TOBLOR Consulting AB jobb

Purac designar, utvecklar och uppför anläggningar och processer inom rent vatten, biogas och avlopp. Vi är ett ledande företag inom vårt område med ca 145 anställda. Vi är etablerade i Skandinavien och Asien. Hittills har vi genomfört mer än 4000 entreprenader i 70 länder över hela världen. Läs gärna mer om oss på www.purac.se. Vill du arbeta i ett marknadsledande företag med teknik i absolut framkant, där du får chansen att arbeta multidisciplinärt med kundprojekt från anbud till färdigt projekt? Framför dig har du en enorm marknad med otaliga investeringar i VA-anläggningar där Purac kommer vara en stark spelare. Som Tekniksamordnare på Purac har du det tekniska samordningsansvaret i kundprojekt och spelar en nyckelroll i att leverera anläggningar enligt överenskommet kontrakt. Varje projekt är unikt utifrån teknisk komplexitet och sammansättning av kompetenser. Hos oss får du arbeta med intressanta och stora projekt, i en roll där du använder dina ledaregenskaper samtidigt som ditt fokus är på tekniken! Arbetsuppgifter Du kommer att driva och leda projekteringsarbete av samhällskritisk infrastruktur så som ny- och ombyggnader av anläggningar inom reningsverk, vattenverk och biogas. Du kommer arbeta i projektgrupper som medverkar i anbudskedet, för- och detaljprojektering, men också följer projektet i genomförande till överlämnad anläggning. Du ansvarar för ledning och avrapportering av det tekniska arbetet och samordnar flera discipliner så som process, mekanik, el och bygg. Du leder projekteringsmöten och ansvarar för projekteringstidplan och resursplanering av interna och externa resurser. En viktig del blir att säkerställa gränsdragningar, både internt och externt, samt upprättande av dokumentation. Rollen innebär direkt kundkontakt med beställare men också kontakter med myndigheter, konsulter och underentreprenörer. I projekten ingår du i en matrisorganisation där du rapporterar till projektledaren för respektive projekt. Du tillhör en grupp med sex kompetenta kollegor som stöttar varandra och utbyter kunskaper. Tjänsten är placerad på huvudkontoret i Lund och resor i tjänsten kan förekomma till montageplatser främst inom Sverige. Din bakgrund Vi söker en teknikintresserad projekteringsledare som trivs med att ta ledningen i projekt, samtidigt som du inte vill släppa tekniken. Vi tror att det krävs en teknisk utbildning på högskolenivå eller annan utbildning som är relevant för tjänsten. Du har några års erfarenhet från anläggningsprojektering, gärna från VA-branschen eller annan bransch med komplexa anläggningar. Vi ser helst att du har goda kunskaper i entreprenadjuridik samt förståelse för avvägningen mellan tid, kvalitet och lönsamhet. Du har god erfarenhet av projektledning och vi tror också att du är mycket teknikintresserad. Kanske är du konstruktionsansvarig eller processingenjör idag och vill ta ett nytt steg in i en roll med ett bredare och större ansvar. Goda kunskaper i både svenska och engelska är ett krav. Personlighet egenskaper Som person är du utpräglat ansvarstagande och resultatinriktad. Den kanske allra mest utmärkande egenskapen är din nyfikenhet, som innebär en vilja att lära och ett mod att ifrågasätta gällande sanningar. Du är en sann problemlösare och dina (projekt)ledande egenskaper gör att du har lätt för att samordna, kommunicera, få folk att jobba tillsammans och skapa ett bra arbetsklimat. Du har lätt för att skapa struktur och överblick, och känner dig bekväm med att fatta beslut. Purac erbjuder Inget företag erbjuder den tekniska bredd och förmåga att åta sig helhetsuppdrag som Purac. I den här rollen erbjuds du en fantastisk möjlighet att kombinera teknik i absolut framkant med att samordna och arbeta tillsammans med kompetenta kollegor – och inte minst skapa samhällsnytta! Purac besitter en enorm samlad kompetens och framför oss ligger en marknad med otaliga investeringar i VA-anläggningar. Du blir en viktig del i att bygga framtida infrastruktur som är ett måste för att klara av en ökad befolkning, klimatförändringar och nya samhällskrav. Purac präglas som arbetsplats av samarbete, transparens och prestigelöshet. Vi är stöttande, hjälpsamma och ärliga mot varandra och hos oss tillåts du påverka och omsätta dina goda idéer i praktiken. I slutändan delar vi känslan att se resultatet och säga: det här har jag varit med och skapat! Information och ansökan I det här uppdraget samarbetar Purac med TOBLOR Consulting. För mer information kring tjänsten kontakta rekryteringskonsult Tobias Lorentzon, telefon 0735-11 10 60. Tjänsten söks via TOBLORs karriärsida: www.toblor.se. Urval sker löpande varför vi gärna ser att du skickar din ansökan omgående. Välkommen med din ansökan!

