Het overzicht van de statistiek van de lonen bij het beroep "Loss Control Manager in Belgium"

Speculative application  Skills: Acne, Actinic Keratosis, Acute Myelogenous Leukemia (AML), AIDS, Allergic Rhinitis, Allergy, Alzheimer's, Anaesthetics, Antibiotics, Anti-infectives, Anxiety, arrhythmia, Asthma, Autoimmune diseases, Autoimmune Disorder, Bacterial Vaginosis, Breast Cancer, Cardiology, Cardiovascular, chemotherapy, Chronic Lymphocytic Leukaemia, Chronic Myeloid Leukemia, Chronic Obstructive Pulmonary Disease, Clinical Pathology, CLL, Congestive Heart Failure, COPD, Cosmetics, Cystic Fibrosis, Dementia, Dentistry, Depression, Dermatology, Diabetes, Diagnostics, Dietetics, Endocrine, Endocrinology, Epilepsy, Family Medicine, Fibromyalgia, Gastroenterology, gastrointestinal, Genetic Diseases, GI, Glioblastoma Multiforme (GBM), Gynaecologic, Gynaecology, Gynecology, Haematology, Haemophilia, Heart Disease, Hematology, Hemopure Anemia, Hepatitis, Hepatology, HIV, Hodgkin's disease, Hypertension, IBD, Immunogenicity, Immunopharmacology, Infections, Infectious Diseases, Influenza, Internal Medicine, Joint Replacement, Lymphoma, Mantle Cell Lymphoma, Melanoma, Menopause, Metabolic, Migraine, Multiple Sclerosis, Musculoskeletal, Myelodysplastic Syndrome, Neonatology, Nephrology, Neurodegenerative disorders, Neurology, Neuroscience, NEUROSURGERY, non small cell lung cancer, Non-Hodgkin Lymphoma, nutraceuticals, Nutrition, OA, Obstetrics, Oncology, Ophthalmology, Oral Health, Orphan Diseases, Orphan drug, Orthobiologic Bone graft, Orthopedic Surgery, Orthopedics, Osteoarthritis, Otitis Externa, Otolaryngology, Ovarian Cancer, Paediatric, Pain, Painful Diabetic Neuropathy, Parkinson’s Disease, Physiology, Podiatry, Post-Menopausal Osteoporosis, Primary Immune Deficiency, Primary Sjogren’s Syndrome, Prostate cancer, Prostatic hyperplasia, Psychiatry, Psychology, Pulmonary, Pulmonology, RA, Rare Disease, Respiratory, retinopathy, Rheumatoid Arthritis, Rheumatology, Rhinitis, Rosacea, Schizophrenia, Seasonal Allergic Rhinitis, Severe Hemophilia, Skin Melanoma, Sleep Disorder, Sleep Medicine, Small Lymphocytic Lymphoma, Small Molecule, Smoking Cessation, Solid Tumors, surgery, Systemic Lupus Erythematosus, Systemic Sclerosis, Tissue Ablation, Transplant, Trauma, Traumatology, Type 2 Diabetes Mellitus, Urology, Vaccine, Vaccines, Vascular Diseases, Weight Loss, Women’s Health, Administrative Assistant, Agile Project Manager, Artwork Coordinator, Associate Director Clinical Operations, Associate Project Manager, Auditor, Biomedical Engineer, Biometrics Manager, Biosample Operations Manager, Biostatistician, Biostatistics Associate Director, Brand Team Lead, Business Administration Associate, Business Administration Manager, Business Analyst, Business Development Associate, Business Development Director, Business Development Manager, CEO, Change Manager, Chemical Project Manager, Chemist, Chemistry, Manufacturing & Control Lead (CMC), Chief Financial Officer, Chief Operating Officer, Chief Technical Officer, Clinical Data Associate, Clinical Data Manager, Clinical Data Specialist, Clinical Development Manager, Clinical Engineer, Clinical Lead, Clinical Operations Director, Clinical Operations Manager, Clinical Pharmacologist, Clinical Programmer, Clinical Project Manager, Clinical Research Associate, Clinical Research Director, Clinical Research Manager, Clinical Research Physician, Clinical Research Specialist, Clinical Study Coordinator, Clinical Study Manager, Clinical Supply Coordinator, Clinical Supply Manager, Clinical Trial Assistant, Clinical Trial Educator, Clinical Trial Manager, Clinical Trial Specialist, CMC Manager, Commercial Manager, Communication Manager, Compliance Associate, Compliance Manager, Computer System Validation Specialist, Contract Associate, Contracts Manager, Country Manager, Customer Service Associate, Data Analyst, Data Analytics Assistant, Data Engineer, Data Management Associate Director, Data Management, Manager, Database Programmer_Designer, Demand Planner, Demand Manager, Developer, Diagnostic Specialist, Director of Contracts & Licensing, Dispensary