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Senior QA Specialist, DPS (Drug Product Services)(m/w/x)
Description
You will play a pivotal role in ensuring drug product quality by providing shop floor oversight, managing complex quality records, and representing the QA function during critical regulatory audits.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •University degree in Chemistry, Biology, Biotechnology, or related field
- •Long-term experience in pharmaceutical GMP environment
- •Experience in QA department as an advantage
- •Fluent English and advantageous German skills
Education
Work Experience
approx. 4 - 6 years
Tasks
- •Represent Quality Assurance in cross-functional teams
- •Maintain interfaces with manufacturing and engineering teams
- •Execute tasks related to drug product processes
- •Act as the primary contact for manufacturing QA issues
- •Provide dedicated shop floor QA oversight
- •Approve quality records including deviations and CAPAs
- •Review GMP-relevant documents and batch records
- •Present QA topics during customer and regulatory audits
- •Deliver GXP-related trainings to operations personnel
- •Support product-specific and regulatory risk assessments
- •Contribute to continuous improvement of the Quality Management System
Tools & Technologies
Languages
English – Business Fluent
German – Basic
Benefits
Bonuses & Incentives
- •Performance-based compensation programs
Career Advancement
- •Agile career
Informal Culture
- •Dynamic working culture
Purpose-Driven Work
- •Inclusive and ethical workplace
- CH12 Lonza AGFull-timeOn-siteSeniorVisp
- CH12 Lonza AG
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Senior QA Specialist, DPS (Drug Product Services)(m/w/x)
The AI Job Search Engine
Description
You will play a pivotal role in ensuring drug product quality by providing shop floor oversight, managing complex quality records, and representing the QA function during critical regulatory audits.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •University degree in Chemistry, Biology, Biotechnology, or related field
- •Long-term experience in pharmaceutical GMP environment
- •Experience in QA department as an advantage
- •Fluent English and advantageous German skills
Education
Work Experience
approx. 4 - 6 years
Tasks
- •Represent Quality Assurance in cross-functional teams
- •Maintain interfaces with manufacturing and engineering teams
- •Execute tasks related to drug product processes
- •Act as the primary contact for manufacturing QA issues
- •Provide dedicated shop floor QA oversight
- •Approve quality records including deviations and CAPAs
- •Review GMP-relevant documents and batch records
- •Present QA topics during customer and regulatory audits
- •Deliver GXP-related trainings to operations personnel
- •Support product-specific and regulatory risk assessments
- •Contribute to continuous improvement of the Quality Management System
Tools & Technologies
Languages
English – Business Fluent
German – Basic
Benefits
Bonuses & Incentives
- •Performance-based compensation programs
Career Advancement
- •Agile career
Informal Culture
- •Dynamic working culture
Purpose-Driven Work
- •Inclusive and ethical workplace
About the Company
Lonza
Industry
Pharmaceuticals
Description
Lonza is a global leader in life sciences, committed to improving lives through innovative solutions and ethical practices.
- CH12 Lonza AG
Senior QA Specialist(m/w/x)
Full-timeOn-siteSeniorVisp - CH12 Lonza AG
Senior QA Specialist, QA Project Management(m/w/x)
Full-timeOn-siteSeniorVisp - Lonza
Senior QA Specialist/QA Project Manager(m/w/x)
Full-timeOn-siteSeniorVisp - Lonza
Senior QA Specialist, QA Operations(m/w/x)
Full-timeOn-siteSeniorVisp - Lonza
Senior QA Specialist - Product Quality Review(m/w/x)
Full-timeOn-siteSeniorVisp