Dietrich engineering consultants S.A.
Validation & Documentation Engineer – 100%
Ecublens
80%-100%
Full-time
Technisch
Maschinen- / Anlagenbau / Produktion
Validation & Documentation Engineer (M/F/X) – 100% Following recent acquisitions, Dec Group continues to accelerate its growth and expands its product range, particularly in the field of aseptic and containment filling l…
Details
Validation & Documentation Engineer (M/F/X) – 100%
Following recent acquisitions, Dec Group continues to accelerate its growth and expands its product range, particularly in the field of aseptic and containment filling lines and Isolators. As a leader in the design and production of powder transfer, handling and containment equipment for pharmaceutical and Chemical industries, Dec Group offers global solutions throughout the production chain from the raw material handling to the final product packaging process. The group has more than 950 employees worldwide, including 120 employees headquartered in Switzerland.
For our Headquarters in Ecublens and the Cheseaux office, we are looking for a:
Validation & Documentation Engineer (M/F/X) – 100%
Your role:
Working with DEC Project Managers and Customers, providing support and assistance for all qualification and validation services – writing test protocols and test execution.
Working with DEC Global Qualification & Validation manager & Project Quality Manager to update and maintain global templates, instructions and documentation for validation & documentation to support implementation to DEC global subsidiaries.
To support the DEC Sales team to analyse customer User Requirement Specifications and advise relevant documentation & testing services required and/or to be proposed with DEC offers
Role can be customer facing, during test execution and project meetings.
Your profile:
Previous validation or commissioning/testing experience, in highly regulated industry
Well-organized and can work independently in daily tasks.
High level of technical documentation skills and attention to detail.
Good team working
Excellent French and English level (minimum B2)
Good IT skills
Advanced technical degree qualified, preferably chemical / process / quality engineering
Proven experience in pharmaceuticals – design and/or manufacturing.
Ability / Willingness to travel where necessary – to other subsidiaries, to customers mainly in Europe but could also be worldwide.
Potentially up to 50% travel, depending on project requirements.
Start date: immediately or to be determined
Have we piqued your interest? Feel free to send us your complete application through the JobUP platform.
We will only respond to applications that match the required profile. jidc80cdc9sy jit0626sy jiy26sy
Following recent acquisitions, Dec Group continues to accelerate its growth and expands its product range, particularly in the field of aseptic and containment filling lines and Isolators. As a leader in the design and production of powder transfer, handling and containment equipment for pharmaceutical and Chemical industries, Dec Group offers global solutions throughout the production chain from the raw material handling to the final product packaging process. The group has more than 950 employees worldwide, including 120 employees headquartered in Switzerland.
For our Headquarters in Ecublens and the Cheseaux office, we are looking for a:
Validation & Documentation Engineer (M/F/X) – 100%
Your role:
Working with DEC Project Managers and Customers, providing support and assistance for all qualification and validation services – writing test protocols and test execution.
Working with DEC Global Qualification & Validation manager & Project Quality Manager to update and maintain global templates, instructions and documentation for validation & documentation to support implementation to DEC global subsidiaries.
To support the DEC Sales team to analyse customer User Requirement Specifications and advise relevant documentation & testing services required and/or to be proposed with DEC offers
Role can be customer facing, during test execution and project meetings.
Your profile:
Previous validation or commissioning/testing experience, in highly regulated industry
Well-organized and can work independently in daily tasks.
High level of technical documentation skills and attention to detail.
Good team working
Excellent French and English level (minimum B2)
Good IT skills
Advanced technical degree qualified, preferably chemical / process / quality engineering
Proven experience in pharmaceuticals – design and/or manufacturing.
Ability / Willingness to travel where necessary – to other subsidiaries, to customers mainly in Europe but could also be worldwide.
Potentially up to 50% travel, depending on project requirements.
Start date: immediately or to be determined
Have we piqued your interest? Feel free to send us your complete application through the JobUP platform.
We will only respond to applications that match the required profile. jidc80cdc9sy jit0626sy jiy26sy
