Lediga jobb TOBLOR Consulting AB i Lund

Camurusis 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 proprietaryFluidCrystal 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.

AtCamurusyou will get the opportunity to work with committed and knowledgeable colleagues in a fantastic Regulatory Affairs teamwith a friendly, supportive atmosphere.Since one of our colleagues are taking on new challenges internally, we are now looking for its successor.

In this position you will be part of the CMC Regulatory Affairs team, in the global Regulatory Affairs organisation, at the headquarters in Lund. The team today consists of four colleagues working with CMC regulatory affairs activities, covering all Camurus’ products and projects. You will work in an international environment requiring a high level of flexibility.
This is a key position to support drug development, clinical trials and commercialization of new products, as well as maintaining products already on the market. You will get the chance to work with different markets like US, EU and rest of the world.
Your responsibility:
Lead and implement CMC submission strategies/activities for development projects and registered products, including maintenance and life-cycle management plans.
Compilation, review and update of CMC-related documents in clinical trial and marketing authorization applications.
Prepare for Health Authority meetings for CMC regulatory matters.
Respond to CMC questions from Health Authorities.
Manage maintenance activities for registered products, including regulatory impact assessment of CMC changes and compilation of post-approval submissions.
Provide CMC regulatory expertise in cross-functional project teams.
Represent and drive CMC-related activities in cross-functional collaboration.
Develop and improve processes and ways of working.


Candidate profile We are looking for a candidate with at least 5 years of professional Regulatory Affairs experience, working on pharmaceutical regulatory affairs activities, including maintenance and life-cycle management activities for US and EU. You have profound knowledge within the CMC regulatory area and proficiency in relevant regulatory-related regulations and guidelines. It is an advantage if you are familiar with drug-device combination product regulations. Most probably,
you have a good understanding of drug development processes. You have a Bachelor or Master of Science degree.
Excellent communication and documentation skills (oral/written) in English are required, together with project management skills.
To be successful in this role, you need a structured and organised mindset together with strong focus on details and time management. Even though you are highly structured, you support change and can adapt to new conditions. We value a supportive and flexible “roll up the sleeves” attitude. You see solutions rather than problems and you possess a strong personal drive.

Camurus offersThis is a great time to join a highly dynamic company during an exciting phase of growth. Camurus has been very successful in bringing pharmaceutical products to the market - and the ambitions are to continue in the same way. With a diversified project portfolio in different stages, the commercial potential is considerable. This position offers a fantastic opportunity to join a competent and committed CMC Regulatory Affairs team – where we care for each other, and where the laughter is never far away. We offer you an interesting journey being part of supporting new market applications (NDA, MAA), but also maintaining existing products on different markets.
Camurushas approximately 230 employees with the headquarters located in Lund. The corporate culture is driven by innovation, strong collaboration internally and externally, ownership,quality, and passion about realizingideasto achieve a patient-centric vision.

Information and applicationFor 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: www.camurus.com/.
We are looking forward to seeing your application! Visa mindre

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! Visa mindre

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! Visa mindre

Bertin Exensor är en världsledande leverantör av taktiska marksensorer (Unattended Ground Sensors -UGS) och vi tillhandahåller kompletta lösningar för klassificering och identifiering av potentiella hot på marken. Våra system innehåller den senaste sensortekniken samt kameror med rörelsedetektering. Kompletta lösningar kan även innehålla mastburna kameror, radarsystem och specialkameror med lång räckvidd. Exensor är ett dynamiskt företag med internationell arbetsmiljö och företagskultur i en spännande fas av tillväxt, med stor möjlighet till individuell utveckling.

Tilltalas du av att jobba i ett marknadsledande företag med produkter i absolut teknisk framkant? Till ett bolag i otrolig tillväxt ges här en fantastisk möjlighet att tillsammans med kompetenta kollegor arbeta i en bred roll med stort inflytande, och samtidigt ha roligt på vägen!



För dig med passion för teknikutveckling och intresse för maskininlärning och algoritmer kommer här en speciell möjlighet: Bertin Exensor, en världsledande leverantör inom skräddarsydda sensorlösningar till försvars- och säkerhetssektorn söker nu en algoritmutvecklare.

Om rollen

Vi söker en driven utvecklare som kan bidra till vårt växande utbud av sensorer. Dina arbetsuppgifter inkluderar design, implementation, simulering samt även praktiska fälttester av sensorlösningar.

