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Who are we? We are TD SYNNEX, one of the world's leading technology distributors and solutions aggregators. We connect vendors, partners, and customers to make innovative technologies accessible and drive digital transformation globally. Our community of over 25,000 passionate professionals is committed to delivering products, services, and solutions that create real impact. We help organizations of all sizes maximize the value of their IT investments, achieve sustainable results, and unlock new growth opportunities. At the heart of everything we do is care-for our people, our partners, our customers, and the environment we share. We are dedicated to being a diverse, equitable, and inclusive organization and a responsible corporate citizen. And now... we are looking for a QEHS Specialist to join our team in Alovera and play a key role in ensuring compliance with Health & Safety, Quality, and Environmental standards across our operations! Job Purpose: Ensure compliance with Health & Safety, Quality, and Environmental regulations across TD SYNNEX sites in Alovera, driving continuous improvement. What You'll Do: • Implement and monitor Health & Safety management systems and policies across all levels., • Investigate accidents and incidents, reporting to official authorities., • Identify and assess workplace risks at TD SYNNEX facilities and external sites., • Coordinate mandatory Health & Safety training and awareness programs for Quality and Environment., • Stay updated on legislative changes and promote a strong safety culture., • Organize emergency drills and corrective actions., • Maintain environmental management system (KPIs, objectives, communication)., • Support ISO certifications (9001, 14001, 45001) and legal audits., • Manage supplier negotiations and purchase orders for Facilities. What We're Looking For: • Master's Degree in Prevención de Riesgos Laborales (Spain) with all three specializations., • 3-5 years of experience in Health & Safety, ideally in logistics/distribution., • Strong knowledge of Spanish H&S law and compliance., • Ability to lead, communicate, and manage multiple priorities., • Proficiency in MS Office and excellent organizational skills. If you are ready to join us as the QEHS Specialist - Health, Safety & Environment and play an instrumental role in shaping the future of technology solutions, apply now and take this amazing opportunity to make your mark in our organization. #LI-MM1 Key Skills At TD SYNNEX, our values guide everything we do: Together, We Own It, We Dare to Go, We Grow and Win, and above all, We Do the Right Thing. These principles shape how we work with each other, our partners, and our communities as we drive innovation and create lasting impact. What's In It For You? • Elective Benefits: Our programs are tailored to your country to best accommodate your lifestyle., • Grow Your Career: Accelerate your path to success (and keep up with the future) with formal programs on leadership and professional development, and many more on-demand courses., • Elevate Your Personal Well-Being: Boost your financial, physical, and mental well-being through seminars, events, and our global Life Empowerment Assistance Program., • Diversity, Equity & Inclusion: It's not just a phrase to us; valuing every voice is how we succeed. Join us in celebrating our global diversity through inclusive education, meaningful peer-to-peer conversations, and equitable growth and development opportunities., • Make the Most of our Global Organization: Network with other new co-workers within your first 30 days through our onboarding program., • Connect with Your Community: Participate in internal, peer-led inclusive communities and activities, including business resource groups, local volunteering events, and more environmental and social initiatives. Don't meet every single requirement? Apply anyway. At TD SYNNEX, we're proud to be recognized as a great place to work and a leader in the promotion and practice of diversity, equity and inclusion. If you're excited about working for our company and believe you're a good fit for this role, we encourage you to apply. You may be exactly the person we're looking for!