Assistant, Document Specialist, Drug Safety Associate, Drug Safety Director, Drug Safety Manager, Early Access Project Manager, EHS associate, Electronic Data Capture Manager, Electrophysiologist, Employer Engagement Manager, Engineer (out of industry), Epidemiologist, Exploratory Project Manager, Feasibility Manager, Freelance, FSP Clinical Manager, Global Clinical Data Manager, Graduate, Head of Clinical Data Management, Head of Clinical Operations, Head of Risk Management, Health Economist, Health Information Associate, Healthcare Compliance Manager, HR Associate, HR Manager, Imaging Operations Lead, Inhouse Clinical Research Associate, Intern, Investigator, IT Project Manager, Junior Clinical Data Manager, Junior Clinical Research Associate, Junior Pharmacovigilance officer, Junior SAS Programmer, KOL, Laboratory Assistant, Laboratory Manager, Legal Advisor, Licensing Coordinator, Logistics Associate, Logistics Manager, Logistics Supervisor, Manufacturing Manager, Manuscript Editor, Market Access Manager, Market Access Specialist, Market Insights Specialist, Market Research Associate, Marketing Associate, Material Coordinator, Medical Advisor, Medical Assistant, Medical Devices Project Manager, Medical Director, Medical Information Assistant, Medical Information Associate, Medical Information Manager, Medical Manager, Medical Monitor, medical publisher, Medical Representative, Medical Research Associate, Medical Reviewer, Medical Science Liaison, Medical Technologist, Medical Writer, Medico-economic affairs, Meeting Coordinator, MHRA Pharmacovigilance Inspector, Microbiologist, Occupational Therapist, Office Manager, Ophthalmologist, Packaging Associate, Packaging Coordinator, Patient Recruitment Coordinator, Payroll Specialist, Pharmaceutical Physician, Pharmacist, Pharmacokineticist, Pharmacology Director, Pharmacovigilance Manager, Pharmacovigilance Officer, Physiotherapist, Planning analyst, Policy Officer, Post Doctoral Researcher, Preclinical Project Manager, Principal Biostatistician, Principal Scientist, Privacy Officer, Product manager, Production Manager, Production Specialist, Program Development Manager, Programmer Analyst, Programming Associate Director, Project Assistant, Project Manager (other industry), Proposal Developer, Psychiatrist, Psychologist, Publications Manager, QPPV, Qualified Person, Quality Assurance Assistant, Quality Assurance Complaint Specialist, Quality Assurance Director, Quality Assurance Manager, Quality Assurance Specialist, Quality Control Associate, Quality Control Manager, Quality Control Specialist, Quality Engineer, Quality Manager, Quality Specialist, R&D Manager, R&D Project Manager, Record Specialist, Recruitment & Screening Co-ordinator, Registration Specialist, Regulatory Affairs Administrator, Regulatory Affairs Associate, Regulatory Affairs Director, Regulatory Affairs Manager, Regulatory Affairs VP, Regulatory Documentation Scientist, Regulatory Information Specialist, Regulatory labelling specialist, Regulatory Program Manager, Regulatory Site Activation Manager, Remote Site Monitor, Senior, Research Coordinator, Research Funding Manager, Research Team Manager, Resources Manager, Respiratory Physiotherapist, Sales Manager, Sales Rep, Sample Manager, SAS Programmer, Scientific Advisor, Scientific Affairs Associate, Scientist, Senior Associate Supply Chain (GMP), Senior Biostatistician, Senior Clinical Lead, Senior Clinical Research Associate, Senior Clinical Supply Chain Associate, Senior Clinical Team Manager, Senior Clinical Trial Manager, Senior Epidemiologist, Senior Medical Affairs Officer, Senior Nutrition Scientist, Senior Regulatory Affairs Manager, Senior Scientist, Site Engagement Manager, Site Visit Report Reviewer, SOFTWARE DEVELOPER, Software Engineer, Start Up Director, Start-up Manager, Start-Up Specialist, Strategy Lead, Study Authorisation Associate, Study Delivery Operational Specialist, Submissions Manager, Supply Chain Coordinator, Supply Chain Manager, Supply Chain Planner, Surgical Technician, Systems Administrator, Technical Project Leader, Technical Services Specialist, Training Associate, Training