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Validation Specialist BioLife Laboratory Information Management System(m/w/x)
Creating system specifications and conducting qualification testing for BioLife LIMS at a research-based biopharmaceutical company. 1-2 years validation experience in GMP environment with Agile methodology required. Job rotations, mentoring program.
Requirements
- Completed natural scientific or technical education
- At least 1-2 years experience with validation, computerized systems, and/or specifications
- Experience in GMP environment and AGILE methodology
- Very good English language skills
- Good German language skills
- Flexibility and teamwork skills
- Experience in technical and quality documentation
- Analytical thinking and problem solving
- High customer and service orientation
- Independent, precise, and methodical way of working
Tasks
- Create system specifications and key validation documents
- Review and approve validation documents
- Test system functionality
- Manage validation tasks and coordinate resources
- Plan and conduct qualification testing
- Evaluate test results
- Participate in designing Lab Operation processes
- Create system Standard Operating Procedures
Work Experience
- 1 - 2 years
Education
- Vocational certification
Languages
- English – Business Fluent
- German – Basic
Benefits
Bonuses & Incentives
- Attractive annual bonus
Competitive Pay
- Increased payment possible
Learning & Development
- Trainings
Diverse Work
- Job rotations
Mentorship & Coaching
- Mentoring
Family Support
- Balanced work-life ratio
Childcare
- Company kindergarten
Healthcare & Fitness
- Fitness center
Free or Subsidized Food
- Cafeteria
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Validation Specialist BioLife Laboratory Information Management System(m/w/x)
Creating system specifications and conducting qualification testing for BioLife LIMS at a research-based biopharmaceutical company. 1-2 years validation experience in GMP environment with Agile methodology required. Job rotations, mentoring program.
Requirements
- Completed natural scientific or technical education
- At least 1-2 years experience with validation, computerized systems, and/or specifications
- Experience in GMP environment and AGILE methodology
- Very good English language skills
- Good German language skills
- Flexibility and teamwork skills
- Experience in technical and quality documentation
- Analytical thinking and problem solving
- High customer and service orientation
- Independent, precise, and methodical way of working
Tasks
- Create system specifications and key validation documents
- Review and approve validation documents
- Test system functionality
- Manage validation tasks and coordinate resources
- Plan and conduct qualification testing
- Evaluate test results
- Participate in designing Lab Operation processes
- Create system Standard Operating Procedures
Work Experience
- 1 - 2 years
Education
- Vocational certification
Languages
- English – Business Fluent
- German – Basic
Benefits
Bonuses & Incentives
- Attractive annual bonus
Competitive Pay
- Increased payment possible
Learning & Development
- Trainings
Diverse Work
- Job rotations
Mentorship & Coaching
- Mentoring
Family Support
- Balanced work-life ratio
Childcare
- Company kindergarten
Healthcare & Fitness
- Fitness center
Free or Subsidized Food
- Cafeteria
About the Company
Takeda Manufacturing Austria AG
Industry
Pharmaceuticals
Description
Das Unternehmen ist ein weltweit führendes, forschendes biopharmazeutisches Unternehmen, das lebensverbessernde Arzneimittel für komplexe Erkrankungen entwickelt.
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