Want to join a company with a century-long tradition of innovation and entrepreneurial spirit that pushes the limits of the smart lighting industry? A company that requires employees to broaden their expertise to not only light urban environments but also deliver services for engaging and interactive public spaces. With a rich heritage in engineering, environmentally, economically, and socially sustainable lighting has always been part of our DNA. With connectivity more vital more ever, as Experts in Lightability™, we propose lighting infrastructure that will play a pivotal role in building Smart Cities. A family-owned Belgian company with headquarters in Brussels, we are present in over 70 countries on 5 continents. Will you take the challenge? Let’s light up the future together! Job Description • Manage Quality department, including Incoming Quality Inspection, In Process Quality Control & Finished Product Quality Inspection areas. Manage also Health, Safety & Environment topics. • Management of the Quality department and all the related elements, such as: incoming goods inspection, quality control during production and quality inspection of finished products., • Quality management also considers the product industrialization process (implementation of control plans, FMEA…), • Management of health, safety, and environmental topics (in connection with the ISO certification system and the local regulations)., • Management of relations with "internal customers" (commercial entities): complaints management, audits, visits. Main Purpose Of The Job • Take part in the product industrialization process (new developments, lifecycle and inter-factory product transfer), • Implement a clear and secure control plan, • Perform FMEA, • Manage both customer and supplier complaint handling processes., • Perform / give support to the team or to the Group Quality team on root cause analysis, • Keep contact with customers and suppliers, • Coordinate product certification (ENEC, ETL, ATEX / IECEx, EN40) related activities according to legal requirements, • Introduce and manage Integrated Management System according to ISO 9001, ISO 14001, OHSAS 18001, ISO 50001 standards, • Responsible of Health, Safety & Environment topics, • People management, • Local Quality team management with individual support for skills and career developmen., • In collaboration with the Plant manager, ensure that the factory’s overall activity complies with local legislation and regulation (work environment, products, structure…) Qualifications • Engineering Master Degree (mechanical / quality), • At least 5-10 years in a relevant position, • Experience in team management, • Languages : English (B2) + local language (Spanish), • Good knowledge of quality assurance methodologies (FMEA, SPC, PDCA, DMAIC, 6 Sigma, PQP), • Good communication skills, • Good analytical skills, • Rigorous & Assertive, • Internal audit certification (Quality, Environment, Health & Safety Management System) Additional Information Respect is one of our Values. Inclusivity is part of who we are, so we encourage applications from all backgrounds, communities and industries and are committed to having a team that is made up of diverse skills, experiences and abilities. At Schréder, we commit ourselves to co-creating an environment where passionate people work and win together, learn and have fun. Let Join us! We would like to hear from you if you have any feedback about our recruitment process. Please email us at . Respect is one of our Values. Inclusivity is part of who we are, so we encourage applications from all backgrounds, communities and industries and are committed to having a team that is made up of diverse skills, experiences and abilities.

Job Title: Warehouse Procurement Specialist (Spain) Location: Spain, Guadalajara Experience Level: 1-3 Years Position Summary The Warehouse Procurement Specialist will be responsible for sourcing, negotiating, and procuring a broad range of goods and services essential for the efficient operation of our warehouse facilities in Spain. This role is critical for ensuring cost efficiency, quality, and timely delivery of all necessary materials and services. Key Responsibilities Asset and Equipment Procurement: Purchase warehouse assets and equipment (e.g., shelving, MHE - Material Handling Equipment, IT hardware) in line with operational requirements and budget constraints. Consumables and Packaging: Manage the procurement of all packaging materials (boxes, tape, labels, etc.) and other essential operational consumables. Outsourcing and Services: Source and manage contracts for outsourced services, including but not limited to cleaning, security, maintenance, and other external service providers. Leasing and Facility Services: Handle the procurement related to facility leasing, equipment leasing, and general administrative services for the warehouse. Engineering and Projects: Support procurement activities for warehouse engineering projects, facility upgrades, and infrastructure maintenance. Vendor Management: Identify, evaluate, and onboard new vendors; manage and maintain strong, collaborative relationships with existing suppliers to ensure performance, quality, and cost-effectiveness. Negotiation and Cost Control: Conduct effective negotiations for contracts, pricing, and terms to achieve the best value for the company and drive cost savings. Documentation and Compliance: Ensure all procurement activities comply with company policies, local regulations, and maintain accurate records of purchases, contracts, and supplier performance. 职位描述 Requirements Experience: 1-3 years of proven working experience in Procurement, Sourcing, Supply Chain, or a related field, preferably within a logistics, warehouse, or e-commerce environment. Education: Bachelor's degree in Supply Chain Management, Business Administration, Logistics, or a related discipline. Language: Fluency in Chinese, Spanish is essential Skills: Strong negotiation and contracting skills. Excellent analytical and problem-solving abilities. Proficiency in Microsoft Office Suite (especially Excel) and experience with procurement software (e.g., ERP systems, e-Sourcing platforms). Detail-oriented and highly organized with the ability to manage multiple priorities simultaneously. Location: Must be legally eligible to work in Spain and be based locally.