Manager, Translator, Validation Engineer, Vendor Manager, Veterinary Nurse, Warehouse Associate, Warehousing & Distribution Leader, BSc, CQA, GMC, MBA, MBChB, MD, MPhil, MRCPsych, MSc, No CRA Certificate, PGDip, Ph.D Statistics, Pharm D, PhD, PRINCE2, Registered Nurse, SAP, Six Sigma, SolTRAQs, Veterinary, 3PL, ADaM, Administration, Adverse Event management, Advocacy plans, Agile, AKTA, Analytical SEC, Animal Health, APICS, Applicant Tracking System Management, APS, ARISg, auditing, Batch release, Batch Review, BHV, Bioequivalence, Bioinformatics, Biologic, Biomarkers, biometrics, Biosamples, Biosimilars, Biostatistics, Biotech, Black Belt, Business Development, C++, Candidate Attraction, CAPA, CDISC, Cell Biology, Cell stem-based therapy, CER, Chemstations, Client communication, Clinical, Clinical Affairs, Clinical Data Management, Clinical Programming, Clinical Research Organisation, Clinical Trial Applications, clinical trials, close out visits, CMC, CMO, Commercialisation, Compassionate Use, Competent Authorities, Computer Systems Validation, Contract, CPIM, CRF Design, CRO, CSR, Data Analysis, data entry, Data Science, Data Warehouse, database design, Datalabs, DHPC, Distribution, Distribution Planning, DMC, Document Management, Downstream, Drug destruction, Drug Development, Drug Safety, DSUR, E2E, Early Access, Early Phase, EC Submissions, ECG, eCRF, EDC, electronic data capture, ELISA, Epidemiology, ePRO, ERP, eTMF, e-TMF, EU Legislation, Eudravigilance, European Federation of Pharmaceutical Industries, Export Management, FDA Audits, Feasibility, Finance, Forecast, FPLC, GCP, GDP, Gene Therapy, Global, Global Regulatory Affairs, GLP, GMP, Government Affairs, GS1 standards, Health Economics, Healthcare, Healthcare Compliance, Healthy Volunteers, Home-based, HPLC, IATA, ICF, ICH-GCP, Imaging, Immunology, IMP, IMPACT, IMPD, Import Management, IND, InForm, Informatics, International, Interviewing, Inventory Management, Investigator Payments, in-vitro, in-vivo, IRB Submissions, IRT, ISO 13485, ISO 13485:2003, ISO 14971, ISO 9001, ISO13485, IVRS, Java, Lab, Labelling, Laboratory, LEAN, Line Management, Logistics, MA-CC, Manufacturing, MAPP, Market Access, Market Insights, Market Intelligence, Market Research, Marketing, Marketing authorizations, Materiovigilance, MedDRA, Medical Affairs, Medical Communication, Medical Devices, Medical Information, Medical Writing, Medidata Rave, Monitoring, Monitoring Visit, MS Office, MS Project, My Trials, NMR, Office-based, Oracle, Outcomes Research, Outsourcing, Packaging, Paediatrics, Patient Outcomes, Permanent, PET scans, Pharma, Pharmaceutical, Pharmacodynamics, Pharmacoeconomics, Pharmacoepidemiology, Pharmacokinetic, Pharmacokinetics, 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SOX, SPC- CCDS, Spectroscopy, S-Plus, SPSS, SQL, Start-up activities, statistical analysis, Statistics, Study Management, Study Medication Labelling, Sunshine Act, Supplier Qualification, Supply Chain Distribution, Supply Chain Management, Supply Chain Planning, Supply Planning, SUSAR, SUSARs, TMF, Toxicogenomics, Toxicology, Trackwise, Training, Transport Management, Unicorn Purification System, UPLC, Upstream, UV-Vis Spectroscopy, validation, Veeva, Vendor Management, Venipuncture, VISIO, Western Blot, ZINC, Bratislava, Slovakia, Afrikaans, Argentinian, Armenian, Belgian, Bosnian, Bulgarian, Cambodia, Cantonese, Catalonian, Chinese, Croatian, Czech, Danish, Dutch, English, Flemish, French, Greek, Gujarati, Hebrew, Hungarian, Italian, Japanese, Korean, Latvian, Lithuanian, Luxembourgish, Macedonian, Malayalam, Mandarin, Montenegrin, Norwegian, Persian, Punjabi, Romanian, Russian, Serbian, Slovak, Slovene, Slovenian, Spanish, Swedish, Thai, Turkish, UkrainianLocation: GloballyShare: 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DESCRIPTIONOur operations network, known for our speed, accuracy, and exceptional service, delivers millions of packages and smiles to Amazon customers every day. To keep our operations network secure and assure operational continuity, we are looking for an experienced professional who wants to join our team as Senior Regional