Ansvarsområden och dagliga arbetsuppgifter:

- Kravställningsarbete

- Design av algoritmer och lösningar i enlighet med kravställning

- Algoritmutveckling i Matlab/Simulink

- Test och validering av algoritmer, både via simulatorer och fälttester

- Delta i arbetet kring företagets långsiktiga planering för algoritmer och maskininlärning/AI

- Arbeta med externa forskningsprojekt

Som algoritmsutvecklare kommer du att vara en del av Bertin Exensors algoritmgrupp som har gemensamt ansvar för företagets alla algoritmbaserade förmågor.



Din bakgrund
För att ta dig an rollen krävs en civilingenjörsutbildning, eller motsvarande Masterexamen, inom matematik, fysik, datateknik eller liknande. Du behöver dessutom erfarenhet inom ett eller flera av följande områden; signalbehandling, bildanalys eller maskininlärning. Du har god kunskap om matematiska modeller och signalanalys.

Vi ser gärna att du har dokumenterad arbetslivserfarenhet av något eller flera av följande områden: Matlab/Simulink, C/C++-programmering för inbyggda system, modellbaserad utveckling, algoritmdesign på enheter med begränsade resurser samt analys av sensordata. Det är även en fördel med erfarenhet från militärtjänstgöring. I rollen behöver du behärska svenska och engelska flytande. Svenskt medborgarskap är en förutsättning.

Vår sensorplattform innehåller ett brett spann av sensortyper så erfarenhet av följande områden är meriterande; optiska och termiska sensorer, seismiska, akustiska och magnetiska sensorer samt radar och lidar.

Personlighet
På Bertin Exensor väntar vi inte på att möjligheterna ska hända, vi skapar dem. Därför är viktiga egenskaper för att passa in hos oss att aldrig att ge upp, att agera aktivt och ha en stark vilja att ta initiativ. I rollen involveras du i flera projekt samtidigt, så det är viktigt med smidighet, fokus och kommunikationsförmåga. Förutom att ha ett starkt intresse för teknik så tror vi också att du självständigt får saker gjorda och har ett arbetssätt som är lyhört, strukturerat och organiserat. I samarbete med kollegor, lokalt och på distans, behövs en påhittig lagspelare och en pålitlig person med ett professionellt förhållningssätt.



Bertin Exensor erbjuder
Bertin Exensor erbjuder dig en intressant möjlighet att jobba med den senaste tekniken inom avancerade sensorsystem. Ingen annan aktör erbjuder motsvarande system och helhetslösning. Du kommer att jobba med kompetenta och passionerade kollegor i en miljö som präglas av samarbete, engagemang, teknikintresse och humor. Gemenskapen är stark och tillåter oss ha roligt längs vägen. Bertin Exensor befinner sig i en positiv trend och uppvisar goda lönsamhetssiffror och med en stark internationell ägare spås en lysande framtid. Ett trevligt kontor och gemensamma aktiviteter för personalen är självklarheter.



Information och ansökan
I det här uppdraget samarbetar Bertin Exensor 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! Visa mindre

BONESUPPORT (Nasdaq Stockholm: BONEX) develops and commercializes innovative injectable bio-ceramic bone graft substitutes that remodel to the patient’s own bone and have the capability of eluting drugs. BONESUPPORT’s bone graft substitutes are based on the patented technology platform CERAMENT. The company is conducting several clinical studies to further demonstrate the clinical and health economic benefits its products deliver. The company is based in Lund, Sweden, and the net sales amounted to SEK 329 million in 2022. Please visit www.bonesupport.com for more information.

BONESUPPORT and CERAMENT are registered trademarks of BONESUPPORT AB.

Come and join a global emerging leader in orthobiologics with a vision to optimize bone biology for the treatment of bone disorders! Here is a chance to contribute with your experience in an value-driven and creative company with extraordinary products. Together with bright colleagues at BONESUPPORT, you will make a difference in restoring health to improve the quality of life for patients with bone disorders.

BONESUPPORT is an innovative and rapidly growing orthobiologics company, based in Lund, Sweden. To further strengthen the R&D organization and future product portfolio, BONESUPPORT is now looking for an a experienced and innovative Biology & IP Specialist.

The role

As the Biology & IP Specialist you will spend a majority of your time in leading and supporting early research of new product development in the field of synthetic bone graft substitute (class III implant device/drug combination products). You will also lead and manage our patent portfolio, identify, and discuss ideas and assess their patentability. You will take part in improvements and development as a subject matter expert and provide deep scientific knowledge in understanding the biology of bone remodelling, osteoinduction and orthobiologics. Depending on which strengths you bring, you will also be part of shaping the role going forward.

