div></li><li><ul><li><div>
Define and monitor data quality metrics.</div></li><li><div>
Oversee classification, retention, and access policies for regulatory documents.</div></li><li><div>
Ensure compliance with IDMP, xEVMPD, and other global standards.</div></li></ul></li><li><div>
Change Management</div></li><li><ul><li><div>
Drive adoption of governance practices through training and stakeholder engagement.</div></li><li><div>
Support regulatory intelligence assessments and change impact analysis.</div></li></ul></li><li><div>
Architecture and Integration</div></li><li><ul><li><div>
Contribute to RIM data roadmap, architecture diagrams, and interface specifications.</div></li><li><div>
Collaborate with IT to ensure system interoperability and scalability.</div></li></ul></li></ul><div><i>
About you:</i></div><ul><li><div>
Bachelor&rsquo;s or Master&rsquo;s in IT, Life Sciences, or related field.</div></li><li><div>
5+ years in regulatory data governance or RIM systems.</div></li><li><div>
Deep understanding of pharmaceutical regulatory standards.</div></li><li><div>
Strong leadership, communication, and stakeholder management skills.</div></li></ul><div></div><div><i>
Why us?</i></div><div></div><div>
At Opella, you will enjoy doing challenging, purposeful work, empowered to develop consumer brands with passion and creativity. This is your chance to grow new skills and be part of a bold, collaborative, and inclusive culture where people can thrive and be at their best every day.</div><div>
We Are Challengers.</div><div>
We are dedicated to making self-care as simple as it should be. That starts with our culture. We are challengers by nature, and this is how we do things:</div><div>
All In Together: We keep each other honest and have each other's backs.</div><div>
Courageous: We break boundaries and take thoughtful risks with creativity.</div><div>
Outcome-Obsessed: We are personally accountable, driving sustainable impact and results with integrity.</div><div>
Radically Simple: We strive to make things simple for us and simple for consumers, as it should be.</div><div>
Join us on our mission. Health. In your hands.</div><div><div>
www.opella.com/en/careers</div></div></div>

Regulatory Data Model Governance Lead

<div></div><div><div>Job title: React.js Frontend Visualization Developer</div><ul><li>
Location: Hyderabad</li></ul><div></div><div>
Opella is the self-care challenger with the purest and third-largest portfolio in the Over-The-Counter (OTC) &amp; Vitamins, Minerals &amp; Supplements (VMS) market globally.</div><div>
Our mission is to bring health in people&rsquo;s hands by making self-care as simple as it should be. For half a billion consumers worldwide &ndash; and counting.</div><div>
At the core of this mission is our 100 loved brands, our 11,000-strong global team, our 13 best-in-class manufacturing sites and 4 specialized science and innovation development centers. Headquartered in France, Opella is the proud maker of many of the world&rsquo;s most loved brands, including Allegra, Buscopan, Doliprane, Dulcolax, Enterogermina, Essentiale and Mucosolvan.</div><div>
As a globally certified B Corp company, we are active players in the journey towards healthier people and planet. Find out more about our mission at <div>www.opella.com</div>.</div><div><i><br>
About the job:</i></div><div>
We are looking for a React.js Frontend Visualization Developer to help design, build, and integrate data-rich user interfaces for Opella&rsquo;s modern data products and decision intelligence platforms.<br>
<br>
This role will collaborate closely with visualization leads, product managers, data engineers, and backend teams to create seamless and dynamic front-end interfaces that bring insights to life&mdash;embedded within React.js applications that support self-service, enterprise-grade analytics experiences.<br>
<br>
You will also help implement data-driven UI components, dynamic filters, dashboards, and reusable layout systems that integrate with APIs, embedded analytics tools (e.g., Power BI/Looker/Tableau if applicable), and design systems aligned to our brand.</div><div><i><br>
Main responsibilities:</i></div><ul><li>Build and maintain modular, performant React.js components for embedding interactive visualizations and data applications</li><li>Work with product and design teams to translate complex data requirements into intuitive front-end workflows</li><li>Develop UI layers that connect to back-end APIs, embedded BI reports, or internal visualization frameworks</li><li>Collaborate with Power BI or backend engineers to embed reports/dashboards using REST APIs or JavaScript SDKs</li><li>Apply custom styling and theming using CSS/SASS and design tokens to match enterprise visual standards</li><li>Create responsive interfaces and stateful components using React Hooks or Context API</li><li>Contribute to reusable design systems, internal component libraries, and analytics UX guidelines</li><li>Optimize performance and load times, especially for embedded charts and large-scale UI rendering</li><li>Conduct testing, code reviews, and participate in agile development cycles</li><li>Support integration of role-based access, filters, and drill-down actions in embedded visual apps</li></ul><div><br>