Sever Pharma Solutions is an innovative contract developer and manufacturer of pharmaceuticals. It offers customers bespoke solutions through an extensive knowledge and unique manufacturing capabilities. The expertise and capabilities lie in developing and manufacturing both solid and polymer-based dosage forms. Its solid dosage portfolio includes products such as immediate-release film and non-coated tablets, along with controlled-release tablets and granules. Meanwhile it pioneers in polymer-based dosage forms with products such as vaginal rings, implants, and intrauterine systems. Currently Sever Pharma Solutions is expanding sales, staff, facilities, and its wider product portfolio. Focusing on high potent development and production, within the area of controlled release, the company has invested heavily in buildings and equipment with the aim of supporting growth and widening its core capabilities. The business is part of Sever Life Sciences which focuses on the development and commercialisation of niche hospital, and orphan products to respond to unmet medical needs and is present in 17 countries. Would you like to be part of an incredible growth journey where you will have great influence, a wide exposure internally and with considerable room for improvements? We are now looking for an Operational Excellence Manager who would like to join our team. We offer an inspiring and challenging workplace with good career opportunities. About the position As Operational Excellence Manager you will play a key role in creating and driving a company culture that strives for operational excellence through continuous improvement. You will collaborate with the management team and other stakeholders to identify high impact improvement projects that will drive efficiency and cost savings across the organization. You will be part of the Operational Excellence team in developing and delivering manufacturing excellence project/methods/activities. You will report directly to the Head of Operational Excellence. The position will include both operational and strategic responsibilities such as: - Build companywide capability by training and coaching teams in the use of LEAN methodologies, such as continuous improvement, 5S, standardization, visual management and more. - Identify and prioritize high impact improvement projects through analysis of business processes, operational metrics, and other channels. - Lead improvement projects and review performance against set targets. - Lead change and support managers during the transformation process. - Create value stream maps, process maps and documentation for existing and future processes. - Primarily workplace will be at our production site in Malmö. Qualifications We are looking for an experienced professional with a solid track record from executing projects, implementing change and with experience from manufacturing, preferably from a company being in the forefront of LEAN Production. Experience from pharmaceutical- or medical device industry will be considered a merit. The position requires a professional candidate with the willingness to learn, right attitude and a pragmatic approach. This is your preferred background: - Minimum 5 years of relevant experience. - Bachelor’s or Master’s degree in science/Engineering. - Experience from TPS, LEAN and/or Six Sigma is needed. - Demonstrated project management skills. - Demonstrated experience of driving operational cultural change. - Comfortable with learning new systems and operating within those systems. - Experience as line manager is an advantage. - Experience from GMP/GLP is considered a strong merit. - Excellence skills in Swedish and English language. - It is important for us that you share Sever Pharma Solutions’ three core values: - Making a difference - Close to the customer - Best workplace Your profile We are looking for an energetic and inspiring person with the following profile: - High commitment - can motivate and inspire others to perform at the highest standards, without being their manager. - Having the courage to question existing ways of working. - Analytical mindset. - Feel at ease, being in the centre. Why Sever Pharma Solutions? You will have the chance to be part of an incredible growth journey, with fantastic products having a positive impact on human health. This is an opportunity to work in a role with a large responsibility, but also freedom to operate and implement your ideas. You will develop relations with a majority of the company, at all levels, and the potential for improvements is considerable. Last but not least, you will work together with a much-appreciated manager! Information and application For more information about this job-opening, please contact recruitment consultant Tobias Lorentzon at TOBLOR Consulting, phone: +46 735 11 10 60. You apply for this position through TOBLOR’s career site, https://career.toblor.se/, by uploading your CV and personal letter. For more information about Sever, please visit: www.severpharmasolutions.com/. We are looking forward to seeing your application!

