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randstad sweden group ab has its registered office in solna, sweden, with registration number 556089-6572.
our head office is located at rättarvägen 3, box 3037, 169 03 solna.
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  • project manager medtech

project manager medtech

apply
  • gothenburg, vastra gotaland
  • posted 16 october 2025
last day to apply 30 november 2025

job details

last day to apply 30 november 2025

summary

  • gothenburg, vastra gotaland
  • contingent
  • full-time
posted 16 october 2025
    number of offers
    1
  • reference number
    JN -102025-531933

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    randstad professional

    randstad professional

    we bring diverse and pre qualified professional talent and businesses together to connect the right people with the right roles. by building specialized teams, we help individuals flourish in their careers and businesses succeed.

    job details

    Are you an expert navigator who can steer complex projects from initial concept through to market launch? Do you have a passion for Life Science and a track record of successfully delivering innovative medical device solutions? We are seeking a dynamic and results-driven Project Manager to join our team in Gothenburg and lead critical initiatives that enhance patient care globally. Our customer is a major global player in advanced medical solutions, dedicated to developing products that lead to better patient and economic outcomes, who offers a stimulating, collaborative international environment where your expertise directly translates into life-changing products.


    ...

    About the role:

    As a Project Manager focused on product development, you will be the central force coordinating multi-disciplinary teams across R&D, Clinical, Regulatory, Manufacturing, and Marketing. Your primary focus will be on ensuring projects are delivered on time, within budget, and meet all defined performance and quality targets within the regulated MedTech environment.


    Who you are:

    You are a natural leader with exceptional organizational skills and a deep understanding of the scientific and technical challenges inherent in MedTech development. You thrive in a global environment and possess the ability to motivate teams and drive alignment towards a common goal.


    This is a consulting assignment within Randstad Life Sciences which is specializing in competences within Life Science. As a consultant with us, you get a competitive salary, benefits and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.


    If you are ready to make a difference and join our customer exciting growth journey, apply before the 30th of November 2025. Selection and interviews will be ongoing. The starting date will be agreed upon by all parties.

    show more

    Are you an expert navigator who can steer complex projects from initial concept through to market launch? Do you have a passion for Life Science and a track record of successfully delivering innovative medical device solutions? We are seeking a dynamic and results-driven Project Manager to join our team in Gothenburg and lead critical initiatives that enhance patient care globally. Our customer is a major global player in advanced medical solutions, dedicated to developing products that lead to better patient and economic outcomes, who offers a stimulating, collaborative international environment where your expertise directly translates into life-changing products.


    About the role:

    As a Project Manager focused on product development, you will be the central force coordinating multi-disciplinary teams across R&D, Clinical, Regulatory, Manufacturing, and Marketing. Your primary focus will be on ensuring projects are delivered on time, within budget, and meet all defined performance and quality targets within the regulated MedTech environment.

    ...

    Who you are:

    You are a natural leader with exceptional organizational skills and a deep understanding of the scientific and technical challenges inherent in MedTech development. You thrive in a global environment and possess the ability to motivate teams and drive alignment towards a common goal.


    This is a consulting assignment within Randstad Life Sciences which is specializing in competences within Life Science. As a consultant with us, you get a competitive salary, benefits and collective agreements. Your consultant manager is always there for you and ensures that you get varying and developing assignments at different companies, within different industries. At Randstad Life Sciences, your personal development is in focus, and you are offered a large network and many social activities.


    If you are ready to make a difference and join our customer exciting growth journey, apply before the 30th of November 2025. Selection and interviews will be ongoing. The starting date will be agreed upon by all parties.

    show more
    • qualification

      • Bachelor's or Master's degree in a relevant Life Science or Engineering discipline (e.g., Biomedical Engineering, Chemical Engineering).
      • Minimum of 5 years of experience managing complex projects, with at least 3 years directly within the Medical Device (MedTech) industry.
      • Proven expertise in applying Design Control processes and phase-gate methodologies for new product introduction (NPI).
      • Strong knowledge of global medical device regulations (e.g., ISO 13485, MDR/FDA requirements).
      • Excellent leadership, negotiation, and stakeholder management skills.
      • Project Management certification (e.g., PMP, PRINCE2) is highly desirable.
      • Fluent in English (both written and spoken).
    • key responsibilities

      • Lead cross-functional project teams through the entire product development lifecycle, ensuring adherence to Design Control procedures.
      • Develop, maintain, and manage comprehensive project plans, including scope, schedule, budget, resources, and risk management.
      • Drive project execution, proactively identifying and resolving roadblocks and managing dependencies between various functional groups.
      • Facilitate effective communication and decision-making among all stakeholders, providing clear and regular status updates to senior management.
      • Ensure all project deliverables comply with applicable regulatory requirements (e.g., ISO 13485, FDA regulations, EU MDR) and internal quality standards.
      • Champion best practices in project management (e.g., phase-gate models) and drive continuous improvement within the development process.