Nice to Have<br>
<ul><li>Exposure to Power BI embedding with REST API or JavaScript SDK</li><li>Familiarity with D3.js, Recharts, Plotly, or other front-end charting libraries</li><li>Experience with enterprise BI tools (Power BI, Looker, Tableau)</li><li>Knowledge of authentication patterns (OAuth, Azure AD) in embedding contexts</li><li>Experience working alongside Snowflake, Databricks, or similar cloud data stacks</li><li>Familiarity with data governance, privacy, or analytics use cases in regulated industries (e.g., GxP, SOX)</li></ul></div><div><i><br>
About you:</i><br>
 &bull; 3+ years of experience building modern web applications with React.js<br>
<ul><li>Strong proficiency in JavaScript (ES6+), HTML5, CSS3, and component-based architecture</li><li>Experience with CSS customization, design systems, and styling libraries (Tailwind, styled-components, etc.)</li><li>Proficient in using React Hooks, Context, and component lifecycle patterns</li><li>Experience integrating with APIs (REST/GraphQL) to drive data visual elements</li><li>Familiarity with embedding analytics dashboards (e.g., Power BI, Tableau, or Looker) via JavaScript SDKs or iFrames</li><li>Ability to work with large JSON data structures and dynamic UI rendering</li><li>Solid understanding of responsive design, cross-browser compatibility, and performance optimization</li><li>Strong communication and collaboration skills within agile, cross-functional teams</li></ul></div><div><i><br>
Why us?</i></div><div></div><div>
At Opella, you will enjoy doing challenging, purposeful work, empowered to develop consumer brands with passion and creativity. This is your chance to grow new skills and be part of a bold, collaborative, and inclusive culture where people can thrive and be at their best every day.</div><div>
We Are Challengers.</div><div>
We are dedicated to making self-care as simple as it should be. That starts with our culture. We are challengers by nature, and this is how we do things:</div><div>
All In Together: We keep each other honest and have each other's backs.</div><div>
Courageous: We break boundaries and take thoughtful risks with creativity.</div><div>
Outcome-Obsessed: We are personally accountable, driving sustainable impact and results with integrity.</div><div>
Radically Simple: We strive to make things simple for us and simple for consumers, as it should be.</div><div>
Join us on our mission. Health. In your hands.</div><div><div>
www.opella.com/en/careers</div></div></div><div></div>

React.js Frontend Visualization Developer

<div><div>Opella is the self-care challenger with the purest and third-largest portfolio in the Over-The-Counter (OTC) &amp; Vitamins, Minerals &amp; Supplements (VMS) market globally.</div><div></div><div>
Our mission is to bring health in people&rsquo;s hands by making self-care as simple as it should be. For half a billion consumers worldwide &ndash; and counting.</div><div>
At the core of this mission is our 100 loved brands, our 11,000-strong global team, our 13 best-in-class manufacturing sites and 4 specialized science and innovation development centers. Headquartered in France, Opella is the proud maker of many of the world&rsquo;s most loved brands, including Allegra, Buscopan, Doliprane, Dulcolax, Enterogermina, Essentiale and Mucosolvan.</div><div></div><div>
As a globally certified B Corp company, we are active players in the journey towards healthier people and planet. Find out more about our mission at <div>www.opella.com</div>.</div><div></div><div>
About the job:</div><div></div><div>
As an Infrastructure and Quality Digital Analyst, you will be part of the Opella Digital Manufacturing and Supply North America organization. Our team supports manufacturing and supply operations in Chattanooga and partners with global colleagues in the Opella M&amp;S and Digital organizations.</div><div>
We focus on enabling and maintaining digital solutions that support infrastructure, compliance, and operational excellence. This includes a diverse portfolio of applications and systems that must be effectively integrated with business functions and external partners to ensure efficient and secure logistics and manufacturing operations.</div><div></div><div>
In this role, you will contribute to the support of infrastructure and applications related to Chromatography systems (e.g., Agilent Open Lab), Stability systems (e.g., Novatek), and various laboratory and manufacturing instruments. You&rsquo;ll gain hands-on experience while working alongside experienced professionals in a collaborative and learning-focused environment.</div><div></div><div>
Main responsibilities:</div><div></div><div>
Infrastructure &amp; Application Support:</div><ul><li><div>
Assist in maintaining infrastructure for lab and manufacturing systems.</div></li></ul><ul><li><div>
Support deployment and documentation of on-site infrastructure.</div></li></ul><ul><li><div>
Help monitor system performance and contribute to troubleshooting efforts.</div></li></ul><div></div><div>
Cybersecurity &amp; Compliance:</div><ul><li><div>
Learn and apply basic cybersecurity practices to protect systems.</div></li></ul><ul><li><div>
Support patching and updates for devices and applications.</div></li></ul><ul><li><div>