Camurus is a Swedish research-based pharmaceutical company committed to developing and commercializing innovative and long-acting medicines for the treatment of severe and chronic conditions, including opioid dependence, pain, cancer and endocrine disorders. New drug products are based on our proprietary FluidCrystal ® drug delivery technologies with the purpose to deliver improved quality of life, treatment outcomes and resource utilization. The company’s share is listed on Nasdaq Stockholm under the ticker “CAMX”. For more information, visit camurus.com. At Camurus you will get the opportunity to work with committed colleagues in a fantastic team, where the colleagues support and care for each other. Camurus is an innovative company that is currently expanding and establishing in new markets. Camurus is strengthening their global Patient Safety department with a new position - Patient Safety Associate. As Patient Safety Associate you will be a part of the global Patient Safety and Medical Affairs department at the headquarter in Lund, and you will report to the Director of Patient Safety. The position is based in Lund, and you will work in a dedicated team of 8 colleagues. As Patient Safety Associate you will belong to the global case processing team, with the responsibilities of monitoring mailboxes and co-ordination of case processing activities, with the aim to ensure that safety data is managed with high quality, efficiently and in compliance with worldwide pharmacovigilance regulations. Role and responsibilities Being the Patient Safety Associate, you are committed to ensure patients’ safety and product quality across the Camurus products. You will first and foremost ensure a compliant Pharmacovigilance System for Camurus products. Your responsibility includes, but is not limited to: - Management of individual case safety reports (ICSRs) and serious adverse events (SAEs) e.g. monitoring of safety mailboxes, perform ICSR download from health authorities including initial assessment, triage and logging of ICSRs and distribution of follow-up questions. - Processing of ICSRs in the Safety database - Support and perform reconciliations - Support and perform entries in XEVMPD - Support in co-ordination of activities in relation to safety in clinical trials - Support in SOP writing by preparing and reviewing Safety/PV SOPs and other related procedural documents This role involves daily cooperation with several departments internally, and it is a true coordination and spider-in-the-web type of role. Candidate profile We are looking for a candidate with a minimum of 2 years’ experience within drug/patient safety/pharmacovigilance or medical information, from the pharmaceutical/medical device industry. You probably have a background as a pharmacist, nurse or an education within pharmacology or pharmaceutical science. You have experience from managing ICSRs and SAEs, you are used to work with safety databases (e.g. ARISg/LSSMV or Argus). You have an analytical, but open mindset, you are comfortable in raising objections and enjoy solving problems and mediating issues that may arise and the ability to propose new and more efficient ways of work. To be successful in this job, you need a structural sense and attention to details. Furthermore, you enjoy working in a dynamic and changing environment. This position requires an ability to work with autonomy and independence, as well as cross-functional collaboration. You are able to prioritise effectively and meet multiple deadlines successfully. Enjoying a dynamic and multitasking business environment. A good level of spoken and written English is required. Camurus offers This is a great opportunity to join a highly innovative and dynamic company during a very exciting phase of growth. Camurus has been very successful in bringing pharmaceutical products to the market - and the ambitions are not to be lowered. With a diversified project portfolio in different stages, the commercial potential is considerable. The position offers an international work environment in a research-driven company, with the possibility make a real difference for Patient Safety. You will have the opportunity to make a career in a growing company, and you will work together with committed and knowledgeable colleagues. Camurus has approximately 200 employees with the head office located in Lund. The corporate culture is driven by innovation, strong collaboration internally and externally, ownership, quality, and passion about realizing ideas to achieve a patient-centric vision. Information and application For more information about this job-opening, please contact recruitment consultant Tobias Lorentzon at TOBLOR Consulting, phone: +46 735 11 10 60. You apply for this position through TOBLOR’s career site, https://career.toblor.se/, by uploading your CV and personal letter. For more information about Camurus, please visit: camurus.com. (https://www.camurus.com/) We are looking forward to seeing your application!