Biology part:

- Be responsible for and drive research activities which concern the biology part of our products.

- Strengthen early product research and development together with existing team.

- Plan, perform and report investigation and verification studies.

- Act as Project Manager in selected projects.

IP part:

- Lead and manage BONESUPPORT patent portfolio.

- Defend the portfolio and participate in opposition and appeal proceedings.

- Invention harvesting, identify and discuss ideas and assess their patentability.

- Explore freedom to operate (FTO) and write patent applications.

- Collaborate with patent attorneys to oversee the competitor patent landscape.

Your profile

For this position, we are looking for a person with the following experience and qualifications:

- M.Sc. or higher in Biology, Formulation Chemistry or related science field.

- Experience from early stage of R&D and product development.

- Experience from working with intellectual property, patent applications and freedom to operate.

- Experience in orthobiologics.

- Innovative mindset with good presentation and communication skills.

We consider it a merit if you have:

- Experience from medical device or pharma industry.

- Experience in project management.

- Knowledge about bone graft substitutes.

- Understanding of ISO 13485 and documentation requirements according to design control processes and in Medical Device Regulation.

- A broad international network in relevant areas.

At BONESUPPORT we value personal skills as much as professional qualifications, and in this role we are looking for a reliable, innovative and self-motivated person with excellent communication skills verbally and written. You need to be flexible and able to adjust to current conditions and have strong collaboration and organizational skills.

Why BONESUPPORT?

At BONESUPPORT you will be working together with skilled, dedicated people who enjoy working in a fast growing and innovative organization. We offer a dynamic and stimulating workplace and strive for generating great teamwork, innovation, passion, and performance - which is reflected in impressive employee engagement figures. We believe in our journey and take pride in what we do!



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! Visa mindre

BONESUPPORT (Nasdaq Stockholm: BONEX) develops and commercializes innovative injectable bio-ceramic bone graft substitutes that remodel to the patient’s own bone and have the capability of eluting drugs. BONESUPPORT’s bone graft substitutes are based on the patented technology platform CERAMENT. The company is conducting several clinical studies to further demonstrate the clinical and health economic benefits its products deliver. The company is based in Lund, Sweden, and the net sales amounted to SEK 329 million in 2022. Please visit www.bonesupport.com for more information.

BONESUPPORT and CERAMENT are registered trademarks of BONESUPPORT AB.

Come and join BONESUPPORT as Project Manager! Here is a chance to contribute with your experience in an agile and creative company with extraordinary products!

BONESUPPORT is an innovative and rapidly growing orthobiologics company, based in Lund, Sweden. To further strengthen the company, BONESUPPORT is now looking for an experienced and driven Project Manager to be a part of our Program Office.

Your mission

You will have the responsibility to lead and manage projects primarily within Operations, manufacturing process improvements and support to existing products to ensure on time and within budget delivery through effective management of BONESUPPORT resources. This role encompasses both hands-on project management activities as well as overall inter-project coordination. You will be located in our headquarter in Lund, Sweden.

Purpose and summary of position:

- Establish, lead and transfer of manufacturing improvement projects within Operations

- Lead the development of overall project scope and execution strategy

- Lead the development of cost estimate for funding requests

- Based on project requirements, propose suitable team’s to execute the project’s

- Execute project tasks as required.

- Control of cost, schedule and scope within corporate guidelines

Your profile

We believe that you are an experienced and driven project manager with minimum 3-5 years in project management, within medical device/pharma projects preferably within manufacturing and operations. You have a technical academic background preferably from validation or production engineering on a Bachelor/Master level or similar.

Experience from R&D working with manufacturing and design transfer activities and/or product lifecycle management (a “hands-on” person) is an advantage. Furthermore, previous experience working with CMO´s would be of advantage. Having medical device development experience is preferred along with a solid working knowledge of MDR, FDA Quality System Regulations and ISO 13485.

We think that you have demonstrated success leading, facilitating and motivating cross-functional peers and teams, and you are capable in managing multiple projects simultaneously. For this position you need to be able to communicate in English on a high level.

At BONESUPPORT we value personal skills as much as professional qualifications, and in this role, we are looking for a dedicated and self-driven person with great collaboration skills who also have a genuine interest in medical device and Product Lifecycle Management. You need to be fluent in English and it is an advantage if you also read and speak Swedish/Scandinavian.

Why BONESUPPORT?

At BONESUPPORT you will be working together with skilled, dedicated people who enjoy working in a fast growing and innovative organization. We offer a dynamic and stimulating workplace and strive for generating great teamwork, innovation, passion, and performance - which is reflected in impressive employee engagement figures. We believe in our journey and take pride in what we do!