Assist in maintaining compliance with regulatory standards (e.g., CFR Part 11, GxP).</div></li></ul><div></div><div>
Collaboration &amp; Communication:</div><ul><li><div>
Work with cross-functional teams including automation, cybersecurity, and quality.</div></li></ul><ul><li><div>
Participate in meetings and contribute to project planning and execution.</div></li></ul><ul><li><div>
Serve as a liaison between site teams and global support functions.</div></li></ul><div></div><div>
Special Projects</div><ul><li><div>
Participate in cross-functional initiatives aimed at improving infrastructure efficiency, digital integration, and system reliability.</div></li></ul><ul><li><div>
Support pilot programs and proof-of-concept deployments for new technologies or process improvements.</div></li></ul><ul><li><div>
Contribute to documentation and knowledge sharing for lessons learned and best practices.</div></li></ul><div></div><div>
Operational Support:</div><ul><li><div>
Help manage peripherals such as tablets, printers, and scan guns.</div></li></ul><ul><li><div>
Support imaging and setup of non-standard desktops and laptops.</div></li></ul><ul><li><div>
Assist in maintaining inventory of GxP-compliant systems.</div></li></ul><div></div><div><i>
About you</i></div><div></div><div>
Education/Experience:</div><ul><li><div>
High School Diploma Reqired</div></li></ul><ul><li><div>
CompTIA Network+, Microsoft Certified: Azure Fundamentals, or similar certifications.</div></li></ul><ul><li><div>
Internship or hands-on lab experience in a network or systems support role.</div></li></ul><ul><li><div>
More than 2 years of relevant experience, on Infrastructure build project and operation, preferably in healthcare/ pharmaceutical industry.</div></li></ul><ul><li><div>
Experience on computerized systems validation/ infrastructure validation/ laboratory or CFR Part 11, GxP / SCADA systems (IoT or IIOT solutions).</div></li></ul><div></div><div>
Soft skills:</div><ul><li><div>
Strong problem-solving and analytical thinking.</div></li></ul><ul><li><div>
Excellent verbal and written communication skills.</div></li></ul><ul><li><div>
Ability to work independently and collaboratively in a team environment.</div></li></ul><ul><li><div>
Detail-oriented with strong organizational and documentation abilities.</div></li></ul><ul><li><div>
Eagerness to learn new technologies and adapt in a fast-paced setting.</div></li></ul><ul><li><div>
Professional demeanor with the ability to interact with cross-functional teams and stakeholders.</div></li></ul><div></div><div>
Technical skills:</div><ul><li><div>
Basic understanding of TCP/IP networking and protocols (DNS, DHCP, HTTP/S).</div></li></ul><ul><li><div>
Familiarity with PowerShell scripting for automation tasks.</div></li></ul><ul><li><div>
Knowledge of virtualization technologies (VMware, Hyper-V).</div></li></ul><ul><li><div>
Experience with Active Directory (user/group management, OU structure).</div></li></ul><ul><li><div>
Exposure to cybersecurity principles and compliance frameworks (e.g., GxP, CFR Part 11).</div></li></ul><ul><li><div>
Understanding of IT hardware including servers, desktops, and peripherals.
</div></li></ul><div></div><div>Why us?</div><div></div><div>
At Opella, you will enjoy doing challenging, purposeful work, empowered to develop consumer brands with passion and creativity. This is your chance to grow new skills and be part of a bold, collaborative, and inclusive culture where people can thrive and be at their best every day.</div><div></div><div>
We Are Challengers.</div><div>
We are dedicated to making self-care as simple as it should be. That starts with our culture. We are challengers by nature, and this is how we do things:</div><div></div><div>
All In Together: We keep each other honest and have each other's backs.</div><div>
Courageous: We break boundaries and take thoughtful risks with creativity.</div><div>
Outcome-Obsessed: We are personally accountable, driving sustainable impact and results with integrity.</div><div>
Radically Simple: We strive to make things simple for us and simple for consumers, as it should be.</div><div></div><div>
Join us on our mission. Health. In your hands.</div><div><div>
www.opella.com/en/careers</div></div></div>

Infrastructure and Quality Digital Analyst

<div><div>Job title: Study Safety Reporting Manager</div><ul><li>
Location: Hyderabad</li></ul><div></div><div>
Opella is the self-care challenger with the purest and third-largest portfolio in the Over-The-Counter (OTC) &amp; Vitamins, Minerals &amp; Supplements (VMS) market globally.
</div><div>Our mission: to bring health in people&rsquo;s hands by making self-care as simple as it should be for over half a billion consumers worldwide.
</div><div>At the core of this mission is our 100+ loved brands, our 11,000-strong global team, our 13 best-in-class manufacturing sites and four specialized science and innovation development centers.
</div><div>Headquartered in France, Opella is the proud maker of many of the world&rsquo;s most loved brands, including Allegra, Buscopan, Doliprane, Dulcolax, Enterogermina, Essentiale and Mucosolvan.
</div><div>B Corp certified in multiple markets, we are active players in the journey towards healthier people and planet.