Loss Prevention Manager. In this key role, you will be accountable for the delivery of security as a service to a region, composed of multiple clusters of operational sites across the end-to-end supply chain to protect our people and prevent loss.Key job responsibilities* Be accountable to deliver strategic goals and objectives of your region* Manage a team of Cluster Loss Prevention Managers who provide security as a service to operational sites within a geographical area of responsibility that are composed of multiple clusters* Ensure all operational sites within your region are compliant with security standards, are regularly audited, and all sites have a robust physical security posture* Manage relevant risks within your region (prevention, intervention, investigation)* Engage senior management within your region to ensure a positive working relationship, understand opportunities to support, and provide security risk guidanceA day in the lifeAs a Senior Regional Loss Prevention Manager, you are responsible for a team of Cluster Loss Prevention Managers who provide security as a service to operational sites from across the Amazon supply chain within a geographical area of responsibility that are composed of multiple security clusters. You will be accountable for the performance of Security and Loss Prevention within your region. Thus, you will ensure that the region can effectively deploy resources to deliver day-to-day operational services. You prioritize incoming workload and assess risks to ensure meeting service level agreements agreed with your internal customers and proactively avoid adverse impact to the business. You will use your knowledge and expertise to coach as well as manage your entire team and to remove blockers that avoid them achieving their goals and objectives. Your team manages the day-to-day tactical and operational activities within each of the clusters; however, you will take ownership when problems become highly complex. You will ensure your team will identify, evaluate, and mitigate all security risks within your region and share findings and best practices with the wider business. You are responsible for ensuring all operational sites within your region are compliant with security standards, are regularly audited, and all sites have a robust physical security posture. You own the strategic goals within your region and manage the planning of recruiting as well as frugal deployment of resources. Finally, you will engage senior management within your region to ensure a positive working relationship, understand opportunities to support, and provide security risk guidance.About the teamSitting within the Global Security Operations organisation, Security and Loss Prevention supports the accomplishment of Amazon´s business targets and the strengthening of our brand by effectively protecting against relevant threats and by managing security and loss prevention risks that could:* Put our associates and customers under jeopardy* Disrupt the continuity of our business operations* Inflict damage to our assets* Have adverse impact on our brand reputationWorking in partnership with our stakeholders, we secure the Amazon supply chain end-to-end and promote security during business conversations. We do this by preventing security and loss prevention-related risks and vulnerabilities as early as possible, intervening in unfolding incidents to minimize any negative impact as well as thoroughly investigating security-related incidents to identify and remove root causes, preventing reoccurrence.We are open to hiring candidates to work out of one of the following locations:Berlin, BE, DEUBASIC QUALIFICATIONS* A degree or degree equivalent* Relevant advanced security- or risk-related experience (e.g., security services, asset protection, loss prevention, risk management, inventory management, investigations, supply chain, auditing, compliance, or similar) and capability to translate security concepts into actions* Relevant experience managing multiple teams dispersed across multiple regions as well as development, hiring, performance management, and managing managers* Relevant experience working with the MS Office suite (Word, Excel, Outlook) in a professional environment* Advanced proficiency in written and verbal German, upper intermediate proficiency in written and verbal EnglishPREFERRED QUALIFICATIONSPreferred qualifications are not required to apply for a position at Amazon. If you have all the basic qualifications above, we’d love to hear from you.