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(Senior) Manager – Quality operations and Deputy Responsible Person (RP)(m/w/x)
Description
In this role, you will ensure compliance with regulations for Medicinal Products while managing quality tasks and supporting GMP activities. Your day-to-day responsibilities will involve overseeing quality processes, conducting audits, and contributing to continuous improvement efforts.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •BA/BS, MA/MS in scientific discipline or related field
- •5 years’ experience in Quality function in pharmaceutical industry
- •Strong understanding of GMPs, GDP, ICH guidelines
- •Significant experience as lead auditor for pharmaceutical manufacturing
- •Experience with regulatory agencies such as Swissmedic, EMA, FDA
- •Prior experience as deputy Responsible Person & interactions with Swissmedic
- •Fluency in English; German and/or French beneficial
- •Ability to work effectively in team-oriented environment
- •Leadership, Drive, Enthusiasm skills
- •Goal-Orientated and commitment to follow up on tasks
- •Decision Making, Problem Solving, Independence skills
- •Flexibility and willingness to travel (up to approx. 25%)
- •Proactive and Self-motivated
Education
Work Experience
5 years
Tasks
- •Manage GDP-related quality tasks
- •Support GMP activities for trading Medicinal Products
- •Maintain knowledge of cGxP regulations and applicable standards
- •Implement requirements into local procedures
- •Act as deputy Responsible Person (RP)
- •Support GxP activities for commercial medicinal products
- •Contribute to maintenance of Quality Systems for Swissmedic licenses
- •Support due diligence and supplier qualification activities
- •Manage Quality Agreements and conduct audits
- •Oversee collection and processing of Events, Changes, and CAPAs
- •Notify management of events requiring immediate action
- •Develop and collect Key Quality/Compliance Indicators
- •Contribute to continuous improvement of quality processes
- •Identify training needs for the BU Pharma & Nutrition team
- •Contribute to internal audits and Health Authorities inspections
- •Support quality oversight of C(D)MOs and Testing Labs
- •Manage Quality Management Reviews for BU Pharma & Nutrition
Languages
English – Business Fluent
German – Basic
French – Basic
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(Senior) Manager – Quality operations and Deputy Responsible Person (RP)(m/w/x)
The AI Job Search Engine
Description
In this role, you will ensure compliance with regulations for Medicinal Products while managing quality tasks and supporting GMP activities. Your day-to-day responsibilities will involve overseeing quality processes, conducting audits, and contributing to continuous improvement efforts.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •BA/BS, MA/MS in scientific discipline or related field
- •5 years’ experience in Quality function in pharmaceutical industry
- •Strong understanding of GMPs, GDP, ICH guidelines
- •Significant experience as lead auditor for pharmaceutical manufacturing
- •Experience with regulatory agencies such as Swissmedic, EMA, FDA
- •Prior experience as deputy Responsible Person & interactions with Swissmedic
- •Fluency in English; German and/or French beneficial
- •Ability to work effectively in team-oriented environment
- •Leadership, Drive, Enthusiasm skills
- •Goal-Orientated and commitment to follow up on tasks
- •Decision Making, Problem Solving, Independence skills
- •Flexibility and willingness to travel (up to approx. 25%)
- •Proactive and Self-motivated
Education
Work Experience
5 years
Tasks
- •Manage GDP-related quality tasks
- •Support GMP activities for trading Medicinal Products
- •Maintain knowledge of cGxP regulations and applicable standards
- •Implement requirements into local procedures
- •Act as deputy Responsible Person (RP)
- •Support GxP activities for commercial medicinal products
- •Contribute to maintenance of Quality Systems for Swissmedic licenses
- •Support due diligence and supplier qualification activities
- •Manage Quality Agreements and conduct audits
- •Oversee collection and processing of Events, Changes, and CAPAs
- •Notify management of events requiring immediate action
- •Develop and collect Key Quality/Compliance Indicators
- •Contribute to continuous improvement of quality processes
- •Identify training needs for the BU Pharma & Nutrition team
- •Contribute to internal audits and Health Authorities inspections
- •Support quality oversight of C(D)MOs and Testing Labs
- •Manage Quality Management Reviews for BU Pharma & Nutrition
Languages
English – Business Fluent
German – Basic
French – Basic
About the Company
206030 Fresenius Kabi SwissBioSim GmbH
Industry
Pharmaceuticals
- Becton, Dickinson and Company
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