</div><div>Find out more about our mission to bring health in your hands at <div>www.opella.com.</div>
</div><div></div><div>About the job:</div><div>
Reporting to the Global Safety Operational Group Lead at the Science (COE) at Hyderabad and will be working closely with the other global stakeholders including Case Management Head &amp; PV Ops Head for other relevant regulatory reports from clinical trials and post-marketed studies.</div><div></div><div>
Main responsibilities:</div><ul><li>
This role is responsible to ensure patient safety data from clinical trials and post-marketed studies is accurately represented in regulatory reports.</li></ul><ul><li>
Build and maintain strong partnerships with cross-functional teams including Clinical Trial Leads, RWE Study Leads, Regulatory Affairs, Medical Affairs, and vendor organizations to support DSUR/SASR/PBRER/ACO requirements.</li></ul><ul><li>
Collaborate closely with PV Ops Head, Global Safety Officer, Periodic Report Authoring Team, and other global functions to support safety reporting and regulatory documentation.</li></ul><ul><li>
Validate study lists and generate high-quality cumulative clinical exposure data from CTMS and non-interventional studies for periodic safety reports.</li></ul><ul><li>
Maintain compliance with global PV regulations and define standards for safety reporting based on evolving Health Authority expectations.</li></ul><ul><li>
Ensure all relevant safety sections of the clinical study protocols, SAE forms, and eCRFs are aligned with Opella SOPs and global regulatory requirements.</li></ul><ul><li>
Access and manage ongoing study data from CRO repositories and CTMS, ensuring accurate safety data transfer and configuration in PV databases.</li></ul><ul><li>
Provide strategic guidance to transversal teams for complex safety data analysis and regulatory responses, including ad hoc Health Authority queries.</li></ul><ul><li>
Drive continuous process improvements to enhance compliance, quality, and operational efficiency.</li><li>
Support case medical evaluator participation in safety analysis, enabling early identification and management of potential safety issues.</li><li>
Support PV Ops function in the oversight of local, regional, corporate, and vendor safety reporting activities.</li></ul><ul><li>
Actively contribute to global PV initiatives and collaborate with the Global Safety Officer on clinical and post-marketing program documentation.</li></ul><div></div><div>
Latitude of Action:</div><ul><li>
Validate list of studies for periodic reports versus previous issue to ensure consistency before making them available to stakeholders on a SharePoint.</li></ul><ul><li>
Ensure complete safety datasets from all Consumer Healthcare studies (interventional/non-interventional) in agreed formats for ready inclusion into periodic safety reports or any other regulatory reports.</li></ul><ul><li>
Inform relevant stakeholders of planning of periodic safety reports and addendum to clinical overview for the products they are responsible for.</li></ul><ul><li>
Produce predefined list of studies required for the preparation of periodic safety and regulatory reports according to master planning table, or for ad hoc audits and inspections.</li></ul><ul><li>
Validate the list of studies for periodic reports versus previous periodic safety report to ensure consistency before making them available to stakeholders on a SharePoint.</li></ul><ul><li>
Determine whether new studies were started or completed since the previous periodic report.</li></ul><ul><li>
Maintain and ensure cumulative exposure based on either receipt of information from the contact person or after receipt of clinical study report information.</li></ul><ul><li>
Contribute to defined data remediation process for &ldquo;old&rdquo; products.</li></ul><ul><li>
For non-global studies contact, inquire about access to datasets or aggregated data: Depending on cumulative exposure accountability, transfer local study exposure information to Statistician and/or store the data to further prepare cumulative clinical exposure tables for products without global project team according to rules established in the data remediation plan This requires consolidating prospectively the historical list of studies in scope according to this plan that depends on the age of the product, the type of access to data, etc.</li></ul><ul><li>
Follow up on the receipt and verify the completeness of data of ongoing or completed studies during the reference period received from affiliates for local studies or other contact for studies not managed by the Opella clinical department.</li></ul><ul><li>
Track the assessment of the report in the &ldquo;disclaimer&rdquo; document tracker and/or remediation meeting minutes.</li></ul><ul><li>
Ensure new studies are configured into the Opella&rsquo;s PV Safety database.</li></ul><ul><li>
Provide support in maintaining the planning of the DSUR with the coordination of the clinical study teams, global regulatory teams, and countries.</li></ul><div></div><div>
Role Impact:</div><ul><li>
Responsible to maintain compliance with all applicable PV regulations from safety data reporting from clinical studies</li></ul><ul><li>
Define, establish, and maintain global standards and expectations for Safety reporting based on expertise and awareness of Health Authority regulations on a global basis.</li></ul><ul><li>
Responsible to access ongoing study data from CRO repositories and Opella CTMS and ensure safety data transfer in PV database at the end of the study.</li></ul><ul><li>
This individual must provide direction and guidance to transversal teams in developing the complex analysis of clinical study and post-marketing data as well as in responding to Health Authorities.</li></ul><ul><li>