* A relevant advanced degree, advanced degree equivalent, or industry certification* Relevant experience with physical security systems, investigation techniques, and/or management of contract security officers* Relevant experience with retail, warehouse, distribution centre services, delivery service, or supply chain* Relevant experience in business writing and communicating with a wide range of senior stakeholders* Driver’s licenseAmazon is an equal opportunities employer. We believe passionately that employing a diverse workforce is central to our success. We make recruiting decisions based on your experience and skills. We value your passion to discover, invent, simplify and build. Protecting your privacy and the security of your data is a longstanding top priority for Amazon. Please consult our Privacy Notice (https://www.amazon.jobs/en/privacy_page) to know more about how we collect, use and transfer the personal data of our candidates.m/w/d

Who are we? We care. Through pharmaceutical innovation and a strong commitment to global healthcare partnerships, we are committed to providing tools, knowledge and science to improve the health of patients worldwide. We research, develop, manufacture and commercialise our own medicines as well as a portfolio of licensed products tailored to the needs of different therapeutic areas. Today, our products are available in over 70 countries on 5 continents through 15 subsidiaries. Almirall is an international biopharmaceutical company based in Barcelona. Our strategic focus is on skin health. In order to achieve our corporate goal "Transform the patients' world by helping them realise their hopes & dreams for a healthy life.", we as a team give our best every day. Because our mission is to improve the quality of life of skin patients, understand their needs and use science to provide innovative medical solutions. The patient is always at the centre of everything we do. To fulfil our mission, we are continuously expanding our portfolio and focusing on promising innovations, particularly in the field of biologics. Our Culture At Almirall, our Noble Purpose is at the core of our work: “Transform the patients' world by helping them realize their hopes and dreams for a healthy life”. We invest in differentiated and ground-breaking medical dermatology products to bring our innovative solutions to patients in need. We listen to the patient and physician responding to their needs and helping them get the treatments they need. We are driven by science, diligent by nature.  We have a successful history in Dermatology space which places us well to create a strong footprint into specialty immuno-dermatology. Your Mission This position is based in Belgium, but covers Belgium, Luxemburg, and The Netherlands (Benelux scope). The Business Unit Director is a key member of Almirall Benelux Leadership Team, involved in the strategical cross-functional meetings, paying an active role in shaping the commercial strategy and company value. He/she is responsible for the marketing strategies and execution in Benelux, and the sales activities of the company business in Belgium and Luxemburg. The role has the full profit and loss responsibility on above scope for the sales turnover, contribution margin, trade marketing expenditure down to EBITDA. He/she will work in close collaboration with local operations and Global functions (such as Commercial GCO, Marketing, Medical, Market Access, and other needed departments) to ensure the effective execution of brand strategies. Reporting to the General Manager Benelux, the successful candidate will lead the Benelux Marketing team and the Belgian/Luxemburg Sales team. Core Responsibilities Functional leadership of Benelux marketing team, and