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! Visa mindre

BONESUPPORT (Nasdaq Stockholm: BONEX) develops and commercializes innovative injectable bio-ceramic bone graft substitutes that remodel to the patient’s own bone and have the capability of eluting drugs. BONESUPPORT’s bone graft substitutes are based on the patented technology platform CERAMENT. The company is conducting several clinical studies to further demonstrate the clinical and health economic benefits its products deliver. The company is based in Lund, Sweden, and the net sales amounted to SEK 329 million in 2022. Please visit www.bonesupport.com for more information.

BONESUPPORT and CERAMENT are registered trademarks of BONESUPPORT AB.

Come and join BONESUPPORT as Design Control Engineer! Here is a chance to contribute with your experience in an agile and creative company with extraordinary products!

BONESUPPORT is an innovative and rapidly growing orthobiologics company, based in Lund, Sweden. To further strengthen the company, BONESUPPORT is now looking for an experienced and driven Design Control Engineer with specialty in Labeling and Risk Management to be a part of our company.

The role

You will work with Product Lifecycle management of BONESUPPORT’s products, with a focus on labeling and risk management. You will be responsible for that the products are in compliance with the regulatory requirements including also compliance with up-dated standards, guidelines and regulations throughout the lifecycle of the products by up-dating, reviewing and establishing engineering documents and Standard Operation Procedures according to the regulatory requirements with a labeling and risk management focus. In this position, you will also have the main responsibility for the Risk Management process according to ISO 14971.

In your role as Design Control Engineer in the Development & Engineering department, you will collaborate closely with Quality, Regulatory, Research and Operations as well as with external partners.



Your profile

For this position, we are looking for a person with the following experience and qualifications:

- Technical academic background on a bachelor level or higher

- At least four years’ relevant experience from the medical device industry

- “Hands on” experience of leading activities connected to labeling, Risk Management ISO 14971 and technical documentation (design control documentation)

- Medical Device Regulation (MDR 2017/745) experience preferred along with a solid working knowledge of FDA Quality System Regulations and ISO 13485

- Experience in leading the creation of design and development documentation to support the regulatory files and to support clinical studies according to FDA, ISO and MDR

It will be seen as a merit if you have knowledge and experience in class III implant products and sterilization processes.

At BONESUPPORT we value personal skills as much as professional qualifications, and in this role, we are looking for a dedicated and self-driven person with great collaboration skills who also have a genuine interest in medical device and Product Lifecycle Management. You need to be fluent in English and it is an advantage if you also read and speak Swedish/Scandinavian.



Why BONESUPPORT?

At BONESUPPORT you will be working together with skilled, dedicated people who enjoy working in a fast growing and innovative organization. We offer a dynamic and stimulating workplace and strive for generating great teamwork, innovation, passion, and performance - which is reflected in impressive employee engagement figures. We believe in our journey and take pride in what we do!



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! Visa mindre

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 Green Tech-bolag med teknik i absolut framkant, där du får chansen att i nära samarbete med kompetenta kollegor vara med från idé till färdig anläggning?

Vi på PURAC befinner oss i en expansiv fas och har därför ett behov av att utöka med flera rör- och anläggningskonstruktörer. Då vi på flera platser i Norden vunnit stora kontrakt som sträcker sig över de kommande åren söker vi nya kollegor på samtliga våra kontor (Lund, Kungsbacka, Kristianstad, Stockholm och Kalmar). Puracs huvudkontor finns i Lund och i denna rekrytering söker vi konstruktörer och konstruktionsansvariga till vårt konstruktionsteam med placering i Lund eller Kristianstad.



Arbetsuppgifter

Som rör- och anläggningskonstruktör hos oss får du möjlighet att arbeta med konstruktion av anläggningar inom vattenrening och biogas. Huvuddelen av arbetet kommer att utföras i utförandefasen av projekten där du arbetar med flödesscheman, layouter, tillverkningsritningar, rörkonstruktion, hydrauliska beräkningar, hållfasthetsberäkningar, underlag för CE-märkning, material- och komponentspecifikationer med mera. Vår projektering utförs huvudsakligen i AutoCad, Plant 3D och i Inventor. Som konstruktör kommer du även att bli inblandad i förstudier/utredningar, förprojekt, upphandlingar, ta fram förfrågningsunderlag för rörinstallationer mm.