Responsible for implementing and maintaining the PSR-related tools and systems.</li></ul><ul><li>
Provide study-related information from Clinical Operations and Real-World Evidence for PV System Master File.</li></ul><ul><li>
Bring expertise for upgrade or development of new tools linked to CTMS or processes which identifies and monitors data quality and consistency.</li></ul><ul><li>
Support quality improvement projects through optimized processes, new technologies and innovation.</li></ul><div></div><div>
Scope:</div><ul><li>
The Study Safety Reporting Manager is responsible for ensuring accurate representation of patient safety data from clinical trials and post-marketed studies in regulatory reports.</li></ul><ul><li>
This role involves extensive cross-functional collaboration with internal and external stakeholders to manage study configurations, validate cumulative exposure data, and maintain compliance with global PV regulations.</li></ul><ul><li>
The individual also drives process improvements, oversees safety data integration from various sources, and provides strategic guidance for regulatory responses and safety surveillance activities.</li></ul><div></div><div>
About you:</div><div>
Qualifications:</div><ul><li>
Solid understanding of medical concepts and familiarity with safety activities in drug development and post-marketing and global safety health authority requirements.</li><li>
Experience working with global safety databases, including case management, periodic reports and comprehensive clinical data analysis.</li><li>
Author and/or process owner of controlled procedural documents (i.e., SOPs, Master Templates, Technical Documents, etc.).</li><li>
Solid knowledge of GCP, ICH and Global regulations.</li><li>
Inspection and audit support, including readiness activities</li><li>
Strong project management experience; ideally including having led outsourcing initiatives.</li><li>
Extensive experience leading compliance and quality management activities.</li><li>
Extensive knowledge and experience in leading transversal teams in formulating and writing Health Authority Responses.</li><li>
Demonstrated success in partnering and influencing across a matrix environment with exceptional executive communication skills.</li><li>
In depth understanding of data and the application of a variety of analytical techniques to derive insights from a set of objective and subjective data inputs.</li><li>
Pharmaceutical industry experience, especially in pharmacovigilance safety reports area</li><li>
Capability to organize and multitask activities, effectively prioritize and allocate resources</li><li>
Computer literacy especially in Windows based programs</li><li>
Ability to solve problems, to take initiative, to meet challenges, negotiation skills</li><li>
Fluent spoken and written English.</li><li>
Excellent written and oral communication skills</li><li>
Ability to effectively work with others throughout the organization, primarily affiliates/Country PV organization</li><li>
Fluent spoken and written English.</li></ul><div></div><div>
Preferred Qualifications:</div><ul><li>
Master&rsquo;s degree in pharmacy/Life sciences or HCPs with a minimum of 8-10 years of pharmacovigilance safety reporting handling of ICSRs &amp; Periodic Reports from both clinical trials and post-marketed studies.</li><li>
Any additional experience in consumer healthcare portfolio and cosmetic products would be an added advantage.</li></ul><div></div><div>
Why us?</div><div>
At Opella, you will enjoy doing challenging, purposeful work, empowered to develop consumer brands with passion and creativity. This is your chance to grow new skills and be part of a bold, collaborative, and inclusive culture where people can thrive and be at their best every day.</div><div></div><div>
We Are Challengers.</div><div>
We are dedicated to making self-care as simple as it should be. That starts with our culture. We are challengers by nature, and this is how we do things:</div><div></div><div>
All In Together: We keep each other honest and have each other's backs.</div><div>
Courageous: We break boundaries and take thoughtful risks with creativity.</div><div>
Outcome-Obsessed: We are personally accountable, driving sustainable impact and results with integrity.</div><div>
Radically Simple: We strive to make things simple for us and simple for consumers, as it should be.</div><div></div><div>
Join us on our mission. Health. In your hands.</div><div><div>
www.opella.com/en/careers</div></div></div>

Study Safety Reporting Manager

<div>
 <strong>
  About Us
  <br/>
  <br/>
 </strong>
 At Opella Healthcare, we are united by one shared Mission &ndash; we work passionately every day, to put Health in Your Hands. We are committed to making healthcare as simple as it should be, thus helping people help themselves. This Mission is the core of our philosophy, driving all that we do to focus on people&mdash;our consumers, customers, healthcare professionals, employees, and the Opella Brands that support them.
 <br/>
 <br/>
 As a top three global player in Consumer Healthcare, we are raising the bar with a bold ambition to grow, perform, and outpace the market. We aim to build a more agile and responsive organization capable of delivering our Vision and Mission.
 <br/>
 <br/>
 To achieve this, we need exceptional talent to shape Opella&rsquo;s future and help us succeed. Together, we embrace our Challenger spirit, driven by our commitment to be Outcome-obsessed, Courageous, Radically Simple, and All-In Together.
 <br/>
 <br/>
 <strong>
  Our Team
  <br/>
  <br/>
 </strong>
 The Opella Procurement External Manufacturing Team is part of the global Procurement. External Manufacturing Procurement ambition is to deliver Business Continuity with outstanding Value Creation. We are looking for a Regional Senior Buyer for the AMET cluster.
