Baxter Medical AB jobb

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. Do you want to make an impact at Baxter's thriving Luleå site in Sweden? We are dedicated to manufacturing Liko patient lifts, slings, and accessories that improve the mobility and care of individuals worldwide. Join our award-winning team, honored with the prestigious Swedish Lean Prize 2021, and contribute to a brighter future at Baxter's Luleå site as Continuous Improvement Engineer! The main purpose of the position is to lead and implement improvement modifications and support the development of continuous improvement, activities towards MIP(cost savings) and Lean Manufacturing on the site. Essential duties and responsibilities: – Other duties may be assigned: Organize, lead and participate in continuous improvement activities to meet set targets. Create project plans and drive projects for continuous improvement, as well as support managers and other teams on this field. Coordinate tasks with internal and/or external service providers. Ensure progress of strategic focus towards world class supply chain by tracking supply chain changes, risks, performance, compliance, and corporate and local plant initiatives. Overall ownership of tracking and follow-up MIP for the site in collaboration with global lead for MIP’s. Coordinate training (for example Green Belt and Lean methods) and coach the business. Lead, develop and standardize analyses and projects for the site. Back-up for the roles within the CI team. Education, experience and qualifications: Education: Bachelor’s degree in Business, Finance, Engineering or Supply Chain. Experience: 5+ years of manufacturing operations experience, 5+ years of knowledge and experience in Lean Manufacturing and Kaizen principles (Experience In a Medical Devices or Life Sciences industry is a plus. Knowledge of Lean tools, Continuous improvement, project management, MS Office. Must be fluent in Swedish and English. Effective written and oral communication skills Competencies: Ability to drive and understand continuous improvement and see the whole process with a focus on customers. Action oriented/drive for results. Ability to prioritize in a fast-paced, changing environment. Analytical approach, eager to cooperate in a team. Effective time management, problem solving and decision-making skills. Proven multi-functional team leader/member.

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. Liko AB är en del av Baxter koncernen och i Alvik utanför Luleå har vi omkring 110 anställda där vi producerar våra patientlyftar, lyftselar och tillhörande produkter. På Baxter är vi sammanbundna av vårt uppdrag. Oavsett din roll på Baxter har ditt arbete en positiv inverkan på människor runt om i världen. Du kommer att känna av vårt syfte i hela organisationen, eftersom vi vet att vårt arbete förbättrar resultaten för miljontals patienter. Baxters produkter och behandlingar finns på nästan alla sjukhus världen över, på kliniker och i hemmet. I 90 år har vi varit banbrytande för betydande medicinska innovationer som förändrar vården. På Baxter räddar vi och upprätthåller liv. På vår produktionssite i Alvik, Luleå tillverkar vi Liko personlyftar, selar och lyfttillbehör som används för att förflytta rörelsehindrade personer vid äldreboenden, sjukhus och hem över hela världen. Om tjänsten Du kommer arbeta som Kvalitetsoperatör med ansvar för kontroll och frisläppning av färdiga produkter. Alla tillverkade produkter och tillbehör går igenom kontrollen för frisläppning enligt vår process för kvalitetssäkring. Här säkerställs det att produkterna är tillverkade enligt specifikation och har godkänts i slutkontrollen. Arbetet innebär främst granskning och godkännande av produktdokumentation och det ställs höga krav på noggrannhet och förmåga att agera vid eventuella avvikelser. Du kommer även att arbeta med praktiska uppgifter så som kontroll av inkommande gods samt kontroll och sortering av avvikande material. Vi arbetar enligt LEAN-principer och vårt verksamhetssystem. Vi fokuserar på ständiga förbättringar och har en problemlösningskultur. Vi välkomnar problem, för när vi identifierar problem; kan vi bli bättre. Vi erbjuder lunch till ett förmånligt pris på vår närliggande restaurang och vi har ett personalgym samt friskvårdsbidrag. Vem du är Vi söker dig som förstår vikten av kvalitetssäkring och som har förmåga att agera vid eventuella avvikelser. Du planerar och utför ditt arbete självständigt på ett effektivt sätt med hög kvalitet. Du har ett förbättringstänk och gillar att arbeta med processer och flöden. Du är strukturerad och noggrann med en administrativ ådra. Då tjänsten innebär många olika kontaktytor och att vara en expert på ditt område så är det viktigt att du är en lagspelare och kommunikativ både i tal och skrift samt att du enkelt kan samarbeta med olika funktioner och personer. För den här rollen ser vi dig som har en gymnasieutbildning och gärna erfarenhet av liknande arbete. Du har goda kunskaper i det svenska och engelska språket och det är meriterande om du har truckkort. Anställningsform Tjänsten är en visstidsanställning med start i augusti. Det är fördelaktigt att ha körkort och egen bil för att kunna ta sig ut till Alvik då bussförbindelserna är begränsade. Tjänsten är på heltid, arbetstid är dagtid kl 7-16. Ansökan Urval och intervjuer sker löpande så tillsättning av tjänsten kan ske innan sista ansökningsdag, så sök nu!

