Novartis Radiopharmaceuticals GmbH
Production Technician / Produktionmitarbeiter(m/w/x)
Full-timeOn-siteExperienced
Halle (Saale)
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NONovartis Radiopharmaceuticals GmbH
Process Expert(m/w/x)
Halle (Saale)
Full-timeOn-siteExperienced
Nejo AI Summary
Driving root cause investigations for product and process issues, ensuring compliant batch manufacturing at a large pharmaceutical manufacturer. 3 years' shop floor process support experience in GMP manufacturing, with compliance investigations, required. On-site manufacturing environment.
Requirements
- Bachelor’s degree in engineering, Pharmacy, Pharmaceutical Technology, Chemistry or relevant experience
- 3 years’ experience in process support shop floor role in GMP manufacturing and/or QA/QC
- Proven process understanding (Pharma, GMP, Regulatory aspects)
- Strong awareness of quality issues
- Compliance investigations experience
- Excellent technical writing skills
- Fluent German and English skills
- Previous Radiopharma experience (advantageous)
- Prior leadership and/or high cross-functional experience (preferred)
Tasks
- Provide front-line manufacturing support.
- Ensure safe and compliant batch manufacturing.
- Act as Subject Matter Expert (SME).
- Serve as first point of contact for product and process issues.
- Drive investigations to root cause.
- Implement corrective and preventive actions (CAPAs).
- Manage and maintain Master Batch Records.
- Manage and maintain Standard Operating Procedures (SOPs).
- Manage and maintain risk assessments and protocols.
- Write and review SOPs, batch records, and white papers.
- Collect data for ongoing process verification (OPV).
- Track and evaluate product performance.
- Support CAPA implementation.
- Author and own material transfer investigations.
- Author and own API synthesis investigations.
- Author and own Drug Substance formulation investigations.
- Author and own Drug product filling investigations.
- Author and own inspection and packaging investigations.
- Ensure processes are inspection-ready.
- Support process optimization and new technology introduction.
- Review validation protocols and reports.
- Support execution of process validations.
- Support short-term improvement projects.
- Guide and support production teams.
- Train and share knowledge with production teams.
- Guide processes to closure and completion.
Work Experience
- 3 years
Education
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Novartis Radiopharmaceuticals 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.
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NONovartis Radiopharmaceuticals GmbH
Process Expert(m/w/x)
Halle (Saale)
Full-timeOn-siteExperienced
Nejo AI Summary
Driving root cause investigations for product and process issues, ensuring compliant batch manufacturing at a large pharmaceutical manufacturer. 3 years' shop floor process support experience in GMP manufacturing, with compliance investigations, required. On-site manufacturing environment.
Requirements
- Bachelor’s degree in engineering, Pharmacy, Pharmaceutical Technology, Chemistry or relevant experience
- 3 years’ experience in process support shop floor role in GMP manufacturing and/or QA/QC
- Proven process understanding (Pharma, GMP, Regulatory aspects)
- Strong awareness of quality issues
- Compliance investigations experience
- Excellent technical writing skills
- Fluent German and English skills
- Previous Radiopharma experience (advantageous)
- Prior leadership and/or high cross-functional experience (preferred)
Tasks
- Provide front-line manufacturing support.
- Ensure safe and compliant batch manufacturing.
- Act as Subject Matter Expert (SME).
- Serve as first point of contact for product and process issues.
- Drive investigations to root cause.
- Implement corrective and preventive actions (CAPAs).
- Manage and maintain Master Batch Records.
- Manage and maintain Standard Operating Procedures (SOPs).
- Manage and maintain risk assessments and protocols.
- Write and review SOPs, batch records, and white papers.
- Collect data for ongoing process verification (OPV).
- Track and evaluate product performance.
- Support CAPA implementation.
- Author and own material transfer investigations.
- Author and own API synthesis investigations.
- Author and own Drug Substance formulation investigations.
- Author and own Drug product filling investigations.
- Author and own inspection and packaging investigations.
- Ensure processes are inspection-ready.
- Support process optimization and new technology introduction.
- Review validation protocols and reports.
- Support execution of process validations.
- Support short-term improvement projects.
- Guide and support production teams.
- Train and share knowledge with production teams.
- Guide processes to closure and completion.
Work Experience
- 3 years
Education
- Bachelor's degree
Languages
- German – Business Fluent
- English – Business Fluent
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Novartis Radiopharmaceuticals 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 Radiopharmaceuticals GmbH
Industry
Pharmaceuticals
Description
Novartis Radiopharmaceuticals GmbH is a manufacturing plant for Radioligand Therapy (RLT) drug products.
Not a perfect match?
- Novartis Radiopharmaceuticals GmbH
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Spezialist Qualitätssicherung in der Produktion(m/w/x)
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Specialist QA CAPA Management(m/w/x)
Full-timeOn-siteExperiencedHalle (Saale) - Simtra BioPharma Solutions
Spezialist Inprozesskontrolle(m/w/x)
Full-timeOn-siteExperiencedHalle (Saale)