 <br/>
 <br/>
 <strong>
  Main Responsibilities
  <br/>
  <br/>
  Strategy
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Implement &amp; execute competitive and innovative Procurement Technology strategies for the full regional perimeter focused on FMCH:
  </li>
  <li>
  </li>
  <ul>
   <li>
    based on Procurement EM market intelligence: assessing risks and opportunities
   </li>
   <li>
    Budget &amp; Strategic Plan fully aligned with Business while delivering added value
   </li>
  </ul>
  <li>
   Deliver world class total savings objectives
  </li>
  <li>
   Contribute to the E2E make of buy strategy focusing on the AMET and AMEA brand needs on innovation &amp; localization to create value on FMCH KPIs
  </li>
  <li>
   Develop strong relationship with associated Procurement functions and Business Partners (IA &ndash; Global Growth Hub - Global Science Hub &ndash; Finance &ndash; Supply Chain &ndash; BD&amp;L)
  </li>
  <li>
   Define, implement, and monitor performance KPIs to meet the core needs of FMCH (innovation, supply securization, agile supply)
  </li>
  <li>
   Drive the development of new market opportunities (new suppliers, technologies, substitution products, etc.) aligned with the Procurement EM intelligence and category strategy
  </li>
  <li>
   Integrate sustainability into projects and business decisions to meet the EM sustainability roadmap
  </li>
  <li>
   Implement and execute e2e procurement relevant strategy to support CHC brands growth and gross margin
  </li>
  <li>
   Ensure Procurement technical excellence (TCO, SRM, Risk Management, CSR, HSE, compliance, quality&hellip;)
   <br/>
  </li>
 </ul>
 <strong>
  Contract &amp; Relationship Management
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Scout for a sustainable and value adding CDMO panel for AMET &amp; AMEA on FMCH
  </li>
  <li>
   Lead negotiations for her/his portfolio of CMOs
  </li>
  <li>
   Ensure compliance with master service agreements and/or specific contracts in place
  </li>
  <li>
   Ensure that terms and conditions of master service agreements and/or specific contracts,
  </li>
  <li>
   including the Quality Technical agreement (QTA) and sustainability requirements (BCorp) are met by all parties in the contract
  </li>
  <li>
   Monitor the contract life cycle and proactively manage negotiation phases with involved operational teams (i) in the set-up of a contract or (ii) request of quotation (RFQ) related to the supplier panel
  </li>
  <li>
   Ensure that risk management assessment and risk mitigation strategies are in place in close collaboration with the Business
  </li>
  <li>
   Set-Up and Lead Supplier Relationship Management (SRM) program for the key CMOs for her/his panel.
  </li>
  <li>
   Coordinate vendor innovation management
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Business Collaboration &amp; Partnering
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Build and ensure collaborative Business Partnering across the Business Unit internally and across the Supplier/CMO network
  </li>
  <li>
   Build and maintain strong interfaces and collaborations with other departments like finance, legal, regulatory, business development, licensing, and alliances &amp; partnerships on top of main stakeholder management (Science HUB, IA, CSO, Growth Hub, Quality and Regulatory teams)
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Expected Education &amp; Competencies
  <br/>
  <br/>
 </strong>
 <strong>
  Education &amp; Experience
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s degree in Sciences, Engineering or Business or another relevant field. An MBA preferred.
  </li>
  <li>
   At least 10 years&rsquo; experience in a Procurement role with proven record in term of change management and result delivery - plus experience in Consumer Health Care or FMCG
  </li>
  <li>
   Solid understanding of both Procurement and Operations; a combination of functional experiences in both Manufacturing and SCM as well as Procurement would be ideal.
  </li>
  <li>
   Experience in market intelligence
  </li>
  <li>
   Experience in implementing Procurement systems (SAP, Ariba, etc.) including design &amp; deployment is a benefit.
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Language &amp; Cultural
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Fluent in English and Arabic
  </li>
  <li>
   Plus: French and any other language
  </li>
  <li>
   International and multi-cultural mindset
  </li>
  <li>
   Strong change agent mindset
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  About You
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Leadership skills/experience with proven track record in building and leading cross functional teams
  </li>
  <li>
   Strong capability to manage business and interact with executive level: internal stakeholders, Suppliers and complex environment driven by a transformation thirst and acumen
  </li>
  <li>
   Sound track record in scouting for FMCH CDMOs
  </li>
  <li>
   Experience in agile partnerships on FMCH
  </li>
  <li>
   Skills and experience on sustainability projects (Ecovadis, FSC)
  </li>
  <li>
   Solid understanding in Cost management, budgeting and controlling - ability to understand and explain an Industrial P&amp;L to pilot financial performance
  </li>
  <li>
   Highly effective communication &amp; leadership skills to engage / motivate / influence teams
  </li>
  <li>
   Pragmatic problem-solving and proven decision-making skills with a continuous improvement mind-set
  </li>
  <li>
   Strong business acumen and ability to build sustainable business connectivity with strategic thinking
  </li>
  <li>
   Resilience and change agent
  </li>
  <li>
   Capability to manage business at executive level: internal stakeholders and suppliers
  </li>
  <li>
   Prioritization skills
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Why us?
  <br/>
  <br/>
 </strong>
 At Opella, you will enjoy doing challenging, purposeful work, empowered to develop consumer brands with passion and creativity. This is your chance to grow new skills and be part of a bold, collaborative, and inclusive culture where people can thrive and be at their best every day.
 <br/>
 <br/>
 <strong>
  We Are Challengers.
  <br/>
  <br/>
 </strong>
 We Are Dedicated To Making Self-care As Simple As It Should Be. That Starts With Our Culture. We Are Challengers By Nature, And This Is How We Do Things
 <br/>
 <br/>
 <strong>
  All In Together:
 </strong>
 We keep each other honest and have each other's backs.