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. As a Quality Manager you ensure product quality through the implementation of various control and improvement opportunities and coordination of work within the area of Quality Management system, CAPA and Learning Management system. Support to Sr. QA Manager in ensuring that processes needed for the quality management system are established, implemented, and maintained. Ensure the promotion of awareness of regulatory and customer requirements throughout the organization. Essential Duties and Responsibilities Management and further development of the QMS Team Intelligently deploy resources to meet daily business needs in a timely manner while evolving the work processes to become more proactive, efficient, and effective Provide strategic direction and leadership to the team to ensure operations adhere to requirements of compliance and product quality Define and coordinate tasks within the scope of the objective and task definition, as well as review and discuss work results Plan and execute local Audit program Control and track the products and processes quality and regulatory compliance through adequate performance metrics and plans. Stop, if required, the delivery and/or the production of products in case of non-conformity. Ensure that adequate records of data and results concerning tests and product controls are taken Manages effective cross-function relationships and in particular work with concept, product and commercialization teams to ensure quality of product and process. Drive data analysis of performance data to identify high priority issues relating to safety, regulatory compliance and customer satisfaction. Coordination of resources within area of Quality Management system, CAPA and Learning Management system Continuous improvements of processes within area of responsibility Implementation of the company-specific quality policy and quality goals Ensuring product conformity, reducing production deviations Ensuring compliance with design and development activities Communication of the quality principles to promote quality awareness in the company Ensuring compliance with production and process controls Ensuring product conformity, reducing production deviations Ensuring compliance with acceptance and validation activities Management of non-compliant products and investigation of problems with regards to product quality, as well as support for processing: Carry out root cause analyzes, introduce corrective measures to eliminate or reduce the identified causes. Serve as primary point of contact for quality and regulatory issues related to manufacturing processes Lead efforts to identify and execute initiatives to improve manufacturing process and product quality EDUCATION, EXPERIENCE AND QUALIFICATIONS: Proficient with Quality System Regulations, IS013485, Medical Device Regulation and ISO 13485 Quality System Standards. Demonstrated ability to succeed in team environments and possesses effective interpersonal skills. Demonstrated attention to detail, analytical decision-making, and problem-solving skills. Proven ability to succeed in an environment of continuous improvement and to identify improvement opportunities. Strong customer orientation and excellent written and verbal communication skills. Ability to effectively navigate rapidly changing quality, regulatory and business environments and succeed in an environment of change. Bachelor’s degree (minimum) in an Engineering field, preferable mechanical, electrical, or industrial engineering. 5+ years of experience in Quality Assurance or Regulatory Affairs in the Medical Device or Pharmaceutical industry. Strong management and analytical skills Strong process and continuous improvement skills Supportive, positive attitude and approach to work Good communication skills, both verbal and written Able to work independently or as part of a team Strategic skills, ability to holistic/global perspective Additional training in Risk Management, Six Sigma, Lean Manufacturing and Statistical Methods is preferred. Experience of an R&D and production site is a plus Fluent in Swedish and English, other languages are beneficial

This is where you save and sustain lives At Baxter, we are deeply connected by our mission. No matter your role at Baxter, your work makes a positive impact on people around the world. You'll feel a sense of purpose throughout the organization, as we know our work improves outcomes for millions of patients. Baxter's products and therapies are found in almost every hospital worldwide, in clinics and in the home. For over 85 years, we have pioneered significant medical innovations that transform healthcare. Together, we create a place where we are happy, successful and inspire each other. This is where you can do your best work. Join us at the intersection of saving and sustaining lives—where your purpose accelerates our mission. Baxter is seeking a Field Service Engineer to join our Technical Services Team in Sweden. The Field Engineer is responsible for the service activity on products supplied by Baxter/Hillrom in the defined geographical areas (preferred regions Göteborg or Stockholm). They will need to undertake their duties in compliance with assigned company procedures (e.g. Control of Service Documentation, Environmental Health & Safety). Key Responsibilities: Install, service, repair and maintain products, distributed by Baxter/Hillrom in the defined area of responsibility as per the defined service documentation and the quality system framework. Establish & maintain timely customer communications & relationships, along with other key stakeholders (e.g. team members and business units). Report all relevant service activity, ensuring updated and accurate service data in the service system (all work orders should be closed within the same day). Responsible for maintaining and documenting the assigned calibration equipment. Provide technical support for in-bound calls from customer & patients, document the job on the system and undertake the relevant actions. Maintain up-to-date technical competence in assigned products by successfully completing the relevant training and development. Identify opportunities for new business or business growth for products & services and escalate to the relevant stakeholders (e.g. account managers, Inside Sales). Review KPIs regularly and adapt the working practices to ensure service level is maximised. Plan and perform qualified technical training to distributors, partners, and colleagues. Co-ordinate and disseminate technical updates and bulletins. Be the technical expert and support for customers, account managers and engineers. This includes being the technical escalation point for the designated product group. Escalate and communicate updates to the monthly SME calls. Represent UKIN interests in EMEA/Global technical community. Provide technical input into contracts & tender submissions. Job Requirements: Degree, HNC/HND or equivalent level qualification in the relevant engineering field In-depth level of practical experience (minimum of 5 years of proven experience) Good IT knowledge on general connectivity, network integration of devices, wireless protocols, mobile network technologies, software support and cyber security standards would be advantageous. Frequent and regular travel within the assigned geographical region in Sweden/Nordic’s. Driving licence Fluid in Swedish and English language Your next step: If you like the sound of the above role, can thrive in a fast-paced working environment and are excited about working in a learning and growth culture, then we’d love to talk to you. Please apply directly on our Online System.