Validation Specialist (f/m/x) BioLife Laboratory Information Management System - hybrid
応募 後で応募 求人ID R0171088 掲載日 01/09/2026 Location:Vienna, AustriaBy clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.
Job Description
In this challenging role you will be responsible for the implementation and validation of the new global BioLife Laboratory Information Management System. With your pro-active approach and clear communication style, you will act as connector between multiple stakeholders in Lab Operations, IT, Quality and Project Management within our BioLife Europe network.
Your Opportunity:
Creation of system specifications and validation relevant key documents (e.g. Master Validation Plan, Risk Analysis, Incident Reports, Final Report…) for the BioLife Laboratory Information Management System
Review and approval of validation documents
Testing of system functionality
Management of validation tasks, including coordination of internal and/or external resources involved in computerized system validation projects, planning, qualification testing, and evaluation of test results
Participation in design and definition of Lab Operation processes as required by the new BioLife Laboratory Information Management System
Creation of system Standard Operating Procedures
Your Skills and Qualifications:
Completed natural scientific or technical education
Ideally at least 1-2 years experience with validation, computerized systems and/ or specifications
Experience with working in a GMP environment as well as in AGILE methodology beneficial
Very good English language skills required, good German language skills beneficial
Flexible teamplayer with good communication skills
Experience in technical and quality documentation
Analytical thinking and problem solving
High customer and service orientation
Independent, precise and methodical way of working
Hybrid position: 2 days/ week in the office required, the rest of the working time can be managed from homeoffice
This position is limited for 2 years due to project duration. Further long-term opportunities may follow depending on performance and department constellation at the given time.
At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To do this, we empower our people to realize their potential through life-changing work. Takeda encourages and supports its employees by trainings, job rotations and mentoring. A balanced work – life ratio (recognition for work and family, company kindergarten) and numerous benefits (fitness center, cafeteria, etc.) complete our profile as a top employer. For more insights into Takeda click here.
We foster an inclusive, collaborative workplace, in which our global teams are united by an unwavering commitment to deliver Better Health and a Brighter Future to people around the world. Gender, age, skin color, background or sexual orientation play no role in this as we actively promote diversity. We equally address people with disabilities. In the course of a recruitment process which is as free of barriers as possible, we encourage you to mention all relevant information in this context in your application.
Motivated employees must be remunerated accordingly. The minimum salary for this important and responsible position is € 4.270,14 gross/month (full time, collective wage agreement for the chemical industry) plus attractive annual bonus. The actual remuneration package will be guided by your professional experience and your qualifications, so increased payment is possible.