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Product Steward(m/w/x)
Oversight of entire manufacturing process for pharmaceutical products, acting as technical/scientific support. Strong understanding of GMP, GDP, and validation principles required. Consideration of experience for market position.
Requirements
- Strong understanding of pharmaceutical manufacturing processes and validation principles
- Ability to analyze data trends and apply statistical methods for process control
- Skilled in risk management and Quality Risk Assessment
- Experience in technology transfer and process optimization
- Knowledge of GMP, GDP, and regulatory requirements
- Effective collaboration across functions and global networks
- Problem-solving mindset for complex technical challenges
- Commitment to continuous improvement and operational excellence
- Fluent English language skills
Tasks
- Own process knowledge throughout commercial lifecycle
- Ensure robust, validated, and continuously improving processes
- Maintain oversight of entire manufacturing process
- Act as Single Point of Contact for technical/scientific support
- Create and maintain product-specific Quality Risk Assessments
- Monitor critical process variables using statistical analysis
- Ensure process variables are in control
- Define and implement validation strategies
- Support validation activities
- Coordinate technical transfers and validation batches
- Review Annual Product Quality Reviews
- Adapt control strategies as needed
- Drive harmonization of technical processes
- Optimize technical processes across the site
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Fluent
Benefits
Other Benefits
- Competitive market position
- Consideration of experience, qualifications, and competencies
Diverse Work
- Advice on suitable positions
Mentorship & Coaching
- Guidance at all stages of application process
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Product Steward(m/w/x)
Oversight of entire manufacturing process for pharmaceutical products, acting as technical/scientific support. Strong understanding of GMP, GDP, and validation principles required. Consideration of experience for market position.
Requirements
- Strong understanding of pharmaceutical manufacturing processes and validation principles
- Ability to analyze data trends and apply statistical methods for process control
- Skilled in risk management and Quality Risk Assessment
- Experience in technology transfer and process optimization
- Knowledge of GMP, GDP, and regulatory requirements
- Effective collaboration across functions and global networks
- Problem-solving mindset for complex technical challenges
- Commitment to continuous improvement and operational excellence
- Fluent English language skills
Tasks
- Own process knowledge throughout commercial lifecycle
- Ensure robust, validated, and continuously improving processes
- Maintain oversight of entire manufacturing process
- Act as Single Point of Contact for technical/scientific support
- Create and maintain product-specific Quality Risk Assessments
- Monitor critical process variables using statistical analysis
- Ensure process variables are in control
- Define and implement validation strategies
- Support validation activities
- Coordinate technical transfers and validation batches
- Review Annual Product Quality Reviews
- Adapt control strategies as needed
- Drive harmonization of technical processes
- Optimize technical processes across the site
Work Experience
- approx. 1 - 4 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Fluent
Benefits
Other Benefits
- Competitive market position
- Consideration of experience, qualifications, and competencies
Diverse Work
- Advice on suitable positions
Mentorship & Coaching
- Guidance at all stages of application process
Like this job?
BetaYour Career Agent finds similar jobs for you every day.
About the Company
Novartis Pharmaceutical Manufacturing GmbH
Industry
Pharmaceuticals
Description
The company aims to reimagine medicine to improve and extend people's lives.
Not a perfect match?
- Novartis Pharmaceutical Manufacturing GmbH
Product Steward(m/w/x)
Full-timeOn-siteExperiencedSchaftenaufrom 65,605.64 / year - Novartis Pharmaceutical Manufacturing GmbH
Process Expert(m/w/x)
Full-timeOn-siteExperiencedSchaftenaufrom 59,781.96 / year - Novartis Pharmaceutical Manufacturing GmbH
Technical Transfer Lead(m/w/x)
Full-time/Part-timeOn-siteExperiencedSchaftenaufrom 65,605.54 / year - Novartis Pharmaceutical Manufacturing GmbH
Technical Transfer Lead, Medical Device(m/w/x)
Full-timeOn-siteExperiencedSchaftenaufrom 65,605.54 / year - Novartis Pharmaceutical Manufacturing GmbH
AS&T Expert(m/w/x)
Full-time/Part-timeOn-siteExperiencedSchaftenaufrom 60,600 / year