Camurus is a Swedish research-based pharmaceutical company committed to developing and commercializing innovative and long-acting medicines for the treatment of severe and chronic conditions, including opioid dependence, pain, cancer and endocrine disorders. New drug products are based on our proprietary FluidCrystal ® drug delivery technologies with the purpose to deliver improved quality of life, treatment outcomes and resource utilization. The company’s share is listed on Nasdaq Stockholm under the ticker “CAMX”. For more information, visit camurus.com. At Camurus you will get the opportunity to work with committed colleagues in a fantastic team, where the colleagues support and care for each other. Camurus is an innovative company that is currently expanding and establishing in new markets. Camurus is strengthening their global Patient Safety department with a new position -Patient Safety Manager. As Patient Safety Manager you will be a part of the global Patient Safety and Medical Affairs department and work in a dedicated team of 8 colleagues. The position is based at the headquarter in Lund and you will report to the Director of Patient Safety. You will be a part of the global case processing and surveillance, with the aim to deliver efficiency, quality, and compliance with worldwide pharmacovigilance regulations. As Patient Safety Manager you will overview cases and conduct safety surveillance by monitoring the benefit-risk balance of the products on the market and in clinical studies. Roles & Responsibilities: Being the Patient Safety Manager, you are committed to ensure patients’ safety and product quality across the Camurus products. You will first and foremost ensure a compliant Pharmacovigilance System for safety surveillance for Camurus products. You will also support the digital surveillance by using data driven methods and approaches. Your responsibility includes, but is not limited to: This role involves daily cooperation with several departments internally, and it is a true coordination and problem-solving type of role. - Have the overview of the medicinal product safety profiles and benefit-risk evaluations during its lifecycle, including monthly overview of individual case safety report (ICSR)/serious adverse event (SAE), perform signal detection and author aggregate reports. - Act as product specialist and have a good knowledge of Camurus products and ensure that information is captured and presented accurately in the safety database. - Act as subject matter expert in relation to benefit-risk evaluations. - Conduct and drive the digitalisation, automatization, and surveillance activities of safety system and database in accordance with applicable legislation. - Ensure compliance of all activities under Camurus responsibility within surveillance for Camurus products and with partners with whom Camurus hold a Safety Data Exchange Agreement (SDEA). - Conduct review and quality control of ICSRs/SAE. - Ensure timely submission and exchange of ICSRs/SAEs. - Support in the review and compilation of ICSR submission and ICSR exchange compliance. - Develop the quality system in the area of expertise, as per GVP requirement. - Support the QPPV to enable the QPPV to maintain oversight of the PV system, in particular for benefit-risk evaluations activities. Candidate profile We are looking for a candidate with a minimum of 5 years’ experience within drug/patient safety/pharmacovigilance from the pharmaceutical/medical device industry. You probably have a background as a pharmacist, nurse or have an education within pharmacology or pharmaceutical science. You have experience from ICSR/SAE processing, risk management plan writing, signal detection, aggregate report compilation, and have worked with clinical trials. Previous experience from working with case processing in safety databases is required and if you have IT experience it is a merit. Head office/Headquarters level experience is a merit. You have an analytical mindset, and you enjoy solving problems This position requires an ability to work with autonomy and independence, as well as cross-functional collaboration. You are able to prioritise effectively and meet multiple deadlines successfully. Enjoying a dynamic and multitasking business environment. A good level of spoken and written English is required. Camurus offers This is a great opportunity to join a highly innovative and dynamic company during a very exciting phase of growth. Camurus has been very successful in bringing pharmaceutical products to the market - and the ambitions are not to be lowered. With a diversified project portfolio in different stages, the commercial potential is considerable. The position offers an international work environment in a research-driven company, with the possibility make a real difference for Patient Safety. You will have the opportunity to build something from scratch, and you will work together with committed and knowledgeable colleagues. Camurus has approximately 200 employees with the head office located in Lund. The corporate culture is driven by innovation, strong collaboration internally and externally, ownership, quality, and passion about realizing ideas to achieve a patient-centric vision. Camurus offers For more information about this job-opening, please contact recruitment consultant Tobias Lorentzon at TOBLOR Consulting, phone: +46 735 11 10 60. You apply for this position through TOBLOR’s career site, https://career.toblor.se/, by uploading your CV and personal letter. For more information about Camurus, please visit: https://www.camurus.com/. We are looking forward to seeing your application!