Vi på PURAC tar inte bara fram handlingar utan vi driver och genomför även projekten ute hos kund med hjälp av vår egen personal och vid behov underentreprenörer. Ibland så är det vi som har helheten mot slutkund och ibland går vi in som en underleverantör. Så hos oss får du som konstruktör ofta vara med från början till slut i dina projekt vilket ger en bra omväxling i ditt dagliga arbete och en bra feedback på de lösningar som du designat.

Vår breda bas innebär att du som konstruktör får tillgång till en bred intern kompetens som du kan utnyttja och ta hjälp av när du genomför dina uppdrag. Designdelen av våra projekt genomförs normalt på våra egna kontor och ofta i projektteam med kompetens sammansatt från de olika kontoren.



Din profil

När det gäller din bakgrund så tror vi att det finns flera möjliga vägar till att bli en duktig konstruktör. Det som är avgörande för oss är dina personliga egenskaper och drivkrafter.

Tidigare erfarenhet från vattenrening och biogas, alternativt anläggningsdesign inom annan processindustri, är meriterande liksom kunskap inom AutoCad, Plant 3D och Inventor.

Vi ser gärna att du:

- har en relevant utbildning eller motsvarande erfarenhet

- redan idag är verksam i branschen som konsult, konstruktör, montage- eller projektledare

- drivs av att hitta lösningar på kundens problem

- vill utveckla och utvecklas i ett expansivt företag

- är kommunikativ såväl som god lyssnare och lagspelare

- behärskar teknisk svenska och engelska bra, i såväl tal som skrift

Purac erbjuder

Vi på Purac är experter på att designa, utveckla och uppföra anläggningar och processer inom rent vatten, biogas och avlopp. Vi är ett ledande företag inom vårt område och inget företag erbjuder den tekniska bredd och förmåga att åta sig helhetsuppdrag som Purac. Vi finns etablerade i Skandinavien och Asien och har hittills genomfört mer än 5000 entreprenader i 70 länder över hela världen.

Hos oss får du arbeta med kunniga kollegor, intressanta projekt och med stor möjlighet till utveckling. Du blir en viktig del i att bygga framtida infrastruktur som är ett måste för att klara av en ökad befolkning, klimatförändring och nya samhällskrav - ett arbete som är av stort värde för både människa och miljö. Purac präglas som arbetsplats av samarbete, transparens och prestigelöshet. Vi är stöttande, hjälpsamma och ärliga mot varandra och hos oss får du 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! Visa mindre

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 highly knowledgeable colleagues in a fantastic team, where the colleagues support and care for?each other.?Camurus?is?an innovative and research-driven company where your contribution can make life easier for many patients.

In this position you will report to Medical Director Neuroscience and be part of the Medical Affairs team. You will work very close with your Neuroscience Brand Team and your responsibility will be the Nordic countries, with a special focus on Sweden and Denmark.

As Medical Advisor, you will provide medical and scientific support, externally to customers and internally to other functions in the organization within all Nordic and Baltic countries. You will meet for example doctors, nurses, and other functions in opioid dependence treatment teams.

Your responsibility includes, but is not limited to:

- Timely and high-quality deliverables from Medical Affairs including medical and scientific support.

- Responsible for Medical Affairs strategy, including budget of the region.

- Representing the medical function in relevant internal and external cross-functional meetings in the Nordics and Baltics.

- Management of key external experts in the region.

- Ensure internal and external medical expertise is provided to the company to set-up and govern medical education, scientific exchange, and scientific communication activities in the region, in collaboration with Global Medical Affairs and other relevant functions.

- Act as a medical contact for company sponsored clinical trials and real-world evidence activities in the Nordics and Baltics.

- Assist the global Medical Affairs organization as needed at international meetings and conferences.

This role involves frequent traveling within the Nordic countries, mainly Sweden and Denmark. Preferably, you will be based close to an international airport, and you are able to work on a fully remote basis.



Candidate profile
We are looking for a candidate with a minimum of 3 years’ experience from Medical Affairs. You have a Master of Science degree, or equivalent medical related degree, preferably combined with a PhD.

You have experience from working with field-based customer facing activities and you are able to travel up to 50% of your time. Driving license will be required.

You possess excellent communication and interpersonal skills, which means you can develop strong relationships with key opinion leaders and external stakeholders. You have demonstrated skills in delivering high quality and trustworthy scientific presentations and you are familiar with relevant product related compliance requirements in the region. This position requires an ability to work with autonomy and independence, as well as cross-functional collaboration.

A good level of spoken and written English is required. Fluency in Swedish or Danish is considered a strong merit.



