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Ferrosan Medical Devices sp. z o.o. praca

Ferrosan Medical Devices to innowacyjna firma z siedzibą w Szczecinie, która od ponad siedmiu dekad wyznacza standardy w branży wyposażenia i sprzętu medycznego. Historia przedsiębiorstwa rozpoczęła się od wprowadzenia na rynek rewolucyjnego produktu – SPONGOSTAN™, pierwszej chłonnej gąbki hemostatycznej, która znacząco zmieniła sposób zatrzymywania krwawień podczas operacji.

Zespół składający się z około 100 specjalistów w Ferrosan Medical Devices angażuje się w dostarczanie rozwiązań medycznych, które wspierają ludzi na całym świecie. Pracownicy firmy stawiają na innowacyjność, otwartość oraz tworzenie wartościowych rozwiązań dla swoich partnerów. Każdego dnia dążą do tego, aby ich produkty były synonimem zaufania i skuteczności.

Produkty medyczne do hemostazy i procedur biopsji powstają w wyniku bliskiej współpracy z klinicystami oraz partnerami. W szczególności wyróżnia się wprowadzenie na rynek pierwszego na świecie ręcznego, bezprzewodowego urządzenia do biopsji piersi, które umożliwia jednokrotne wkłucie i pobranie wielu próbek. Ta innowacja ułatwia pracę lekarzy oraz poprawia komfort pacjentów.

Produkty hemostatyczne oferowane przez firmę są doceniane przez profesjonalistów służby zdrowia na całym świecie, co potwierdza międzynarodową obecność Ferrosan Medical Devices oraz zaufanie, jakim obdarzają ją klienci. Każdego dnia dąży do doskonalenia swoich rozwiązań, aby były one jeszcze lepsze, bezpieczniejsze i bardziej dostępne dla potrzebujących.

W Ferrosan Medical Devices łączy się tradycję z nowoczesnością, poszukując sposobów na poprawę jakości życia pacjentów. Dzięki zaangażowaniu oraz pasji zespołu, firma ma nadzieję na wspólne kształtowanie przyszłości medycyny. Zachęca wszystkich do zapoznania się z jej produktami i dołączenia do grona tych, którzy już jej zaufali.

Oferty pracy Ferrosan Medical Devices Sp. z o.o.

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Data aktualizacji: 25.09.2024

Mapa Ferrosan Medical Devices Sp. z o.o.

Siedziba główna

Dane firmy z social mediów (LinkedIn)

Ferrosan Medical Devices

One-stop-shop medical device company

Established in 1947, Ferrosan Medical Devices has been at the forefront of health innovation, developing haemostatic products and diversifying into handheld biopsy devices and electronic medicine pumps. In partnership with Ethicon, Inc (Johnson & Johnson), who expertly handles the marketing and sales of SURGIFLO™, SPONGOSTAN™, and SURGIFOAM®, our products are trusted by healthcare professionals in more than 100 countries. Our central mission revolves around creating solutions for clinical problems within biosurgery. We aim to equip healthcare professionals around the world with innovative therapeutic alternatives that not only enhance their work but also improve patient outcomes. At Ferrosan Medical Devices, our strength lies in our deep clinical insights, research and development, quality management, and operations. We cover all aspects of the product journey, from identifying user needs, developing concepts based on clinical insights, to finally registering and manufacturing the product. We are a close-knit team of 320 employees at our headquarters in Soeborg, near Copenhagen, and 130 in Szczecin, Poland. Our company is experiencing rapid growth, and our team has seen a considerable expansion over recent years. Our employees play a pivotal role in our success story. If our company's journey and vision resonate with you, we invite you to explore our open positions. Follow us to stay updated with Ferrosan Medical Devices!