Camurus is a Swedish research-based pharmaceutical company committed to developing and commercializing innovative and long-acting medicines for the treatment of severe and chronic conditions, including opioid dependence, pain, cancer and endocrine disorders. New drug products are based on our proprietary FluidCrystal ® drug delivery technologies with the purpose to deliver improved quality of life, treatment outcomes and resource utilization. The company’s share is listed on Nasdaq Stockholm under the ticker “CAMX”. For more information, visit camurus.com. At Camurus you will get the opportunity to work with committed colleagues in a team with good atmosphere, where the employees support and care for each other. Camurus is an innovative company that is currently expanding and establishing in new markets. We are looking for a Senior Data Manager to strengthen our Biometrics team within Clinical Development. If you have a passion for data management and enjoy collaboration with dedicated colleagues, Camurus is an excellent company for you. Main responsibility Among others, your responsibilities will include: - Support with oversight of data management activities, for example: - Data cleaning activities - EDC-system and ePRO - Perform UAT - Review/approve relevant biometrics documents - Keep up to date with data management methodology/systems relevant to the pharmaceutical industry and share knowledge - Write or review relevant SOPs - Process improvements The role is based at our HQ in Lund, Sweden. Candidate profile We are looking for a candidate with at least 5 years’ experience within Biometrics in the pharmaceutical industry, or at a clinical CRO, together with a university degree in Engineering, information technology, computer science or related field. You have experience from giving data management support and it is considered a strong merit if you have knowledge in CDISC and SAS programming. Most probably, you are an expert of EDC/ePRO system. Excellent communication skills, both oral/ and written (in English) is required, and you can easily explain complex subjects to non-experts. Even though you like working independently, you are a true team-player, with a flexible mind, able to respond to changing business needs. You are accurate, structured, and organised and you work in a goal-oriented way. Furthermore, you thrive in a dynamic environment, without being micro-managed. Camurus offers This is an excellent opportunity to join a dynamic team supporting the business in our continued growth. Camurus has been very successful in bringing pharmaceutical products to the market - and the ambitions are not to be lowered. With a diversified project portfolio in different stages, the commercial potential is considerable. The position offers an international work environment and corporate culture, with the possibility for individual development and growth. You will have great opportunities to influence, and you will work close to where decisions are taken. The team consists of three experienced, knowledgeable, and sympathetic colleagues, and you will learn a lot along the way. Camurus has approximately 200 employees with the head office located in Lund, and affiliates in 10 countries. The corporate culture is driven by innovation, strong collaboration internally and externally, ownership, quality, and passion about realizing our ideas to achieve our patient-centric vision. This is an immediate, full-time employment opportunity. Information and application For more information about this job-opening, please contact recruitment consultant Tobias Lorentzon at TOBLOR Consulting, phone: +46 735 11 10 60. You apply for this position through TOBLOR’s career site, https://career.toblor.se/, by uploading your CV and personal letter. We are looking forward to seeing your application!