Camurus offers
This is a great time 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 the patients. You will have great opportunities to influence, and you will work together with extremely 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! Visa mindre

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 (http://www.purac.se/).

Vill du arbeta i ett marknadsledande företag med teknik i absolut framkant, där du får chansen att spela en avgörande roll för att säkra leveranser till kunder och påverka företagets lönsamhet?

Som process- och utvecklingschef på Purac har du det långsiktiga ansvaret att utveckla en avdelning med ca tio processingenjörer. Det är en nyckelroll för att skapa en konkurrenskraftig leverans till kunder, som bygger på effektiv projektmetodik, processteknik i framkant och spetskompetens hos medarbetarna.



Arbetsuppgifter

Du kommer ha komplett personal-, budget- och resultatansvar för din avdelning och stort fokus kommer ligga på att utveckla medarbetare, driva kompetensutveckling och att skapa en arbetsmiljö med hög trivsel och bästa förutsättningar att kunna leverera lönsamma kundprojekt. Du har ett strategiskt ansvar för att driva och följa upp avdelningens projektresultat samt att arbeta kontinuerligt med förbättringsarbete. Ytterligare ett fokusområde kommer vara att utveckla processer, metodik och arbetssätt för att säkerställa effektiva och lönsamma kundprojekt. Tjänsten innebär en central position inom Purac med mycket samverkan både internt och externt. Internt bistår avdelningen med processtekniskt säljstöd till försäljnings- och marknadsavdelningarna. Du kommer också bevaka teknikutvecklingen inom de områden som Purac är verksamma inom och tillsammans med marknadsavdelningen styra framtida satsningar inom teknikutveckling. Du representerar även Purac på strategiskt viktiga konferenser och seminarier. Du rapporterar till teknisk chef och tjänsten kommer med fördel vara baserad i Lund, men möjlighet finns att utgå från Göteborg eller Stockholm. Resor i tjänsten kan förekomma såväl inom Sverige som utomlands.



Din bakgrund

Vi söker dig med minst tio års erfarenhet av praktisk processdimensionering av kommunala och industriella avloppsreningsverk, dricksvattenverk eller biogasanläggningar. Du har en teknisk högskoleutbildning på motsvarande civilingenjörsnivå och en mycket god teknisk förståelse relaterad till VA-branschen och dess applikationer/processer. Mest sannolikt är att du idag har personalansvar eller att du som projektledare har erhållit en gedigen erfarenhet av ledarskap.

Du är en utpräglat affärsmässig ledare som drivs av att med hjälp av din grupp leverera lönsamma projekt. Goda kunskaper i både svenska och engelska är ett krav.

Personlighet och ledarskap

Som person är du utpräglat ansvarstagande och resultatinriktad, men med en ödmjuk och prestigelös attityd. Du förespråkar samarbete och har lätt för att kommunicera, både i tal och skrift. Förändringar ser du som något positivt och du är naturligt nyfiken och tar snabbt till dig teknisk utveckling. Som ledare driver du mot resultat och agerar affärsmässigt med ett stort mått av proaktivitet. Du uppfattas som en naturlig förebild som involverar och inspirerar och som ständigt strävar efter att utveckla både dig själv och dina medarbetare.

Purac erbjuder

Detta är kanske det häftigaste jobb du kan ha om du har en processteknisk bakgrund och är verksam inom VA-branschen i Sverige! 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 utveckla en synnerligen kompetent grupp. Framför dig ligger spännande utmaningar men också stora möjligheter att påverka internt och åstadkomma resultat.

Purac präglas som arbetsplats av samarbete, transparens och prestigelöshet. Vi är stöttande, hjälpsamma och ärliga mot varandra och hos oss får du 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! Visa mindre

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 Statistician/Programmer with great CDISC-knowledge and ability to drive statistical activities. If you have a passion for statistical analysis and enjoy collaboration with dedicated colleagues, Camurus is an excellent company for you.



Main responsibility
Among others, your responsibilities will include:

- Provide input to relevant section in the Clinical Trial Protocol and approve/sign off.

- Lead or write SAP for a trial and for other non-study analysis of data and sign off.

- Review and approve/sign off Clinical Trial Reports

- Provide statistical input to clinical programs, study designs and sample size calculation

- Program statistical analyses on clinical data

- Oversight and QC of CRO deliverables regarding biometrics activities

- Support with statistical/programming input to regulatory interactions

- Develop internal statistical/programming processes

- Provide CDISC input to programming activities

The role is based at HQ in Lund, Sweden.

