Arcondis is a global consulting company with an exclusive focus on the healthcare and life science industries. Headquartered in Basel, Switzerland, the company has a global footprint with offices in North America, APAC and across Europe. We have been managing challenges and solving problems for our clients in compliance, business processes, information technology, and digital transformation since 2001. Our focus lies in creating value through cross-functional, sophisticated delivery methodologies and intelligent implementation. Our clients love to work with us because of our unique skillsets, our pragmatic approach, and our will to win.
We are a medium-sized international consulting firm dedicated to Life Sciences, with a unique and inspiring culture. Our distinctive culture is the driving force behind our success; it is deeply rooted in our purpose and behaviors.
We are owned by a charitable Foundation; our key differentiator is that we contribute to social causes every year. This ethos is not just a part of our identity; it's our way of life. Our motto, "We make healthcare better," reflects the unwavering commitment we have to improving the lives of people through the work we do.
Our culture fosters collaboration, innovation, and a sense of community that sets us apart from the rest. We are living our values every day. Our leadership is expected to lead by example, demonstrating a dedication to our mission and values.
We embrace diversity and inclusivity, and we believe in giving back to the community. Together, we are not just consultants; we are agents of change, and our culture is the driving force behind our shared purpose.
Medical Office
Consultant Medical Product Excellence
-Contribute to project deliverables and support project leads in Medical Product Excellence engagements
-Execute work packages with guidance across product lifecycle management, regulatory readiness, and validation activities
-Support product lifecycle and regulatory readiness assessments
-Assist in evidence-generation planning, documentation, and analysis
-Contribute to clinical validation activities and technical research
-Apply analytical skills to solve structured problems within defined scope
-Ensure quality and compliance with regulatory and organisational standards
-Perform routine tasks independently with guidance for more complex activities
-Support project-related client interactions and communication
-Build understanding of client needs and regulatory environments
-Apply foundational knowledge in product lifecycle, regulatory, and clinical domains
-Follow established processes, methodologies, and tools
-Support development of templates and tools for clinical, regulatory, and product-related deliverables
-Contribute to internal knowledge management and documentation of project learnings
-Provide feedback on methodologies, tools, and ways of working
-Identify minor process inefficiencies and suggest improvements
-Support project extensions and renewals through high-quality delivery
-Contribute to proposal development and preparation of sales materials
-Provide input based on research, analysis, and project experience
-Develop a professional voice and presence within the organisation
-Maintain a professional personal brand as a subject matter expert in development within Medical Products
-Contribute to internal publications, opinion pieces, and thought leadership content
1
-Master’s or Bachelor’s degree in Life Sciences, Biomedical Engineering, or a related field
-MD or PhD preferred for technical areas
-3–5 years (with a Master’s/Bachelor’s degree) / 1–3 years (with an MD or PhD) of experience in MedTech, regulatory affairs, clinical development, or related areas
-Initial exposure to product lifecycle or regulatory projects is a must
-Understanding of product lifecycle management and regulatory fundamentals
-Working knowledge of medical–regulatory interface and compliance requirements
-Familiarity with FDA and/or EU MDR regulations is preferred
-Foundational understanding of medical device requirements engineering, medical risk analysis, and/or usability engineering.
-Basic knowledge of clinical validation and evidence generation
-Strong analytical skills with the ability to structure and analyse data
-Ability to support problem-solving within defined scope
-Developing structured and systematic thinking
-Strong communication and collaboration skills
-Ability to prepare structured documentation and presentations
-Ability to work effectively in cross-functional and interdisciplinary teams
-Fluent in English
-Ability to manage tasks and deadlines with guidance
-Willingness to learn, seek feedback, and continuously develop skills
-Ability to adapt to new tools, technologies, and regulatory environments
841
Basel, Frankfurt, Kosice, Boston, Singapore, Malaysia
Arcondis is a global consulting company with an exclusive focus on the healthcare and life science industries. Headquartered in Basel, Switzerland, the company has a global footprint with offices in North America, APAC and across Europe. We have been managing challenges and solving problems for our clients in compliance, business processes, information technology, and digital transformation since 2001. Our focus lies in creating value through cross-functional, sophisticated delivery methodologies and intelligent implementation. Our clients love to work with us because of our unique skillsets, our pragmatic approach, and our will to win.
We are a medium-sized international consulting firm dedicated to Life Sciences, with a unique and inspiring culture. Our distinctive culture is the driving force behind our success; it is deeply rooted in our purpose and behaviors.
We are owned by a charitable Foundation; our key differentiator is that we contribute to social causes every year. This ethos is not just a part of our identity; it's our way of life. Our motto, "We make healthcare better," reflects the unwavering commitment we have to improving the lives of people through the work we do.
Our culture fosters collaboration, innovation, and a sense of community that sets us apart from the rest. We are living our values every day. Our leadership is expected to lead by example, demonstrating a dedication to our mission and values.
We embrace diversity and inclusivity, and we believe in giving back to the community. Together, we are not just consultants; we are agents of change, and our culture is the driving force behind our shared purpose.
Medical Office
-Contribute to project deliverables and support project leads in Medical Product Excellence engagements
-Execute work packages with guidance across product lifecycle management, regulatory readiness, and validation activities
-Support product lifecycle and regulatory readiness assessments
-Assist in evidence-generation planning, documentation, and analysis
-Contribute to clinical validation activities and technical research
-Apply analytical skills to solve structured problems within defined scope
-Ensure quality and compliance with regulatory and organisational standards
-Perform routine tasks independently with guidance for more complex activities
-Support project-related client interactions and communication
-Build understanding of client needs and regulatory environments
-Apply foundational knowledge in product lifecycle, regulatory, and clinical domains
-Follow established processes, methodologies, and tools
-Support development of templates and tools for clinical, regulatory, and product-related deliverables
-Contribute to internal knowledge management and documentation of project learnings
-Provide feedback on methodologies, tools, and ways of working
-Identify minor process inefficiencies and suggest improvements
-Support project extensions and renewals through high-quality delivery
-Contribute to proposal development and preparation of sales materials
-Provide input based on research, analysis, and project experience
-Develop a professional voice and presence within the organisation
-Maintain a professional personal brand as a subject matter expert in development within Medical Products
-Contribute to internal publications, opinion pieces, and thought leadership content
1
-Master’s or Bachelor’s degree in Life Sciences, Biomedical Engineering, or a related field
-MD or PhD preferred for technical areas
-3–5 years (with a Master’s/Bachelor’s degree) / 1–3 years (with an MD or PhD) of experience in MedTech, regulatory affairs, clinical development, or related areas
-Initial exposure to product lifecycle or regulatory projects is a must
-Understanding of product lifecycle management and regulatory fundamentals
-Working knowledge of medical–regulatory interface and compliance requirements
-Familiarity with FDA and/or EU MDR regulations is preferred
-Foundational understanding of medical device requirements engineering, medical risk analysis, and/or usability engineering.
-Basic knowledge of clinical validation and evidence generation
-Strong analytical skills with the ability to structure and analyse data
-Ability to support problem-solving within defined scope
-Developing structured and systematic thinking
-Strong communication and collaboration skills
-Ability to prepare structured documentation and presentations
-Ability to work effectively in cross-functional and interdisciplinary teams
-Fluent in English
-Ability to manage tasks and deadlines with guidance
-Willingness to learn, seek feedback, and continuously develop skills
-Ability to adapt to new tools, technologies, and regulatory environments
841
Basel, Frankfurt, Kosice, Boston, Singapore, Malaysia