 <br/>
 <br/>
 <strong>
  Courageous:
 </strong>
 We break boundaries and take thoughtful risks with creativity.
 <br/>
 <br/>
 <strong>
  Outcome-Obsessed:
 </strong>
 We are personally accountable, driving sustainable impact and results with integrity.
 <br/>
 <br/>
 <strong>
  Radically Simple:
 </strong>
 We strive to make things simple for us and simple for consumers, as it should be.
 <br/>
 <br/>
 Join us on our mission. Health. In your hands.
</div>


Regional Senior Buyer, AMET

<div>
 At Opella Healthcare, we are united by one shared
 <strong>
  Mission
 </strong>
 &ndash; we work passionately every day, to put
 <strong>
  Health in Your Hands
 </strong>
 . We are committed to making healthcare as simple as it should be, thus helping people help themselves. This Mission is the core of our philosophy, driving all that we do to focus on people&mdash;our consumers, customers, healthcare professionals, employees, and the Opella Brands that support them.
 <br/>
 <br/>
 As a top three global player in Consumer Healthcare, we are raising the bar with a bold ambition to grow, perform, and outpace the market. We aim to build a more agile and responsive organization capable of delivering our Vision and Mission.
 <br/>
 <br/>
 To achieve this, we need exceptional talent to shape Opella&rsquo;s future and help us succeed. Together, we embrace our Challenger spirit, driven by our commitment to be Outcome-obsessed, Courageous, Radically Simple, and All-In Together.
 <br/>
 <br/>
 <strong>
  Job Purpose
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Managing the Sales &amp; Operations Planning Process
  </li>
  <li>
   Coordinating the Supply Planning and Inventory Control activities
  </li>
  <li>
   Managing Drop and export shipments to Sudan
  </li>
  <li>
   Product Launch Coordination
  </li>
  <li>
   Coordinating Overprinting &amp; MOH release activities
  </li>
  <li>
   Product Master Data Management
  </li>
  <li>
   Management of Customs Clearance Process; 3PL agents and activity
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Key Results/Accountabilities
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Managing the SOP meetings and recording Forecast Review minutes and actions and ensuring timely forecast update on SC systems
  </li>
  <li>
   Coordination with plants and SC Hub for supply planning &amp; shipments organization
  </li>
  <li>
   Liaise with Treasury Teams for fx requirement
  </li>
  <li>
   Monitoring and maintaining Egypt&rsquo;s inventory levels between agreed minimum and maximum levels, reducing the level of stock write offs due to redundancy.
  </li>
  <li>
   Assist the BU with planning and ensuring timeous new product launches
  </li>
  <li>
   Coordinating the overprinting &amp; MOH release activities with DRA and DC teams
  </li>
  <li>
   Customs Clearance Activity and management of forwarding agents
  </li>
  <li>
   Liaise with Sudan management and Sudanese agents for orders production and shipment
  </li>
  <li>
   Monthly TM alignment and Sales In realization for Sudan
  </li>
  <li>
   Coordinating the flow of Drop Shipments to Sudan
  </li>
  <li>
   Managing the export flow documentation to Sudan
  </li>
  <li>
   Regular maintenance of master data files on all SC tools and resolving interface issues
  </li>
  <li>
   Coordinating regulatory variations and implementing mitigating plans to avoid supply shortfalls
  </li>
  <li>
   Ensure proper and timeous communication to BU&rsquo;s regarding product alerts and mitigation plans
  </li>
  <li>
   Assist on finalizing all Chloe project aspects, with cross functional teams to ensure successful operation on Chloe Day
  </li>
  <li>
   Ad hoc projects &amp; Tasks
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  <strong>
   KEY WORKING RELATIONSHIPS
   <br/>
   <br/>
  </strong>
 </strong>
 <ul>
  <li>
   Sales &amp; Marketing Teams
  </li>
  <li>
   Finance BP
  </li>
  <li>
   Global Plants and DCs
  </li>
  <li>
   COE Team in Barcelona
  </li>
  <li>
   3rd Party Logistics Providers
  </li>
  <li>
   Sudan Management &amp; Sudanese Agents
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Skills, Experience &amp; Knowledge Requirements
  <br/>
  <br/>
 </strong>
 <strong>
  Education and Experience:
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Bachelor&rsquo;s degree in accounting or business administration
  </li>
  <li>
   3 years&rsquo; experience in Demand and Inventory Management in the CHC / FMCG Sector
  </li>
  <li>
   Must be able to operate transversely and have good communication skills
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Knowledge
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Excellent computer skills (MS office, Outlook &amp; SAP)
  </li>
  <li>
   Key aspects of the pharma industry
  </li>
  <li>
   Distribution procedures
  </li>
  <li>
   Customer groups within Pharmaceutical Industry
  </li>
  <li>
   Distribution channels
  </li>
  <li>
   Understanding of Single Exit Pricing
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  Language &amp; Cultural
  <br/>
  <br/>
 </strong>
 <ul>
  <li>
   Fluent in English and Arabic
  </li>
  <li>
   Plus: French and any other language
  </li>
  <li>
   International and multi-cultural mindset
  </li>
  <li>
   Strong change agent mindset
   <br/>
   <br/>
  </li>
 </ul>
 <strong>
  WHY US?