Belgian/Luxemburg sales team. Actively participate to the leadership team, establishing key brands and portfolio value. Commercial responsibility for the entire portfolio, with a special focus on the immunology products being commercialized and ready to be launched. Ensure development of local Brands strategies with the team and cross-functional colleagues, based on Global material but local market dynamics. Set the strategic direction and drive the implementation of activities and programs to ensure best commercial value and competitive position within disease markets. Propose where and when to invest across Almirall portfolio, with key focus on biologic products; execute with tight control. Reinforce company's position in terms of Market Share and profitability. Continuous awareness of the competitive landscape and market dynamics. Translate insights into strategies and actions to overcome challenges and to leverage major local opportunities. Develop HCPs targeting, segmentation, and develop strong engagement model to optimize communication impact and value, including omnichannel. Ensure implementation of MCCP in Veeva and track performance. Put in place performance and financial measures, regularly reviewed. Identify BD or licensing partnerships opportunities for some products to create more value. The position is expected to work very closely with the various local functions, Global Commercial, Market Access and Medical Affairs and other relevant functions, playing an active role in shaping the commercial product portfolio strategy and ensuring optimal company value in Benelux. Education University degree in Life Sciences, Engineering or Business. Master´s degree is recommended. MBA is a plus. Skills Strategic thinking but also operational skills with “hands-on” approach. Ability to translate strategies into tactical execution. Management strengths, leadership skills, and influencing capabilities. Strong stakeholder management skills and customer affinity. Proven ability to develop relationship with HCPs, and relevant KOLs. Understands the needs of and challenges facing customers and looks to provide collaborative solutions that build long term relationships and partnerships. Internal stakeholder collaboration: recognition of the interdependencies among individuals and teams in achieving broader business objectives. Proactively looks to work with colleagues where shared responsibility exists and where collaboration can influence others' success. A strong team builder with excellent interpersonal skills. Honest, open-minded communicator. Able to develop and inspire commitment to a vision and lead the organization. Strong drive and proactiveness and build effective teams. Pragmatic, results oriented with strong analytical skills and business mindset. Well-structured and organized. Decisive, accountable, taking decisions, actions and responsibilities. Manages well ambiguity & complexity, including several projects with competing priorities. Capable of working in a fast-moving corporate environment. Effective presentation and communication skills (verbal and written). Fluent level of French, Flemish and English. Experience Minimum of 15 years’ experience in the healthcare industry, with a focus on commercial roles and strong sales track record. Experience in Marketing and Sales is mandatory. Experience in managing high value-added products and the launch of innovative medicines (biologics medicines). Experience in immunology is recommended, dermatology is a plus. What we offer An attractive and competitive compensation package and employee benefits. High dynamic and agile team, within a growing and transforming company. Values Care: we listen & empathize; we value diverse perspectives & backgrounds, and we help each other succeed. Courage: we challenge the status quo; we take full ownership, and we learn from our success & failures. Innovation: we put the patient and customer at the center, we create novel solutions, and we empower entrepreneurial mindsets. Simplicity: we act decisively and avoid over-analysis; we understand why before we act, and we are agile & keep things simple.