Miasto
Soeborg
Siedziba główna
Soeborg, Danmark
Branża
Produkcja sprzętu medycznego
Specjalizacje
medical device, manufacturing, product development, innovation, hemostasis, surgery, surgical care, sustainability, electronics, gmp, supply chain, engineering, automation, manufacturing development, technology, biopsy, project management, quality, compliance, biosurgery, haemostasis, hemostatic, haemostatic, flowable, flowables, Spongostan, Surgifoam, Surgiflo i Vetspon

Rok założenia

2010

Liczba pracowników

201-500

Liczba obserwujących

87

Linki

Praca Ferrosan Medical Devices Sp. z o.o. - oferty archiwalne

  • Quality Director

    Ferrosan Medical Devices Sp. z o.o.
    • Szczecin
    • umowa o pracę
    • pełny etat
    • dyrektor/prezes

    • Zakres obowiązków

      The position
      Reporting to the VP, QM&RA in Denmark, the Quality Director will be a part of the Management Team in Poland, while leading a department consisting of 16 FTEs across QA and QC, with a strong focus on ensuring compliance across the organization. The Quality Director position in FeMD offers an exciting and challenging position in an organization with a high degree of interorganizational collaboration and focus on joint effort and commitment. The Director is expected to set a clear direction and provide situational leadership of the QA/QC team. Hence, the role requires strong leadership capabilities of building and coaching a team of highly skilled QA/QC professionals to successfully deliver on targets. The ideal candidate must possess a strategic mindset and be a true team player with a focus on creating an open, inclusive, and collaborative work environment and establishing transparency in the team, possessing a solution-oriented mindset, and easing cross-functional collaboration and interactions between QA/QC and other departments within FeMD. As Quality Director at FeMD, you will:
      • Oversee and manage the whole Quality Department in our Polish facility.
      • Collaborate closely with cross-functional teams to develop and implement comprehensive QA/QC strategies.
        Ensure that the quality management system is maintained and is effective.
      • Report to the management team on the performance of the quality management system and any need for improvement.
      • Ensure the promotion of awareness of regulatory and customer requirements throughout the organization.
        Raise awareness of the need to act in accordance with the appropriate procedures to comply with applicable regulations and / or requirements.
      • Manage internal audits program.
      • Take responsibility for establishing goals, reporting, and continuous improvements in quality factors.
      • Provide employees with clear communication about the company's goals and strategies, explaining their role and underlining the importance of their contribution in achieving specific targets.
      • Work out the departmental budget and monitoring expenditures.
      Consequently, the position calls for an experienced and skilled QA/QC leader, ideally including strong proficiency in working in a medical device company. Additionally, a solution-oriented mindset, superior communication skills and strong stakeholder management capabilities are of the essence.

      Wymagania

      We would like you to meet you if you have:
      • at least 5 years of work experience in the medical device or similar highly regulated industry in the Quality Management area
      • minimum of 5 years of work experience in managerial positions
      • a University Degree
      • excellent English
      • extensive knowledge of quality requirements such as: ISO 13485, QSR 21 CFR Part 820
      • strong analytical skills with ability to define and execute short and long term company strategy
      • experience in performing audits will be an advantage
      • detail-oriented mindset with a passion for identifying opportunities for improvement and translating them into practical solutions.
      • ability to thrive in a fast-paced, evolving environment, embracing the challenges and rewards of our compliance journey.
      • are able to travel occasionally internationally.

      Oferujemy

      What we offer We offer a truly purpose driven workplace with strong roots in values. What exactly this means is quickly visible to our new colleagues. We are driven by improving patient outcomes and we take our values to work every day - we care about each other, our environment and our customers and we win for patients with innovative high-quality solutions. We offer an inclusive workplace with the opportunity to have real impact and a development curve, that you can steepen in the pace, that is suitable to you. You will meet a DK rooted company growing in number of international colleagues and a way of working, where hybrid, digital, learning and innovation are key words. And we take pride in having fun …

  • PROCESS ENGINEER

    Ferrosan Medical Devices Sp. z o.o.
    • Szczecin
    • umowa o pracę
    • pełny etat
    • specjalista (mid/regular)

    • Zakres obowiązków

      Are you a Process Engineer looking for new challenges? Do you possess excellent technical skills, expertise in a manufacturing environment and enjoy daily communication in English? FeMD has an opportunity for you! This position is ideal for a person who is creative and active in proposing new solutions and improvements, taking into account all the rigors resulting from the Quality Management System (QMS) in the medical industry. Responsibilities include:
      • Participation in the development of a new technological process and related equipment
      • Initiating activities to optimize and improve the manufacturing process, solving current problems
      • Recognizing and removing the causes of non-compliance occurring in the production process
      • Participation in validation and revalidation of technological processes
      • Testing and evaluation of technological and product solutions
      • Creation and analysis of process documentation (work instructions, PFMEA, Process Flow)
      • Identification and implementation of actions to prevent losses and production inefficiencies
      • Statistical data analysis

