Novartis Pharmaceutical Manufacturing GmbH
QA Specialist Operations(m/w/x)
Full-time/Part-timeWith HomeofficeExperienced
Kundl
from 58,199.96 / year
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NONovartis Pharmaceutical Manufacturing GmbH
QA Specialist Operations(m/w/x)
Kundl
from 59,781.96 / year
Full-time, Part-timeWith Home OfficeExperienced
Nejo AI Summary
Managing GxP compliance for raw materials and consumables in SAP master data systems. QC/QA experience in pharmaceutical/biotech with environmental monitoring required. Childcare facilities, worldwide career possibilities.
Requirements
- Experience in QC/QA in pharmaceutical industry or biotech with environmental monitoring
- Experience with GMP procedures, QA, and QC testing
- Technological expertise and intelligence
- Ability to deal with ambiguity
- Continuous learning
- Collaboration across boundaries
- English and German language skills
- Self-awareness
Tasks
- Manage quality aspects and projects
- Ensure GxP conformity and compliance
- Support CP implementation in SAP and master data systems
- Assist with QA master data topics for raw materials and consumables
- Create master data sheets and collect information
- Participate in projects and troubleshoot master data issues
- Address master data-related non-conformities for raw materials and consumables
- Evaluate changes and support PEM for master data topics
- Assist in creating and collecting CoAs for raw materials and consumables
- Support stability studies and master data maintenance
- Troubleshoot master data issues with connected units
Work Experience
- approx. 1 - 4 years
Education
- Vocational certificationOR
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- German – Business Fluent
Benefits
Bonuses & Incentives
- Attractive incentive program
Retirement Plans
- Modern company pension scheme
Childcare
- Childcare facilities
Learning & Development
- Learning and development opportunities
Career Advancement
- Worldwide career possibilities
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Novartis Pharmaceutical Manufacturing GmbH and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
Not a perfect match?
- Novartis
QA Operations Expert(m/w/x)
Full-time/Part-timeWith HomeofficeExperiencedSchaftenaufrom 65,605.54 / year - Novartis Pharmaceutical Manufacturing GmbH
QA Operations Expert(m/w/x)
Full-time/Part-timeWith HomeofficeExperiencedSchaftenaufrom 65,605.54 / year - Novartis Pharmaceutical Manufacturing GmbH
Senior QA Compliance Specialist(m/w/x)
Full-time/Part-timeWith HomeofficeSeniorSchaftenaufrom 59,781 / year - Novartis
QA Compliance Expert(m/w/x)
Full-timeWith HomeofficeExperiencedSchaftenaufrom 64,023.54 / year
NONovartis Pharmaceutical Manufacturing GmbH
QA Specialist Operations(m/w/x)
Kundl
from 59,781.96 / year
Full-time, Part-timeWith Home OfficeExperienced
Nejo AI Summary
Managing GxP compliance for raw materials and consumables in SAP master data systems. QC/QA experience in pharmaceutical/biotech with environmental monitoring required. Childcare facilities, worldwide career possibilities.
Requirements
- Experience in QC/QA in pharmaceutical industry or biotech with environmental monitoring
- Experience with GMP procedures, QA, and QC testing
- Technological expertise and intelligence
- Ability to deal with ambiguity
- Continuous learning
- Collaboration across boundaries
- English and German language skills
- Self-awareness
Tasks
- Manage quality aspects and projects
- Ensure GxP conformity and compliance
- Support CP implementation in SAP and master data systems
- Assist with QA master data topics for raw materials and consumables
- Create master data sheets and collect information
- Participate in projects and troubleshoot master data issues
- Address master data-related non-conformities for raw materials and consumables
- Evaluate changes and support PEM for master data topics
- Assist in creating and collecting CoAs for raw materials and consumables
- Support stability studies and master data maintenance
- Troubleshoot master data issues with connected units
Work Experience
- approx. 1 - 4 years
Education
- Vocational certificationOR
- Bachelor's degreeOR
- Master's degree
Languages
- English – Business Fluent
- German – Business Fluent
Benefits
Bonuses & Incentives
- Attractive incentive program
Retirement Plans
- Modern company pension scheme
Childcare
- Childcare facilities
Learning & Development
- Learning and development opportunities
Career Advancement
- Worldwide career possibilities
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Novartis Pharmaceutical Manufacturing GmbH and processed the information on Nejo with the help of AI for you. Despite careful analysis, some information may be incomplete or inaccurate. Please always verify all details in the original posting! Content and copyrights of the original posting belong to the advertising company.
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
QA Specialist Operations(m/w/x)
Full-time/Part-timeWith HomeofficeExperiencedKundlfrom 58,199.96 / year - Novartis
QA Operations Expert(m/w/x)
Full-time/Part-timeWith HomeofficeExperiencedSchaftenaufrom 65,605.54 / year - Novartis Pharmaceutical Manufacturing GmbH
QA Operations Expert(m/w/x)
Full-time/Part-timeWith HomeofficeExperiencedSchaftenaufrom 65,605.54 / year - Novartis Pharmaceutical Manufacturing GmbH
Senior QA Compliance Specialist(m/w/x)
Full-time/Part-timeWith HomeofficeSeniorSchaftenaufrom 59,781 / year - Novartis
QA Compliance Expert(m/w/x)
Full-timeWith HomeofficeExperiencedSchaftenaufrom 64,023.54 / year