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Position part of the procurement team focused in improving and re-evaluating the procurement activities, optimizing the organization's supply base and increasing its overall value proposition. Focused on the total cost of ownership, this position also considers product quality, customer needs, organizational goals and market conditions as an essential part of the procurement process. Actions are driven by a rigorous and collaborative approach, based on fact analysis and market intelligence, following the Strategic Sourcing Framework. Ensure the availability of raw material, both; short and long term, through regular monitorization of critical raw materials and a continuous analysis of risks to define risk mitigation actions. Regular reporting and analysis of the main purchasing KPIs, such as • Obsolescence Main responsible for the price negotiation and the management of materials savings initiatives in line with profit plan and overall business objectives. Negotiation of supply agreements as needed to support the critical business needs: • Monitorization and renewal of existing Supply and Quality Agreements, • Ensures Supply and Quality Agreements are positioned appropriately before business is initiated with new vendors Improve the value-to-price relationship with suppliers following Strategic Sourcing Framework • Quarterly communication of raw material forecast, • Follow up calls with all the vendors, • Annual visit plan with key vendors, • Attendance to main exhibitions Supports Supplier Quality department to accomplish the goals defined in supplier quality system • Annual risk analysis of raw materials and definition of key vendors list, • Analysis of vendors performance Ensure the maximum quality of the purchased products • Follow up of technical problems with Supplier Quality, Technical Support, R&Dor Manufacturing departments Contribute to keep updated the material and supplier database Strategic activities • Development and implementation of the Strategic Sourcing strategy, • Develop key performance measures for chosen suppliers and negotiate on multiple variables to award longer-term strategic contracts that result in significant cost reduction and improved service levels, • Monitor current category market conditions, technology roadmaps and identify supply/demand challenges & opportunities., • Identification of new suppliers in collaboration with R&D during the development of new products, • Identification of potential risk and definition of mitigation action plans, • Involvement in the total cost analysis for new product developments To be determined based on department needs, to include interactions such as: • Supplier Quality: Control change notification management and vendor's complaints support, • Manufacturing: Support in solving technical issues related to raw material or packaging performance, • R&D: Support in the development of new products and identifying suppliers for new assays, • Supply Chain Department; Including warehouse and planning, • Sales and Marketing: Benchmarking of vendors, • Quality Control The ideal candidate for this position will exhibit the following skills and competencies: • Management of decisions under pressure., • Methodical and well-organized person., • Teamwork, • Ability to express information clearly and concisely to the staff, ensuring their understanding., • Ability to apply a systematic approach and constant control, follow-up and verification of the results., • Ability to collaborate, participate and coordinate actively with working groups, • Good reporting and analysis capabilities, • Reflects values of Werfen in the quality of work and working relationship. Education: • Required: Bachelor's degree (Diplomatura) in the biological or related sciences. Degree may be substituted by relevant skills and work experience, • Valuable: Any additional degree higher than the required Experience: • Professional experience is required, minimum of 5 years in a similar position, • Software: Fluency in Office Tools (Excel & Word), Valuable advanced knowledge in SAP, • Language: Fluency in Spanish or Catalan. Advanced knowledge of English (reading, writing and speaking) Additional Skills/Knowledge: • Software: Fluency in Office Tools (Excel & Word), Valuable Advanced knowledge in SAP, • Language: Fluency in Spanish or Catalan. Medium knowledge of English reading, writing and speaking) #J-18808-Ljbffr

Actual Talent is a talent acquisition consultancy that offers Executive Search, RPO and Talent Solutions. Our purpose is to drive the growth and fulfillment of individuals and organizations. We facilitate individuals in finding inspiring opportunities and help organizations discover professionals who will take them to the next level. We do this through talent acquisition and development solutions that focus on people, diversity and inclusion, innovation, and cutting-edge technology. A molecular diagnostics company established through a strategic partnership between two global leaders in the in vitro diagnostics and molecular testing industry. The company brings together advanced molecular diagnostics technology and extensive IVD expertise to develop innovative solutions for hospitals and laboratories, with a strong focus on advancing patient care worldwide. Reporting to R&D Director, this position performs a broad range of laboratory work requiring application of professional judgment in the selection of specialized methods and techniques, and their application to specific tasks. Provides project updates. Performs duties in research and development including the ability to perform specialized lab techniques and good laboratory documentation practices. • Performs an expanded range of laboratory procedures and experiments, • Periodically communicates problems, and progress to supervisor, • Occasionally communicates status updates and results across the organization, • Presents results to senior/other research staff, • Selects