  <br/>
  <br/>
 </strong>
 At Opella, you will enjoy doing challenging, purposeful work, empowered to develop consumer brands with passion and creativity. This is your chance to grow new skills and be part of a bold, collaborative, and inclusive culture where people can thrive and be at their best every day.
 <br/>
 <br/>
 <strong>
  We Are Challengers.
  <br/>
  <br/>
 </strong>
 We Are Dedicated To Making Self-care As Simple As It Should Be. That Starts With Our Culture. We Are Challengers By Nature, And This Is How We Do Things
 <br/>
 <br/>
 <strong>
  All In Together:
 </strong>
 We keep each other honest and have each other's backs.
 <br/>
 <br/>
 <strong>
  Courageous:
 </strong>
 We break boundaries and take thoughtful risks with creativity.
 <br/>
 <br/>
 <strong>
  Outcome-Obsessed:
 </strong>
 We are personally accountable, driving sustainable impact and results with integrity.
 <br/>
 <br/>
 <strong>
  Radically Simple:
 </strong>
 We strive to make things simple for us and simple for consumers, as it should be.
 <br/>
 <br/>
 Join us on our mission. Health. In your hands.
 <br/>
 <br/>
 www.opella.com/en/careers
</div>


Integrated Business Planning Lead

<div><div>Job title: Ecommerce media specialist,</div><ul><li>
Location: Hyderabad</li></ul><div></div><div>
Opella is the self-care challenger with the purest and third-largest portfolio in the Over-The-Counter (OTC) &amp; Vitamins, Minerals &amp; Supplements (VMS) market globally.
</div><div>Our mission: to bring health in people&rsquo;s hands by making self-care as simple as it should be for over half a billion consumers worldwide.
</div><div>At the core of this mission is our 100+ loved brands, our 11,000-strong global team, our 13 best-in-class manufacturing sites and four specialized science and innovation development centers.
</div><div>Headquartered in France, Opella is the proud maker of many of the world&rsquo;s most loved brands, including Allegra, Buscopan, Doliprane, Dulcolax, Enterogermina, Essentiale and Mucosolvan.
</div><div>B Corp certified in multiple markets, we are active players in the journey towards healthier people and planet.
</div><div>Find out more about our mission to bring health in your hands at <div>www.opella.com.</div></div><div></div><div>
About the job:</div><div>
The ecommerce media specialist will be responsible for executing day-to-day operations related to ecommerce paid Search on eRetailer platforms. This includes bidding, dashboarding, and ensuring the successful implementation of campaigns under the guidance of the eCommerce Operations Director.</div><div></div><div>
Main responsibilities:</div><ul><li>
Create, monitor, and optimize advertising campaigns.</li><li>
Use bidding tool custom rules and automated bidding strategies, algorithms, A/B tests capabilities to optimize and monitor performance.</li><li>
Employ keyword research tools and analytics platforms to refine campaign targeting and optimize keyword selection.</li><li>
Leverage machine learning models to derive actionable insights from campaign data, informing strategic optimizations.</li><li>
Collect campaigns data and create reports.</li></ul><div></div><div>
About you:</div><div>
Qualifications</div><ul><li>
Hands on keyboard experience in buying eCommerce media (on platforms such as Amazon Ads, Skai or Pacvue)</li><li>
Strong understanding of CPG specificities (category management)</li><li>
Detail-oriented with strong analytical skills.</li><li>
Effective communication written and oral in English and teamwork abilities.</li><li>
Excellent communication and collaboration skills as well as proficiency in data analysis and reporting tools.</li></ul><div></div><div>
Experience</div><ul><li>
Significant experience in the digital media space: in media agency or trading desk - including on Amazon search Ads</li></ul><div></div><div>
Why us?</div><div></div><div>
At Opella, you will enjoy doing challenging, purposeful work, empowered to develop consumer brands with passion and creativity. This is your chance to grow new skills and be part of a bold, collaborative, and inclusive culture where people can thrive and be at their best every day.</div><div></div><div>
We Are Challengers.</div><div>
We are dedicated to making self-care as simple as it should be. That starts with our culture. We are challengers by nature, and this is how we do things:</div><div></div><div>
All In Together: We keep each other honest and have each other's backs.</div><div>
Courageous: We break boundaries and take thoughtful risks with creativity.</div><div>
Outcome-Obsessed: We are personally accountable, driving sustainable impact and results with integrity.</div><div>
Radically Simple: We strive to make things simple for us and simple for consumers, as it should be.</div><div></div><div>
Join us on our mission. Health. In your hands.</div><div><div>
www.opella.com/en/careers</div></div></div><div></div>

eCommerce media specialist

Join Opella and explore 13   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.