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Investigation Specialist(m/w/x)
Description
As an Investigation Specialist, you will focus on optimizing manufacturing processes and managing critical deviations. This role involves driving impactful changes and ensuring compliance with GMP standards in a sterile environment.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Bachelor's or Master's Degree in Pharmaceutical Technology, Chemistry, Pharmacy, or equivalent work experience
- •At least one year of experience in Sterile Manufacturing in operations and/or QC/QA
- •Previous experience with investigation/deviation management in TW and CAPA definition
- •Proficiency in English; German is an advantage
- •Familiarity with GMP requirements, quality procedures, and SOP execution
- •Good interpersonal skills with various interfaces within the organization and shopfloor
- •Structured, focused, proactive, and well-organized working demeanor
- •High motivation and collaboration focus; oriented towards finding solutions and driven by science
Education
Work Experience
1 year
Tasks
- •Drive optimization projects for manufacturing processes
- •Own investigations and critical deviations
- •Assist in decision-making on production issues
- •Implement process changes and CAPAs
- •Conduct CAPA efficiency checks within required timelines
- •Utilize GMP systems like Trackwise, SAP, and MES
- •Perform retraining and awareness sessions as needed
Languages
English – Business Fluent
German – Basic
Benefits
Bonuses & Incentives
- •Compensation programs for high performance
Corporate Discounts
- •Numerous lifestyle benefits
- •Leisure benefits
Family Support
- •Family benefits
Other Benefits
- •Relocation assistance
- CH12 Lonza AGFull-timeOn-siteExperiencedVisp
- CH12 Lonza AG
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Investigation Specialist(m/w/x)
The AI Job Search Engine
Description
As an Investigation Specialist, you will focus on optimizing manufacturing processes and managing critical deviations. This role involves driving impactful changes and ensuring compliance with GMP standards in a sterile environment.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Bachelor's or Master's Degree in Pharmaceutical Technology, Chemistry, Pharmacy, or equivalent work experience
- •At least one year of experience in Sterile Manufacturing in operations and/or QC/QA
- •Previous experience with investigation/deviation management in TW and CAPA definition
- •Proficiency in English; German is an advantage
- •Familiarity with GMP requirements, quality procedures, and SOP execution
- •Good interpersonal skills with various interfaces within the organization and shopfloor
- •Structured, focused, proactive, and well-organized working demeanor
- •High motivation and collaboration focus; oriented towards finding solutions and driven by science
Education
Work Experience
1 year
Tasks
- •Drive optimization projects for manufacturing processes
- •Own investigations and critical deviations
- •Assist in decision-making on production issues
- •Implement process changes and CAPAs
- •Conduct CAPA efficiency checks within required timelines
- •Utilize GMP systems like Trackwise, SAP, and MES
- •Perform retraining and awareness sessions as needed
Languages
English – Business Fluent
German – Basic
Benefits
Bonuses & Incentives
- •Compensation programs for high performance
Corporate Discounts
- •Numerous lifestyle benefits
- •Leisure benefits
Family Support
- •Family benefits
Other Benefits
- •Relocation assistance
About the Company
CH12 Lonza AG
Industry
Pharmaceuticals
Description
The company is a global leader in life sciences, dedicated to improving lives through innovative solutions.
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