In a nutshell Position: Pharmaceutical Development Manager - External Operations Location: Azuqueca de Henares Experience: More than 5 years in the development of the position and duties described Want to know more? INSUD PHARMA operates across the entire pharmaceutical value chain, providing expertise and experience in scientific research, development, manufacturing, sales and marketing of a wide range of active pharmaceutical ingredients (APIs), finished dosage forms (FDFs) and branded pharmaceutical products, with added value for human and animal health. INSUD PHARMA's activity is organised into three synergistic business areas: Industrial (Chemo), Branded (Exeltis) and Biotech (mAbxience), with more than 9,000 professionals in over 50 countries, 20 state-of-the-art facilities, 15 specialised R&D centres, 12 commercial offices and more than 35 pharmaceutical subsidiaries, serving 1,150 customers in 96 countries around the world. INSUD PHARMA believes in innovation and sustainable development. What are we looking for? We are recruiting a Pharmaceutical Development Manager – External Operations to join the R&D team at one of our plants located in Azuqueca de Henares. The challenge! As Pharmaceutical Development Manager - External Operations, you will lead, coordinate and supervise pharmaceutical development projects carried out at Insud Pharma Group's sites outside Spain and with external partners. Your mission: to ensure the highest quality development and smooth technology transfer of solid oral and semi-solid dosage forms from external centres to our flagship plant in Spain, driving the success of the portfolio in multiple markets. Specific responsibilities Provide strategic oversight of R&D projects developed at Insud Pharma Group plants outside Spain and through external partners such as CDMOs worldwide, primarily in solid oral and semi-solid dosage forms. Manage all formulation, analytical and process development activities, from pre-formulation to industrialisation, ensuring overall compliance with corporate objectives, regulatory requirements and project deadlines. Supervise, guide and inspire a high-performance team; define annual objectives aligned with the company's strategy and foster a culture of innovation, engagement and continuous improvement. Review, approve and validate project documentation (development, analytical, regulatory, clinical) prepared by international and third-party teams, ensuring the most rigorous standards for regulatory submission and audit readiness. Drive seamless technology transfer and product scaling, ensuring robust implementation in Spanish production (Liconsa), including plant preparation, process reproducibility, equipment qualification and comprehensive technical documentation. Align projects and coordinate effectively with global cross-functional teams: Clinical Development, Production, Regulatory Affairs, Business Development, Supply Chain, Quality, among others. Propose optimal resource allocation and lead change initiatives to enhance capacity, efficiency and adoption of best practices in internal and external networks. Monitor KPIs for deadline compliance, document quality, process reproducibility and submission/approval rates; proactively address project risks and leverage new opportunities. Present project status and strategic recommendations to senior management and global leadership, acting as a visible benchmark for external innovation, excellence, and patient-centred value. Support business audits, budget planning, and talent development; play a key role in organisational and cultural integration. What do you need? Higher degree in Pharmacy, Pharmaceutical Sciences, Chemistry or related field. ≥5 years of experience in pharmaceutical development, with proven experience in managing international projects and with third parties (/CDMOs); experience in generic drug development highly valued. Solid knowledge of formulation, analytical and process development—especially for solid and semi-solid oral forms; practical experience in scale-up, technology transfer and regulatory submissions (FDA/EMA and others) required. Fluency in English (spoken/written); Spanish and/or other languages will be a significant advantage. Proven leadership of multidisciplinary and multicultural teams; able to align diverse stakeholders in a highly dynamic and matrix environment. Excellent project management, negotiation, and interpersonal skills; proven track record in problem solving, innovation, and meeting objectives on time and within budget. Willingness to travel internationally to external sites and collaborating organisations as needed. Passion for quality, patient safety, and making a difference in global health. Our benefits! ⏰Monday to Friday working hours, with flexible start times between 8:00 a.m. and 9:30 a.m. and finish times depending on start time, from 4:30 p.m. onwards. Permanent contract. Attractive salary package. Life and accident insurance. Co-payment for voluntary health insurance. Benefits and Savings Club. Development plans, internal mobility policy. ⭐And much more! COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma group is aware that business management must be in line with the needs and demands of society, and therefore is committed to equal opportunities and treatment between men and women, as set out in current legislation on the matter -Organic Law 3/2007, and we do not discriminate against anyone on the basis of ethnicity, religion, age, sex, nationality, marital status, emotional or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