Headquartered in Norway and with more than a century of experience in renewable energy, technology and innovation, Norsk Hydro, the only fully integrated company in the aluminium sector, has 32,000 employees on 140 sites across 40 countries. Hydro combines local expertise, global reach and unrivaled R&D capabilities to serve its more than 30,000 customers. Besides producing primary aluminium, extruded products and recycling, Norsk Hydro also mines bauxite, refines alumina and generates power to become the only 360° company in the global aluminium industry. Present across the entire value chain, Norsk Hydro is committed to improving the lives of its customers and communities by shaping a sustainable future through innovative aluminum solutions.‘Hydro Extrusions’ is one of the 4 branches of activity of the Norsk Hydro group (besides ‘Hydro Bauxite Alumina’, ‘Hydro Aluminum Metal’, and ‘Hydro Energy’). ‘Hydro Extrusions’ serves customers across all industries, from automotive and mass transportation to building and construction, electronics, offshore and marine. Our experts help design and manufacture custom extrusions through to fully fabricated components.'Hydro Extrusions' is present in the Benelux with 7 factories (4 BE, 3 NL), with nearly 1,000 employees, thus offering a wide range of possibilities in extrusion, manufacturing and surface treatment solutions for our customers.On the Ghlin site, near Mons, is the largest foundry of the Extrusion Europe group (9 foundries). Equipped since 2019 with a 2nd state-of-the-art melting furnace, the Ghlin site aims to become the benchmark in green and sustainable aluminium recycling, and we are on the verge of becoming CO2 neutral in the near future. To achieve these ambitious objectives, a vast investment program in production equipment and facilities is being deployed. At the same time, a strengthening of the organizational structure is also underway. In this context we are recruiting a (m/f):You will be supporting the Casthouse Production Manager in process optimization and continuous improvement:Improve the degassing, casting, ultrasonic inspection and homogenization processes in order to reduce costs, energy consumption and melt loss.Analyze and map existing processes, analyze all parameters in order to detect anomalies, bottlenecks, yield, and quality losses. Perform internal process and product audits, and perform statistical process control of all process steps.Provide expert technical and process support for quality issues and audits.Together with the Production Manager, help spread a culture of operational excellence through 5S, Lean Manufacturing,.. and other programs.Benchmark with other Hydro casthouses throughout Europe and work on specific developments with our European R&D Center.Strong involvement in future investments in furnaces and installations for treatment, sorting and inspection in order to reach maximum casthouse safety, flexibility and sustainability. Your profile:A higher degree in engineering is a must, preferably with a metallurgy or materials science specialization. Knowledge of spectrometry is a plus.Some experience in a casthouse / foundry /… is useful, perhaps with knowledge of aluminum, but young graduates are encouraged to applyYou prefer a combination of hands-on work in an industrial environment and in-depth analysis of processesYou are passionate about your chosen field, happy to share your knowledge and with your colleagues in production, quality, maintenance and metal management and on the shop floor. Ability to work in an international and multicultural environment, fluent in French and English.Our offer:A pleasant team and an informal, results-oriented company culture.Extensive possibilities for personal development, training and international exchange within a world-wide industry leader.An attractive salary package with company car and benefits.The opportunity to contribute to a more sustainable future through innovative aluminum solutions.Hydro is heading in a new and exciting direction, and we depend on different perspectives to solve our tasks and meet customer needs. Building on our three core values –

Als Quality control & regulations Manager ben je verantwoordelijk over een team van 3 collega¿sJe zorgt ervoor om productafwijkingen tijdig te detecteren en de productieuitval zoveel mogelijk te beperken door te voorzien in referentiestalen en specificatiesJe team registreert de resultaten van de controlesJe blijft op de hoogte van elke afwijking en neemt snel de gepaste maatregelenJe zorgt met het kwaliteitslabo voor een optimaal rendement (hierbij maak je werkinstructies per test en legt deze uit)Je stuurt de laboranten correct aan en stuurt bij waar nodigJe borgt de nodige kalibraties in samenwerking met externe partnersJe staat in voor het optimaal oplossen van (interne) klachten in samenwerking met de technical support, verkoop, technische dienst, productie en labo (je analyseert de oorzaak/gevolg/kosten bij de klacht)Productwetgeving is je niet vreemdJe coördineert alle verplichtingen en acties rond reach en andere relevante wetgeving en respecteert hierbij de milieu- en veiligheidsvoorschriftenJe bent verantwoordelijk voor het opvragen en opvolgen van bepaalde externe testenJe bent verantwoordelijk voor de productcertificering en begeleidt de audits (je corrigeert de opmerkingen uit audits)Je staat in voor het formulebeheer en corrigeert elke wijziging in een formule in de betrokken velden van ons softwarepakket Navision Profil Je hebt een master diploma in de chemie of bent gelijkwaardig door ervaringJe hebt minstens 5 jaar relevante ervaring in een chemische omgeving & soortgelijke functieJe bent sterk chemie-technisch & hebt kennis van wetgeving chemieJe kan je team enthousiasmeren en bent een echte peoplemanagerJe kan goed zelfstandig functioneren en bent assertiefJe kijkt vooruit en kan snel anticiperen indien nodigJe spreekt vlot Nederlandse, Frans en Engels (geschreven/ gesproken)Je werkt nauwkeurigJe denkt en handelt innovatief, kan goed omgaan met verandering Connaissances linguistiques Frans : Goed Nederlands : Goed Engels : Goed

