Process Manager (IVD Product Development)

Jobdescription

For one of our clients, a world leader in in-vitro

diagnostics, we are currently looking for a Process

Manager.

General

Information : Start

Date :  16.02.2026

Latest Possible Start

Date :  16.03.2026

Planned Employment

Duration :  1 year contract with the possibility of

extension

• Workplace :  Rotkreuz
• Workload :  100%

Home

Office :  possible, less than

50%

Department :  Design Control Excellence

CH (DSRSPC)

Working

Hours :  Standard

About the job :

The Department Design Control

Excellence CH is looking for a process manager with a good

understanding of IVD product development processes. The process

manager is responsible for process guidance, process optimization

and documentation of various development

projects.

The Perfect

Candidate :

Has a university degree in Life

Sciences, Natural Sciences or Engineering as well as first

experience and good technical understanding of product development

processes within a highly regulated environment (working experience

or internship). Database experience and experience in Process

Management is of advantage. Experience in the Diagnostics industry

and experience within the GMP regulated environment is a

plus.

Tasks &

Responsibilities : Responsible for

process guidance, process optimization and documentation of various

development projects (systems and assays) regarding Requirements-

and Risk-Management, Configuration Management, Verification and

Validation Management, defects management and / or Usability

Engineering

Support translation of multi-level

requirements via Requirements Management

process

Conduct detailed risk assessments by

analyzing documents, statistics, reports and market trends and with

a team of cross functional

representatives

Ensure all risks and

requirements are maintained within a database and streamline

approach across projects

Ensure the delivery of

timely and good quality risk and requirements

documentation

Establish and perform

Configuration Management in complex development

projects

Support development projects as

Verification Manager (Planning, Guiding, Training,

Reporting)

Managing project related

interactions with Development, Global Platform Support, Design

Quality Assurance, Regulatory, Medical Affairs, external suppliers

and other internal departments.

Information

gathering from respective stakeholders including consolidation of

information

Independent execution of work

packages within area of responsibility

Organize

and manage their own time within scope of assigned work

packages

Ensure the delivery of timely and good

quality documentation

Must Haves : University degree in

Life Sciences, Natural Sciences or

Engineering

Good technical understanding of

development processes

Excellent verbal and

written communication skills in English, and preferably German in

addition

Database experience

preferred

Experience in Process Management

(Risk- Requirements- Configuration- and / or Verification Management)

or Product Development such as testing is a

plus

First experience in product development in

a highly regulated environment is preferred

(n2H)

Experience in the Diagnostics industry

and experience within the GMP regulated environment is a

plus

Good analytical thinking, a structured,

reliable working manner, ability to prioritize, plan and manage

multiple tasks and to instill a sense of urgency in

teams

Ability to lead by influence,

demonstrated effectiveness, drive decisions and account for

results; ability to resolve conflicts and adapt to change,

effective to drive results and achieve project

goals

Excellent communication and presentation

skills

Open minded team-player with an eye for

details

Ready to drive

global diagnostics forward? Apply now and become an integral part

of this innovative team! We are looking forward to receiving your

application!

Application Submission

Deadline :  20.01.2026