      Wymagania

      Requirements:
      • Technical university degree, preferred mechanical or electrical profile - electrical engineering
      • Very good knowledge of English (B2)
      • Experience in a similar position (minimum 2 years)
      • Good knowledge of production processes and technologies used in the production of mechanical and electrical devices
      • Knowledge of quality and statistical tools
      • Practical knowledge of quality standards in the medical or automotive industry will be a plus
      • Proactive, independent with analytical thinking and problem solving approach
      • Ability to cooperate with employees on all levels, excellent communication skills

      Oferujemy

      What we offer We offer a truly purpose driven workplace with strong roots in values. What exactly this means is quickly visible to our new colleagues. We are driven by improving patient outcomes and we take our values to work every day - we care about each other, our environment and our customers and we win for patients with innovative high-quality solutions. We offer an inclusive workplace with the opportunity to have real impact and a development curve, that you can steepen in the pace, that is suitable to you. You will meet a DK rooted company growing in number of international colleagues and a way of working, where hybrid, digital, learning and innovation are key words. And we take pride in having fun …

  • Data engineer

    Ferrosan Medical Devices Sp. z o.o.
    • Szczecin
    • umowa o pracę
    • pełny etat
    • specjalista (mid/regular)

    • Zakres obowiązków

      More about the roleDo you want to be a part of the IT department in a company with a unique impact on global healthcare? Grab this opportunity to join a rapidly growing company, where we are ready to invest in you. Here you will not only get to impact the production and development of our products; you will also have every opportunity to develop your skills further.Every 3rd second Ferrosan Medical Devices products help surgeons and nurses control bleedings and avoid complications in surgical procedures. We make seconds count in surgical care! And we need you on our team! Send your application along with your CV by January 7, 2024. We will process the applications as we receive them.Questions? Please do not hesitate to contact Director, Group IT, Anders Jacobsen on +45 2929 3300.We look forward to hearing from you. Your responsibilities

      Wymagania

      Our requirements
      • Technologies we use
      Expected
      • Python
      • C#
      • Azure SQL

      Oferujemy

      We are in search of a proficient Data Engineer to become a valuable member of our dynamic team. The ideal candidate should excel in utilizing Azure cloud solutions, be proficient in C# programming, and have a robust ability in documentation, which is crucial for meeting regulatory requirements in the medical device sector. What we offer We offer a truly purpose driven workplace with strong roots in values. What exactly this means is quickly visible to our new colleagues. We are driven by improving patient outcomes and we take our values to work every day - we care about each other, our environment and our customers and we win for patients with innovative high-quality solutions. We offer an inclusive workplace with the opportunity to have real impact and a development curve, that you can steepen in the pace, that is suitable to you. You will meet a DK rooted company growing in number of international colleagues and a way of working, where hybrid, digital, learning and innovation are key words. And we take pride in having fun …

  • System Manager

    Ferrosan Medical Devices Sp. z o.o.
    • Szczecin
    • umowa o pracę
    • pełny etat
    • menedżer

    • Zakres obowiązków

      Role summaryAs our new System Manager in Group IT, you will play a key role influencing our current, as well as our future, production facilities with robust solutions within IT and OT systems and solutions. You will solve your tasks independently as well as in collaboration with professionals with various backgrounds within academics and technical expertise. You will be responsible for managing GxP (GMP) critical IT systems. As part of the IT/OT Compliance team, no days will be the same, as you collaborate with your colleagues to ensure that the documentation for IT and OT solutions are up to date and compliant with both internal and external requirements. This includes risk assessments, requirement specifications, validation, and test documentation as well as periodic reporting. When participating in projects, you will work closely with different stakeholders to assess requirements, design, draw up documentation and test the solutions of our current and future facility. Your core task is to ensure compliance for IT and OT solutions (systems and equipment). Your responsibilities:
      • Ensure stable operation and compliance of IT/OT Systems and drive projects (Implementation and Life Cycle Management). You will ensure systematic and strategic execution of LCM activities.
      • Ensure functionality, documentation, and quality for IT/OT Systems, responsible for systems compliance and support of Systems audits.
      • Prepare and execute Test protocols and Reports.
      • You will perform periodic system evaluation.
      • Ensure good practice of system management, such as Change management, Configuration management, Release management and Incident management.
      Additionally, you will be managing the stakeholders and vendors and understand how to convert the requirements into the desired results.