appropriate experimental and analytical methods and define protocols, • Schedules own and team tasks and activities in accordance with assignments and priorities, • Detects deviations in results and potential problems, recommends modification in protocols or standard methodology to define the causes of deviations and overcome problems, • Under the supervision and approval of his/her supervisor, writes specialized laboratory procedures and reviews existing Procedures and Methods, • Compiles and interprets experimental data, performs calculations and prepares graphs to present and discuss them to his/her supervisor, • Writes research papers, reports, reviews, and technical summaries, • Review electronic or paper laboratory notebook making sure that all data is accurately recorded in accordance with guidelines and procedures, • Required: Bachelor's degree (Licenciatura) in the Biological or related sciences plus extensive work experience., • Valuable: Any additional degree higher than that required in the previous section, • Required: Basic knowledge of biological and chemical laboratory procedures and ability to operate laboratory equipment, • Valuable: Knowledge of molecular biology techniques and experience in molecular diagnostic development, • Professional industrial experience in scientific or in vitro diagnostic research will be also valued, • Software: Proficiency in basic software tools (Excel, Word, PowerPoint). Knowledge of SAP preferred, • Language: Fluency in Spanish or Catalan. Advanced knowledge of English (reading, speaking and writing), • Able to use and apply general scientific methods, theories and concepts, • Teamwork and interpersonal skills. Flexibility in order to work with, and provide support for a number of people, • Oral and written communication skills, • Time management skills. Ability to priorize tasks and multi-tasking skills, • Well organized, able to handle large data sets, and communicate results, problems, and progress to the supervisor, and within the group as required, • Thorough knowledge of design control processes and familiarity with quality standards as required, • Ability to adapt to R&D flexible and changing environment, • Able to work independently on the project with moderate guidance, • Dynamic Environment: Collaborate with teams across departments, companies and countries to exceed customer expectations., • Global Impact: Contribute to the advancement of patient care worldwide through innovative specialized diagnostics., • An incredible work atmosphere and a broad range of social benefits including health insurance, canteen, retirement plan, and much more. #J-18808-Ljbffr

The position is responsible for ensuring that products developed by Biokit meet all Quality requirements and are documented in compliance with all applicable regulations. The position provides quality oversight for the development and commercialization of new assay products in addition to post commercialization design changes for assays. Provide Design Control / Design Change Control guidance to internal or external product development teams, including risk management and development of regulatory strategies and plans. The role will ensure that assay developed by Biokit in compliance with the Product Development process & Biokit Quality System and worldwide design control regulations. Key outputs include: documentation to support efficient worldwide regulatory submissions, product risk management, and comprehensive design history. Ensure effective partnering and collaboration with R&D, Quality Operations, Regulatory Affairs and Operations to meet project goals, maintain compliance, and complete defined regulatory submissions. Partner with the R&D teams ensuring a risk-based approach to the validation and implementation of product changes to existing products while maintaining compliance with Quality System elements, including but not limited to: Design Control, Design Change, Risk Management and Change Control. Provide Quality Oversight to non-conformance, root cause investigations and CAPA. Ensures that all documentation is QA reviewed before it is shared externally with regulators and/or customers. Lead activities to continuously improve DQ processes, standards, tools, and techniques to ensure they effectively and efficiently meet external standards. Designs and delivers appropriate training to develop the overall competency of the organization regarding design control. Collaborates with other QRA groups, R&D, and Operations to ensure successful Regulatory Inspections. To be determined based on department needs, to include interactions such as: Operations Area R&D Area Sales & Marketing Required: Bachelor's degree (Diplomatura) in Life Sciences, Engineering, or Physical Science. Degree may be substituted by relevant skills and work experience. Valuable: Any additional degree higher than that required previously. Minimum of 3 years in a similar position. Software: Fluency in Office Tools (Excel & Word). Valuable: Basic knowledge in SAP. Language: Fluency in Spanish or Catalan. Advanced knowledge of English (reading and speaking). Standards: Knowledge of Quality standards, including design control and validation. Certifications include ASQ–CQA, ASQ-CQE, ASQ-SWQE, ASQCQM, Process Excellence. Management has the discretion of substituting relevant work experience for a degree and/or making exceptions to the years of experience requirement. The ideal candidate for this position will exhibit the following skills and capabilities: Management of decisions under pressure. Methodical and well-organized person. Teamwork. Time management skills. Ability to express information clearly and concisely to the staff, ensuring their understanding. Ability to apply a systematic approach and constant control, follow-up and verification of the results. Ability to collaborate, participate and coordinate actively with working groups. Reflects values of Werfen in the quality of work and working relationship. #J-18808-Ljbffr