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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
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
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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