Supply Chain Specialist

Produktionsteknik och Logistik Vill du ta nästa steg i din karriär som teknisk konsult? Vill du dessutom vara med från början och bidra till hur ett konsultföretag ska utvecklas, samtidigt som du arbetar i ett intressant uppdrag hos en spännande kund? Då finns det nu en ovanlig möjlighet! Vi startar i liten skala i Sverige, men har kundavtal, resurser och tryggheten från ett internationellt konsultbolag med 40 års framgångsrik historia, gedigen teknisk kompetens och långsiktiga ambitioner. En flexibel ”startup” med erfarenhet och historik i ryggen! Vi söker ingenjörer med erfarenhet av och intresse för produktionsteknik samt förbättring av monterings- eller tillverkningsprocesser och dess logistikflöden. Kvalifikationer Formell universitetsutbildning och relevant arbetslivserfarenhet är naturligtvis viktiga, men engagemang för din egen, kundernas och företagets fortsatta utveckling är ännu viktigare. Kunskaper i svenska är meriterande och vi förväntar oss att du har giltigt uppehålls- och arbetstillstånd för att arbeta i Sverige. Om tjänsterna Flera tjänster finns tillgängliga. Det mest akuta behovet gäller: Produktionstekniker (Manufacturing Engineers) Projektledare för industrialiseringsprojekt Logistikingenjörer inom fabriksnära internlogistik, extern Supply Chain samt ILS Verktygs- och utrustningskonstruktörer (Tooling & Equipment Design Engineers), gärna med erfarenhet av Catia Lön och anställningsvillkor kommer att vara konkurrenskraftiga. Vi erbjuder Intressanta och varierande projekt hos våra internationella kunder i såväl Göteborg som andra orter Möjlighet att utvecklas till en ledande specialist inom ditt teknikområde En avslappnad och flexibel arbetsmiljö Viktigt om ditt CV Vi använder AI som komplement till våra personliga intervjuer vid matchning mot uppdrag. Se därför till att ditt CV innehåller konkreta verktyg, standarder och processer du arbetat med – ju tydligare du är, desto enklare kan vi hitta rätt uppdrag för dig. Läs mer på: https://www.comatec.fi/en/companies/comatec-sweden-ab/ Intresserad? Om du vill ta nästa steg i karriären, skicka din ansökan senast den 28:e Augusti via vårt rekryteringssystem. För mer information om denna tjänst eller andra spännande möjligheter, kontakta: Anders Rohdin E-post: anders.rohdin@comatecgroup.se Comatec Group The Comatec Group employs approx 600 skilled professionals in twenty locations in Finland, Sweden, Poland, Estonia and Romania. We provide engineering design as well as expert and project management services for the technology industry. We are at our best in projects related to mobile machinery, commercial vehicles, industrial automation and modernization, material handling, production systems, power plants and boilers. We have a vision for future growth and internationalization, and so we constantly seek new experts, especially in mechanical, electrical and automation design and in project management services. Come join us! Read more: comatec.fi

Professional Galaxy is an IT and technology consulting company that provides highly specialized expertise within IT, software development, SAP, purchasing, electronics and mechanical design. We collaborate with experienced senior experts and deliver strategic value-creating expertise to some of Sweden's most complex and analytically demanding projects. Our focus is always on high quality, professionalism and clear, measurable results. We are now seeking a Supply Chain Manager for Clinical Trial medications for one of our clients. About the assignment: Would you like to utilize your planning and supply chain knowledge to lead clinical supplies for your portfolio of global clinical studies? With constant new products and launches, there has never been a better time to join Global Clinical Supply Chain and shape our future with a significant contribution to life-changing medicines. We have an exciting opportunity for talented Supply Chain Managers to join our Clinical Study Supply Chain team in Gothenburg, Sweden. This is a key role within our Clinical Manufacturing and Supply teams, and we make sure clinical trial medications are available at the right quality, in the right quantity at the right time for every patient taking part in xx trials all over the world. Our goal is to never miss a patient. In Pharmaceutical Technology and Development (PT&D) we are the bridge which turns forward-thinking science into actual medicines that help millions of people around the world. We work across the entire value chain, crafting and delivering active ingredients, formulations and devices required to support new medicines – from supplies for use in early toxicology studies and clinical trials to developing the technology to ensure drugs can be scaled up for commercial manufacture. Tasks and responsibilities/The role: In this role you will project manage the design, plan, and set-up of the study supply chain to ensure on time delivery of clinical supplies. You will also lead a cross-functional team enabling continuous dialogue with both internal and external partners on study design requirements and associated changes which may impact the supply chain elements of the study. To be successful in this role you need to be a fast learner, self-driven and comfortable working in a high pace R&D environment. You need to be a collaborative team player, flexible and have strong communication, planning and problem-solving skills. Your main responsibilities will include: • Project manage the delivery of clinical supplies effectively and consistently, and input to the balance of costs and any risks to supply. • Ensure effective communication with project teams and key partners across a global network. • Support risk management of individual studies with proactive mitigation of risks that potentially impact the quality or delivery of supplies. • Take ownership for Inventory management including any rework and recalls, extensions of shelf life and expiry date management, or stock destruction. • Manage the Interactive Response Technology (IRT) system to execute demand and supply planning. • Work within GMP Quality Management Systems ensuring that you actively handle any deviations, complaints and change controls. Soft skills: • Strong influencing, negotiating and problem-solving skills, across geographical and cultural boundaries • Ability to adapt and operate in bespoke multiple systems. Desirable for the role: • Awareness of GMP (Good Manufacturing Practise) and GCP (Good Clinical Practice) • Knowledge of clinical development processes relevant to the supply of clinical materials • Lean knowledge and understanding • Experienced in handling Quality Events (Deviations, Change Controls, Complaints Location: Göteborg Start date: 2026-06-01 End date: 2027-05-31 Application Deadline: 2026-04-19 Are you the right person for the assignment, or do you want to recommend a strong candidate? Do not hesitate to contact us. Please apply directly through our system with: - Your updated CV in english - Availability to start the assignment In the motivation, describe why you are suitable for this assignment - refer to previous consulting assignments, employmxent, education and personal qualities. Please note: We do not accept any applications through mail. All applications have to be sent through the portal to be valid. Offer continuously: Please note that for this role we offer continuously. That means that we sometimes remove the assignments before the deadline. If you are interested, we recommend that you apply immediately.