In short Position: Clinical Development Leader Location: Azuqueca de Henares. Experience: 3 to 5 years in similar roles. Want to know more? INSUD PHARMA operates across the entire pharmaceutical value chain, providing specialized knowledge and experience in scientific research, development, manufacturing, sales, and marketing of a wide range of active pharmaceutical ingredients (APIs), finished dosage forms (FDFs), and branded pharmaceutical products, adding value for human and animal health. INSUD PHARMA’s activity is organized into three synergistic business areas: Industrial (Chemo), Branded (Exeltis), and Biotech (mAbxience), with over 9,000 professionals in more than 50 countries, 20 state-of-the-art facilities, 15 specialized R&D centers, 12 commercial offices, and over 35 pharmaceutical subsidiaries, serving 1,150 clients in 96 countries worldwide. INSUD PHARMA believes in innovation and sustainable development. Ready to become a #Challenger? What are we looking for? Planning, designing, organization, supervision of conduct and reporting of clinical trial contracted to Clinical Research Organizations (CRO) to enable studies execution within the planned timelines and in compliance with current GCP and other applicable requirements. The main focus is on pharmacokinetic (PK) and bioequivalence (BE) trials. Multicenter clinical trials and phase II and III trials may also be required with the necessary support. The challenge! Assume overall responsibility for the plan, design, execution, reporting and evaluation of results of clinical trials as well as assure conduct of the trials in compliance with applicable requirements including but not limited to GCP. Specific responsibilities include: Design and manage the clinical trials according to plan and in compliance with applicable laws, regulations, and guidelines (ICH, EMA, FDA, and others). Participate in the selection of CROs and other external vendors and control the execution of all contracted activities and ensure that the activities are conducted in accordance with the requirements (cost, quality, and time). Review the necessary documentation before (e.g. Protocol, ICF, etc.), during (e.g. Monitoring etc.) and at the end (e.g. Study Report, etc.) of clinical trials. Coordinate internal Chemo activities and procedures related with the conduct of the clinical trials (e.g. investigational medication shipment, etc.). Collaborate in the interaction with Health Authorities: Scientific Advices and Deficiency Letters. Collaborate with other departments and experts (e.g. in Pharmaceutical Development, Regulatory, Pharmacovigilance, Project Management) to define strategies and plans for projects execution and execute clinical activities according to agreed plans. Participate on the maintenance of GCP system through elaboration and/or review of SOPs, etc. Contribute to the maintenance of GCP system through elaboration and/or review of SOPs, etc. Specific Knowledge: Experience in global Clinical Development, primarily in PK and BE studies: Current knowledge of laws, regulations, and guidance (ICH, EMA, FDA, etc.) related to design and execution of clinical trials, primarily PK and BE studies as well as demonstrating bioequivalence in general. Experience in studies design and studies program development. Preparation and review of study documentation. Implementation of trials in global environment: Site selection and management (clinical / bioanalytical sites, monitoring activities). Project management of multiple studies Experience in development of generic drugs and related methodologies: evaluation of in vitro dissolution studies results, evaluation of PK/BE studies results and reports, assessment of suitability of bioanalytical methods, in vitro/in vivo correlations etc. Experience (years/area): Mandatory: Degree in Medicine, Pharmacy or Life Science Desired: Training/experience in Pharmacokinetics, bioequivalence studies and most of the relevant guidelines. Fluent in English required, communicative level in Spanish preferred, knowledge of other languages will be an asset. At least 3 years of experience in a similar position. Our Benefits! ⏰Flexible start hours from Monday to Friday (full 40-hour workweek). Permanent contract. Attractive salary package. Life and accident insurance. ️Company cafeteria (free of charge). Co-payment for voluntary health insurance. Benefits and Savings Club. Development plans, internal mobility policy. ⭐And much more! How will the Selection Process be? ️ ➡️Stay alert to your phone and email! Most likely, the first thing we will do is contact you through one of these two channels. ➡️Prepare well! We will continue with a face-to-face/virtual interview based on availability and as agreed; there may be one or two interviews, and depending on the type of process, there may also be some kind of test. ➡️Wait for the result! We care that you feel guided and know what to expect from us at every step of the selection process, so we will always try to inform you about the status of the process. Do you think this offer is not for you? Follow us on social media like LinkedIn/Instagram and stay tuned for any offers we post. Your opportunity to become a new Insuder is waiting! #InsudPharma #Challenger #Insuder #InsudTalent COMMITMENT TO EQUAL OPPORTUNITIES The InsudPharma group is aware that business management must align with the needs and demands of society, and therefore assumes the commitment to equal opportunities and treatment between men and women, as established in current regulations - Organic Law 3/2007, and we do not discriminate against anyone based on ethnicity, religion, age, sex, nationality, marital status, affective or sexual orientation, gender identity or expression, disability, or any other personal or social circumstance.

Manages quality, health, safety, and environment.