KROHNE INOR är en del av koncernen KROHNE Group. KROHNE är världsledande tillverkare och leverantör av processinstrumentering och mätlösningar för många olika industribranscher över hela jorden. KROHNE INOR arbetar på en bred internationell marknad inom industrisegment som energi, kemi, olja och kärnkraft. KROHNE INOR har en ställning som en av de världsledande leverantörerna av utrustning för temperaturmätning som till stor del bygger företagets stora tekniska kunnande inom området. Utveckling av nya produkter och tekniska lösningar är en central del i företagets strategiska arbete med att bibehålla och att utveckla sin position på marknaden. För mer information, läs mer på: www.krohne-inor.se. Lockas du av att arbeta i ett teknikorienterat företag med egen utveckling och tillverkning under samma tak? Som ett led i arbetet med utvecklingen av framtida produkter söker KROHNE INOR nu, med placering i Malmö, en erfaren elektronikutvecklare med projektledaregenskaper. KROHNE INOR är en del av KROHNE Group som är världsledande inom processinstrumentering. Bolaget är i sin tur koncernens Center of Excellence i temperaturmätning. KROHNE INOR befinner sig i en spännande förändringsfas och är i behov av kreativa medarbetare. Bolaget är starkt teknikorienterat och arbetet kännetecknas av kvalitet, nytänkande och personligt engagemang. Arbetsuppgifter Rollen som projektledande elektronikutvecklare är central för att nå företagets mål att ta fram nya och innovativa lösningar. Du kommer att arbeta fokuserat med elektronikutveckling med tyngdpunkt på utveckling av inbyggda system och analog interface-teknik inom temperatursensorer. Rollen är bred med olika uppgifter inom framför allt hårdvaruutveckling och PCB-konstruktion, och du kommer att bidra både som projektledare och genom eget utvecklingsarbete. Utvecklingsorganisationen består idag av flera kompetenta medarbetare med omfattande kunskaper inom företagets teknik och produkter. Du kommer att ha ett bra stöd från en erfaren organisation och erhålla en gedigen produktkompetens. Arbetsuppgifterna består bl a av: - Ledning av elektronikutvecklingsprojekt, med hänsyn till tid, kostnad och kvalitet - Delta och bidra i utveckling av hårdvara, både nyutveckling och produktvård - Arbete med kravställning - Komponentval - PLM-hantering och projektadministration - Testning I princip är all utveckling som sker strategisk och sker både i form av system-/plattformsutveckling som utveckling av enskilda produkter. Arbetet sker enligt en koncerngemensam projektstyrningsmodell. Utvecklingsprojekt kan även ske i samarbete med KROHNE-koncernen i koncerngemensamma projekt som syftar till att utveckla gemensamma system och lösningar. Din bakgrund Vi söker dig med en ingenjörsutbildning med inriktning elektronik och minst fem års arbetslivserfarenhet från en liknande befattning. Antal år i arbetslivet är inte avgörande, men däremot ett gediget tekniskt intresse och en nyfikenhet inför komplexa problem. Du har tidigare vana av att driva produktutvecklingsprojekt mot utsatta kravspecifikationer och vi tror att du har jobbat brett med elektronikutveckling, snarare än smalt och nischat. Din erfarenhet ligger inom inbyggda system och det är klart meriterande om du har kunskaper i Visual Studio och C#/++ och/eller VB.NET. Du behärskar svenska och engelska i både tal och skrift. Personlighet För att trivas och bli framgångsrik i tjänsten tror vi att du är samarbetsinriktad och har lätt för att leda en grupp. Du är öppen och social och delar gärna med dig av dina kunskaper. I dig bor en sann utvecklare med egenskaper som kreativ, nyfiken och modig - men inte dumdristig. Det innebär att du är öppen för nya tekniska idéer och kan ta dig an komplexa problem från olika vinklar. Samtidigt som du är innovativ och idérik har du även förmågan att ta saker i mål och avsluta projekt. KROHNE INOR erbjuder I den här rollen erbjuds du goda möjligheter att utveckla dig själv och lära nya saker. Du kommer att arbeta i ett mindre och innovativt företag, med fördelen av att ingå i en större stabil koncern. Det innebär t ex goda möjligheter att påverka och göra skillnad utan att bli en i mängden, men med en internationell dimension. Det råder ett vänligt och hjälpsamt klimat i gruppen som består av fem kompetenta elektronikutvecklare. Du kommer erbjudas en gedigen introduktion och produktubildning. KROHNE INORs produkter må vara små, men är samtidigt avgörande för att optimera processer som producerar värden för miljonbelopp. De bidrar till minskat slöseri och en resurssnål tillverkning. Information och ansökan I det här uppdraget samarbetar KROHNE INOR med TOBLOR Consulting. För mer information kring tjänsten kontakta rekryteringskonsult Tobias Lorentzon, telefon 0735-11 10 60. Tjänsten söks via TOBLORs karriärsida: www.toblor.se. Urval sker löpande varför vi gärna ser att du skickar din ansökan omgående. Välkommen med din ansökan!