Candidate profile
We are looking for a candidate with at least 5 years’ experience within Statistics and CDISC-programming in the pharmaceutical industry, or at a clinical CRO, together with a university degree in Statistics. You have experience from programming in SAS, in connection to clinical study data analysis, and you have an interest in developing your programming skills and to become an expert in statistical models and analysis. Excellent communication skills, both oral/ and written (in English) is required.

You have a strongly analytical personality, and you feel comfortable questioning facts and figures. You are accurate, structured and organised, but at the same time open and proactive.

Camurus offers
This is a great time to join a highly 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 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. Camurus?has approximately 190 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 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. For more information about Camurus, please visit: https://www.camurus.com/.

We are looking forward to seeing your application! Visa mindre

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 in new markets. We are looking for a passionate and dedicated person to help creating sustainable growth.

As a Tender Manager, you will be responsible for, together with local Tender Managers/Country Leads, driving tender performance for large and strategic public accounts, mainly within EU.

You will engage senior decision makers both internally at Camurus, and externally with payers. Moreover, you will establish, maintain, and expand value partnerships, and position the value and services to these customers through the entire tender/business cycle. Working at Camurus is characterized by teamwork and open communication, and you will work cross-functionally in an international environment.

Main responsibility
Among others, your responsibility will include:

- An important task for the Tender Manager will be to map and keep track of all tender opportunities (both new and prolongations) in the defined tender regions. This includes the responsibility to manage and keep track of hospitals tenders and public procurements through electronic tools etc.
- The Tender Manager will act as a project lead for developing and maintaining a Global Tender dossier that will be adapted locally by local Tender Managers.
- The Tender Manager is expected to influence willingness to pay by delivering evidence-based value proposition and economic quantification of value of Camurus offerings to the stakeholders.
- The Tender Manager will proactively collaborate with colleagues in identifying potential targets and new customers.
- The Tender Manager will map the buyers’ tender processes in order to increase market knowledge.


- The Tender Manager will be consulting Healthcare Professionals (HCPs) and economical buyers on reimbursement, billing, coding, budget impact and financial planning.
- The Tender Manager will be training, and coaching sales functions involved in tendering on value-based engagement.


Candidate profile
We are looking for a senior profile with the following skill set:

- Academic degree or equivalent, together with a commercial or healthcare background
- Good understanding of the pharmaceutical value chain and market environment (local reimbursement systems, budgets and funding flows in hospitals, key decision makers & influencers), or Sales experience in medical devices and/or Pharma environment. Ideally experience from procurement.
- Solid experience in a customer facing role interacting with medical & non-medical staff
- Ability to successfully network in complex cross-functional setting
- Demonstrated ability to analyze and understand market dynamics
- Strategic mindset and strong relationship management skills
- Superior communication, sales & negotiation skills
- Strategic account management skills, and proven understanding of tender & contract process
- Fluency in English (verbal and written)
- Good IT skills, in particular Excel and BI systems
- Structured, organized, and meticulous personality, together with strong analytical skills


The Tender Manager will be based in Lund, and report to the Global Head of Market Access & Pricing.

Camurus offers
This is a great time to join a highly dynamic and innovative company during a very exciting phase of growth. The position offers?an?international work environment and corporate culture, with the possibility for individual development and growth. Camurus?has approximately 170 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 our?ideas?to achieve our?patient-centric vision. This is a full-time permanent 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. For more information about Camurus, please visit: https://www.camurus.com/.

We are looking forward to seeing your application! Visa mindre

BONESUPPORT™ (Nasdaq Stockholm: BONEX) develops and commercializes innovative injectable bio-ceramic bone graft substitutes that remodel to the patient’s own bone and have the capability of eluting drugs. BONESUPPORT’s bone graft substitutes are based on the patented technology platform CERAMENT. The Company is conducting several clinical studies to further demonstrate the clinical and health economic benefits its products deliver and a Premarket Premarket approval filing with the FDA (USA) for CERAMENT G was received in May 2022. The company is based in Lund, Sweden, and the net sales amounted to SEK 181 million in 2020. Please visit www.bonesupport.com (http://www.bonesupport.com) for more information.

The role
As Quality Engineer at BONESUPPORT you are responsible for implementation of new products, components and processes, or changes of the same in the Operations organization. This includes for example to ensure adequate manufacturing documents and specifications in the design documentation (Design History File). You will represent Operations in project teams and change order teams to ensure smooth transfer/design transfer from R&D to Operations, including relevant documents in the DMR (Device Master Record). You will also be responsible for putting together the DHR (Device History Record) and handle the day-to-day batch production release flow. All work is documented in the Quality Management System (MasterControl) and in the ERP system (Navision).