Integrated DNA Technologies (IDT) is an American company, part of the Danaher group. Our European activities are based in Leuven, Belgium. IDT¿s core business is the production of short DNA strands called oligonucleotides, which can be used for various purposes like diagnostic tests for breast cancer, AIDS or COVID-19, research to discover new drugs and producing safer and more plentiful agricultural products. Although being a young company, IDT managed to become market leader in oligonucleotide synthesis worldwide thanks to the fantastic team work of all its associates and the constant innovation of its products. We are currently looking for a new junior manager to guide IDT¿s GMP (Good Manufacturing Practices) team in Leuven. At this production unit oligonucleotides are being manufactured in order for customers to use them for molecular diagnostics. As the Junior Manager of GMP Manufacturing you get the chance to develop, coach and mentor a young, driven and specialized lab team. Your aim is to build the team further and make sure to create an environment where every team member feels valued and recognized and where open communication is key. You bring the team to the next level by increasing its efficiency and by building a story where all members fit in perfectly. The ideal candidate has a background in science, a first experience with people management and knows what it¿s like to work in a manufacturing environment. A high proficiency in English is required. Knowledge of Dutch is definitely a bonus. ResponsibilitiesSupervise the daily activities of the GMP team and set priorities for the team to ensure task completion and coordinate activities with other supervisors. Supervision of the GMP Manufacturing staff would include employee hiring, training, evaluations and discipline.Maintain an environment for employees in which they feel like their opinions are valued, their actions make a difference, they understand management¿s expectations of their performance, and they have the resources needed to perform their job effectively.Ensure the efficient production of oligonucleotide synthesis, purification, and formulation and use judgment to identify, troubleshoot and resolve day-to-day technical and operational problems.Facilitate communication between production personnel and management.Use judgement to identify the need for documentation/process changes, process deviations, product non-conformances, and other occurrences that can indicate the ineffectiveness of quality and/or manufacturing systems.Assist in prioritizing the workflow of production through the lab.Develop and monitor performance goals and metrics and impact the quality, efficiency and effectiveness of own team.Coordinate the development of standard procedures used for customer specific products as well as customer specific documentation necessary to meet the customer¿s requested specifications.Identify features and characteristics of processes and products that bear on the ability of the finished product to satisfy fitness-for-use; including safety and performance.Maintain a constant awareness for product defects, which may occur from the improper performance of specific tasks.Contribute to the implementation and improvement of quality (QMS) and environmental management systems (EMS) by: being aware of and reporting changes that may affect QMS and EMS related aspects, actions and objectives of the relevant department, assist in related actions and management programs as required. Profil At least a Bachelor¿s degree in a science related field (chemistry preferred).Min. 3 years of successful experience in manufacturing. Experience with oligonucleotide manufacturing is a big plus.Excellent leadership skills.Ability to effectively communicate with all levels of personnel as well as customers.Ability to encourage and facilitate cooperation, teamwork and pride.Excellent computer skills and the ability to quickly learn new software.Extensive knowledge of GMP/ISO 13485 standard.Ability to multitask with excellent attention to detail.Adaptability to perform under stress.Adaptability to perform a variety of duties, often changing from one task to another without loss of efficiency or composure.Ability to maintain both a high standard of courtesy and cooperation in dealing with co-workers.Ability to accept responsibility for the direction, control or planning of an activity.Adaptability to situations requiring the precise attainment of set limits, tolerances or standards.Adaptability to perform repetitive work or to perform continuously the same work, according to set procedures sequence or pace. Connaissances linguistiques Engels : Goed