330 days ago on jobs.prismond.com

Software Validation Engineer

Prismond Group AG

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Software Validation Engineer

Practice:  Medical Devices

Country:  Switzerland

Location: Zurich / Zug

Fast growing Swiss Company

Software Validation Engineer

New kind of Life Science consultancy 

We offer flat hierarchies, consulting with a partnership approach and a close-knit family atmosphere

Multiple and exciting projects

Join a successful and fast growing Life Science consultancy where there is plenty of career growth opportunities

Be involved in a variety of interesting and challenging projects and work within a team; not as an individual

Family atmosphere

Medical Devices (IEC 62304)

Your mission

As the incumbent of this role within Prismond, your challenge will be to guide and support our clients and enabling functions to always do the right thing. This involves being a confident advisor on FDA/EU regulatory compliance (IEC 62304) in Software Development, Documentation, Validation and quality management related topics, in order to achieve timely releases of innovative products that deliver high quality and outstanding reliability to the lives our clients will improve

As the Prismond expert in Software Validation based in Switzerland you have a talent and passion to manage software activities for design, development and manufacturing of medical devices to ensure a high level of process and product quality. You are highly motivated to work in teams and to leverage your expertise into best-practice solutions for our Medical Devices clients

In your role as a Prismond Software Validation Engineer, you are supporting our clients and project teams by:

  • Leading software validation activities for design and development of medical devices to ensure a high level of process and product quality for FDA/EU (IEC 62304)
  • Participating in development of system validation plans to ensure that approach is commensurate with risk assessment
  • Leading our clients in development of use cases and documentation of user requirements
  • Leading development of functional requirements specifications to ensure that requirements are complete, accurate, and testable
  • Developing test strategies and defining test data (i.e. design the approach for testing each requirement)
  • Authoring validation and verification testing protocols/scripts (i.e., IQ, OQ, PQ)
  • Executing validation and verification testing protocols and documenting results
  • Documenting and managing software defects and validation issues, assessments, and resolutions
  • Authoring testing summaries and validation reports
  • Preparing status reports for our clients and management
  • Develop and implement Validation Master Plans

Roles & responsibilities


Focused in Life Science

a dedicated service provider in the medical device, pharma and healthcare industry

Strong Working Culture 

Senior Experts & International Teams

International footprint of teams, subject matter experts and track-record of successful projects

We believe that real consulting starts by bringing more to projects than just bodies. With our deep industry knowledge we develop smart added-value solutions focused on project and personal goals

Prismond at a glance...

Life Science Compliance Services

Strong engaged collaborative style, exceptional and passionate people committed to quality and providing sustainable value

Prismond, is a MedTech, Pharma and Healthcare Service Provider; linking Compliance Services, Product Certification and Commercialization with deep Life Sciences industry knowledge.

We offer our clients lean and sustainable solutions to the most relevant business challenges. Prismond has a strong engaged collaborative style, exceptional and passionate people committed to quality and providing sustainable value to our clients.

Flat hierarchies, advisory services with a partnership approach and a close-knit family atmosphere are essential elements of our company culture. We promote career development and invest in our people.

We have project offices in Zurich, Zug, Lugano, Würzburg, New York and very soon in Hong Kong.

Visit our website for more information:  www.prismond.ch

The Prismond Group

Dedicated Solutions & Tools 

Always Thinking One Step Ahead 

Our motto: to always think one step ahead. What sets us apart and what our clients notice immediately is our curiosity, boldness, sense of responsibility and motivation

What we are looking for

Soft/Consulting skills

  • Master or Bachelor's degree in in computer science, computer engineering/science discipline or technical certification in related field
  • 3-5 years of relevant experience in Software Engineering, Embedded Software or related work experience within Medical Device industry for FDA/EU (IEC 62304)
  • Knowledge of industry and international standards for software quality, such as ISO 13485, IEC 62304, GAMP V, PIC/S, WHO, ICH
  • Regulatory compliance awareness such as GMP, Compliance and Validation Practices including the system development life cycle and regulatory expectations (V-Model)
  • Working experience of validation systems for use in a EMA and FDA regulated environments
  • Experience in technical documentation writing


  • Regulatory compliance awareness including technical file creation / medical device software documentation (IEC 62304) in a regulated industry
  • Strong technical skills with demonstrated ability to provide solutions to a variety of technical problems of moderate scope and complexity
  • Ability to learn quickly and respond to changing priorities
  • Must have strong interpersonal communication skills as well as being a motivated team player
  • Ability to work with global QA, RA, R&D organization
  • Technical writing and presentation skills
  • Good verbal and written communication skills, good team skills including project management
  • Experienced with basic PC skills (MS Word, Excel, PowerPoint, and Project)
  • Excellent oral and technical writing skills in English
  • Strong problem solving skills

Prismond provides three training programs. From the basics through the continuous on project training: before-during-after the project with our SJ coaching program to the ad-hoc specialization with certificates

Prismond Benefits

Partnership approach

All hands

Celebrate together our company wins and other achievement is in our credo. We plan regular events to share relevant updates, welcome our newest hires and host guest speakers

Working for Prismond is fun and challenging at the same time. We provide a nice working environment which includes our trendy project offices, free drinks, a modern working culture, company success participation and above-average social security benefits

Individual training

Apple or Dell

Flat hierarchies, consulting with a partnership approach and a close-knit family atmosphere are essential elements of our company culture

Super Fridays

At Prismond the "Super Friday" culture is celebrated and kept alive. This allows you to see your co-workers regularly outside of ongoing projects

Modern employment package

At Prismond you can choose from day one if you prefer working with an Apple MacBook or a DELL Windows notebook. In addition, we provide all our employees a laptop Re-Buy program

Join our Prismond family

Human Resources, Prismond Group

"The strength of the team is each member. The strength of each member is the team. Our Prismond team looks forward to receiving your CV"

Tina F.

You can differentiate Prismond from the pack. Whether you are a graduate or an experienced professional, if you feel you would thrive in our environment, we would be pleased to hear from you.

Please submit your online application in English or German. For further information, 

please contact our local Human Resources department.

Prismond Group AG (HQ)

Baarerstrasse 10

6304 Zug




Your Application:

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