Besides the above mentioned documentation tasks, you will also work with our suppliers, to help implement and organize changes of material, processes or components. Other tasks like root cause investigations, corrective and preventive actions (CAPA) and to solve deviations and non-conformances are also within the role. Additionally, other tasks are within release procedure and quality control. The position involves daily cooperation internally, for example with your colleagues in Operations, QA/RA and R&D, and externally, with our suppliers. You will report to the Director of Operations and will be based in our HQ in Lund.



The profile
We believe you have a university degree within Engineering or as Pharmacist. You have at least 3 years experience from a similar position, preferably from the medical device industry. Most likely, you are today working with quality in close cooperation with R&D and production. It is a strong merit if you are familiar with Design Control and have experience from transferring products from R&D to production. You understand what it means and enjoy working in an international environment and you are process-oriented and you love documentation. High level of English is required, both written and spoken.

At BONESUPPORT we value personal skills as much as professional qualifications, and in this role we are looking for a quality oriented and structured person with good communication skills. Yor are thorough and organized, even meticulous, but still dynamic and pragmatic. It is not the square type of quality person we are looking for - instead you understand other peoples’ situation and you make life easier for people around you. You also like to drive, coordinate and to take ownership of activities. It is important to be able to develop strong working relationships with key stakeholders and to have a positive and ''can do'' attitude!

Why BONESUPPORT?
At BONESUPPORT you will be working together with skilled, dedicated people who enjoy working in a fast growing and innovative organization. You will work in a broad role where you build relationships with colleagues from all departments. We offer a dynamic and stimulating workplace and strive for generating great teamwork, innovation, passion, and performance - which is reflected in impressive employee engagement figures. We believe in our journey and take pride in what we do. In May 2022 Bonesupport got the FDA approval of Cerament G for the US market - which is an enormous commercial success. You can literally feel the positive energy in the company.

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! Visa mindre

BONESUPPORT™ (Nasdaq Stockholm: BONEX) develops and commercializes innovative injectable bio-ceramic bone graft substitutes that remodel to the patient’s own bone and have the capability of eluting drugs. BONESUPPORT’s bone graft substitutes are based on the patented technology platform CERAMENT. The Company is conducting several clinical studies to further demonstrate the clinical and health economic benefits its products deliver and a Premarket approval filing with the FDA (USA) for CERAMENT G is planned in 2022. The company is based in Lund, Sweden, and the net sales amounted to SEK 181 million in 2020. Please visit (http://www.bonesupport.com) for more information.

The role
At Bonesupport we use several partners for manufacturing, production, testing and sterilization of our own products. Your primary task will be to, in close collaboration with our partners, control and plan production and deliveries. New medical technology directives and predicted higher volumes mean higher demands on efficient flow, quality and "output". You will be responsible for contact with suppliers and partners and you will be involved in developing and streamlining the entire production process. This role entails a responsibility to coordinate the continuous work with quality, cost and process improvements at our suppliers. You will have almost daily contact with the supplier in Poland and the position also involves a lot of contacts internally, for example with your colleagues in R&D and Quality.

Other possible tasks:

- Tracking and monitoring performance compared to plan and forecast

- Data-driven in analyzing, optimizing and leaning the supply chain

- Risk evaluation and mitigation of supplier performance variation

- Optimize utilization of resources in the supply chain

You’ll report to Director of Operations and will be based in our HQ in Lund. Trips to Poland occur occasionally, but most tasks are solved by phone and email.

The profile
We believe that you have a solid technical interest, combined with a degree in Engineering. You also have some previous experience, approximately 5-10 years, with similar tasks in med tech and/or pharma industry. You understand what it means and enjoy working in an international environment. Previous work in NAV ERP system is valuable.

At BONESUPPORT we value personal skills as much as professional qualifications, and in this role we are looking for a reliable, quality oriented and structured person with good communication skills, verbally and written. You need to be flexible and able to adjust to current conditions and have strong prioritization and organizational skills with attention to details. It is important to be able to develop strong working relationships with key stakeholders and to have a positive and ''can do'' attitude! High level of English is required.

Why BONESUPPORT?
At BONESUPPORT you will be working together with skilled, dedicated people who enjoy working in a fast growing and innovative organization. We offer a dynamic and stimulating workplace and strive for generating great teamwork, innovation, passion, and performance - which is reflected in impressive employee engagement figures. We believe in our journey and take pride in what we do.



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! Visa mindre