      Wymagania

      Our requirements: The ideal candidate for this position has:
      • A minimum of 4 years of experience working with documentation of complex systems or processes.
      • A strong Quality/GMP mindset.
      • A bachelor's or master's degree preferably within IT or Automation related fields or an engineering background with a technical flair and curiosity.
      • The ability to handle multiple tasks at once and ensure high quality documentation is delivered timely.
      • Good collaborating and communicating skills as you work closely with a broad variety of key stakeholders, including QC and the production area.
      • Is fluent in technical English
      • Occasional travel to our site in Denmark

      Oferujemy

      What we offer We offer a truly purpose driven workplace with strong roots in values. What exactly this means is quickly visible to our new colleagues. We are driven by improving patient outcomes and we take our values to work every day - we care about each other, our environment and our customers and we win for patients with innovative high-quality solutions. We offer an inclusive workplace with the opportunity to have real impact and a development curve, that you can steepen in the pace, that is suitable to you. You will meet a DK rooted company growing in number of international colleagues and a way of working, where hybrid, digital, learning and innovation are key words. And we take pride in having fun …

  • Kontroler Jakości

    Ferrosan Medical Devices Sp. z o.o.
    • Szczecin
    • umowa o pracę
    • pełny etat
    • młodszy specjalista (junior)

    • Zakres obowiązków

      Zadania:
      • Udział w procesie zwalniania partii produkcyjnej - weryfikacja dokumentacji serii, sprawdzanie poprawności zapisów zgodnie z obowiązującymi w firmie praktykami (GDP - Dobre Praktyki Dokumentacyjne).
      • Codzienny nadzór nad przydzielonymi liniami produkcyjnymi:
        • prowadzenie monitoringu środowiskowego,
        • wyrywkowa kontrola poprawności operacji wykonywanych przez operatorów,
        • pobieranie próbek oraz wykonywanie testów i badań kontrolnych zgodnie z obowiązującą dokumentacją.
      • Współpraca z inżynierami zapewnienia jakości przy rozwiązywaniu bieżących problemów jakościowych oraz przy szkoleniu operatorów.
      • Współpraca przy tworzeniu / aktualizacji dokumentów operacyjnych (instrukcje, formularze, itp.).
      • Udział w procesie obsługi reklamacji

      Wymagania

      Oczekiwania:
      • Wykształcenie: średnie lub wyższe- preferowane techniczne.
      • Doświadczenie: preferowane doświadczenie związane z pracą w firmie produkcyjnej, doświadczenie w pracy na podobnym stanowisku będzie dodatkowym atutem.
      • Znajomość pakietu MS Office (Excel, Word, Outlook).
      • Znajomość języka angielskiego w stopniu dobrym.
      • Podstawowa wiedza z zakresu pomiarów wielkości mechanicznych (długość, wysokość, średnica, siła, itp.) oraz doświadczenie w wykonywaniu pomiarów będą dodatkowym atutem.
      • Porządane cechy:
        • Umiejętność pracy według ściśle określonych procedur.
        • Bardzo dobra organizacja pracy własnej.
        • Samodzielność i skrupulatność w działaniu.
        • Dokładność, spostrzegawczość, dbałość o szczegóły.
        • Nastawienie na pracę zespołową.

      Oferujemy

      • nowoczesne, estetyczne i bezpieczne środowisko pracy w firmie z duńskim kapitałem
      • zatrudnienie na podstawie umowy o pracę
      • stabilność wynagrodzenia, premie oraz nagrody dodatkowe