Saint-Gobain Ecophon develops, manufactures and markets acoustic products and systems that contribute to a good working environment by enhancing peoples’ wellbeing and performance. Our promise »A sound effect on people« is the core backbone of everything we do. Ecophon has business units in 14 countries, delegations in another 30 countries worldwide, and approximately 800 employees. The head office is located in Hyllinge, just outside Helsingborg, Sweden. Ecophon is part of the global Saint-Gobain Group. At Ecophon we believe all people deserve a good acoustic environment. We aim for creating optimal environments by developing innovative and sustainable products which create a good working environment. Coating has a crucial importance for many of the properties of our acoustic products and we see many exciting challenges and opportunities in terms of coating technology. To our R&D and Innovation organisation, we are looking for a Development Engineer within paint, woven/non-woven materials and adhesives. Responsibility Working at Ecophon is characterized by teamwork and open communication. As Development Engineer, you will work cross-functionally with colleagues throughout most of the company. This is an independent specialist role covering a large scope, and a broad spectrum of tasks. Among others, your responsibility will include: - Development of new products, solutions, ideas and concepts - Technical pre-studies and investigations - Studies of material properties - Industrialisation and factory tests at own production in Hyllinge and Næstved (DK) - Close cooperation with suppliers You will act as technical expert and support the organisation with knowledge and expertise in the field of coating. This means you will have a close collaboration with colleagues from many areas of the company, from Market/Sales, to R&D and Production; both locally and globally. You will be part of a very passionate and knowledgeable R&D team which consists of 15 Engineers, and you are reporting to Product Engineering & Development Manager. This position is based in Hyllinge, outside Helsingborg. Profile We are looking for a candidate with 5-10 years’ experience from R&D and development of products/materials. You have a good understanding of coating technologies and related areas such as paint, binders, glue and non-woven. To become successful in this role we believe you have a Master of Science degree within (physical) chemistry, preferably with specialisation in surface chemistry or polymers. Furthermore, you can communicate in English on a high level, both in writing and orally. Personality Your personality can best be described as structured and collaborative. You possess high social skills and you easily develop strong and long-term relations with both colleagues and suppliers. You are an independent self-starter, and you like to work cross-functionally. You are a “doer” that can manage several tasks and missions simultaneously without losing focus on the details. You make things happen and you are not afraid of taking initiatives and finding information on your own. Curiosity and creativity come natural to you when working with product development. Passion, Competence and Innovation are core values of Ecophon and these values influence the way of working and the products developed. Ecophon offers In this role you will have great opportunities to work in a market leading company with products enhancing peoples’ well-being and performance. You will have the advantage of working in an independent and flexible company, with the culture of a small company, but with the strength of being supported by a strong global group. Saint-Gobain invests heavily in R&D and its factories and you will have a chance to work in a creative role with strong focus on development. You will work in Hyllinge where the Ecophon headquarters is localised, where you have both R&D and production. Ecophon has historically been very successful, and the expansion and ambitions are not to be lowered - especially when it comes to sustainability. Information and application For more information about this job-opening, please contact recruitment consultant Tobias Lorentzon at TOBLOR Consulting, phone: +46 735 11 10 60. You apply for this position through TOBLOR’s career site, www.toblor.se, by uploading your CV and personal letter. We are looking forward to seeing your application!