Immatics Biotechnologies GmbH
GCP/ GCLP Auditor as Senior Manager Clinical Quality Assurance(m/w/x)
Full-time/Part-timeWith HomeofficeSenior
Tübingen, München
New Job?Nejo!
The AI Job Search Engine
BABavarian Nordic GmbH
Senior Quality Assurance Specialist - GVP(m/w/x)
Martinsried
Full-timeRemoteSenior
Nejo AI Summary
Leading pharmacovigilance audits and regulatory inspections for life-saving vaccine development. 7 years pharma/biotech and 5 years QA experience, with pharmacovigilance audit experience required. Flexible work options.
Requirements
- Determination to make things happen
- University degree in natural sciences or comparable qualification
- 7 years pharmaceutical or biotech experience
- 5 years quality assurance experience
- Experience conducting pharmacovigilance audits
- Knowledge of GCP (beneficial)
- Experience preparing and hosting regulatory inspections
- Knowledge of applied risk management
- Experience in managing projects
- Strong analytical, problem-solving and decision-making skills
- Fluency in English
- Knowledge of German (beneficial)
- Initiative and ownership
- Proactive and solution-oriented mindset
- Ability to work independently
- Strong communication skills
- Ability to maintain effective relationships
Tasks
- Support corporate pharmacovigilance audit programs
- Oversee subcontracted audit activities
- Lead internal and external pharmacovigilance audits
- Prepare for and host regulatory inspections
- Manage audits conducted by business partners
- Support quality oversight for pharmacovigilance
- Track change controls and investigations to closure
- Manage deviations and CAPA processes
- Develop and improve the Quality Management System
Work Experience
- 7 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Basic
Tools & Technologies
- GCP
Benefits
Flexible Working
- Inclusive and flexible workplace
Learning & Development
- Personal and professional development
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Bavarian Nordic 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?
- Denk Pharma GmbH & Co. KG
Manager Quality Assurance GMP - Systems & Compliance(m/w/x)
Full-timeTemporary contractWith HomeofficeExperiencedMünchen - NanoTemper Technologies
Senior Quality Expert - CSV(m/w/x)
Full-timeWith HomeofficeSeniorMünchen - Sobi
Global Product Safety Science Lead(m/w/x)
Full-timeRemoteSeniorMünchen - PSI CRO
Senior / Clinical Research Associate(m/w/x)
Full-timeWith HomeofficeSeniorMünchen
BABavarian Nordic GmbH
Senior Quality Assurance Specialist - GVP(m/w/x)
Martinsried
Full-timeRemoteSenior
Nejo AI Summary
Leading pharmacovigilance audits and regulatory inspections for life-saving vaccine development. 7 years pharma/biotech and 5 years QA experience, with pharmacovigilance audit experience required. Flexible work options.
Requirements
- Determination to make things happen
- University degree in natural sciences or comparable qualification
- 7 years pharmaceutical or biotech experience
- 5 years quality assurance experience
- Experience conducting pharmacovigilance audits
- Knowledge of GCP (beneficial)
- Experience preparing and hosting regulatory inspections
- Knowledge of applied risk management
- Experience in managing projects
- Strong analytical, problem-solving and decision-making skills
- Fluency in English
- Knowledge of German (beneficial)
- Initiative and ownership
- Proactive and solution-oriented mindset
- Ability to work independently
- Strong communication skills
- Ability to maintain effective relationships
Tasks
- Support corporate pharmacovigilance audit programs
- Oversee subcontracted audit activities
- Lead internal and external pharmacovigilance audits
- Prepare for and host regulatory inspections
- Manage audits conducted by business partners
- Support quality oversight for pharmacovigilance
- Track change controls and investigations to closure
- Manage deviations and CAPA processes
- Develop and improve the Quality Management System
Work Experience
- 7 years
Education
- Bachelor's degree
Languages
- English – Business Fluent
- German – Basic
Tools & Technologies
- GCP
Benefits
Flexible Working
- Inclusive and flexible workplace
Learning & Development
- Personal and professional development
Find the original job posting in its most current version here. Nejo automatically captured this job from the website of Bavarian Nordic 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
Bavarian Nordic GmbH
Industry
Pharmaceuticals
Description
The company is a global leader in developing life-saving vaccines with over 30 years of experience.
Not a perfect match?
- Immatics Biotechnologies GmbH
GCP/ GCLP Auditor as Senior Manager Clinical Quality Assurance(m/w/x)
Full-time/Part-timeWith HomeofficeSeniorTübingen, München - Denk Pharma GmbH & Co. KG
Manager Quality Assurance GMP - Systems & Compliance(m/w/x)
Full-timeTemporary contractWith HomeofficeExperiencedMünchen - NanoTemper Technologies
Senior Quality Expert - CSV(m/w/x)
Full-timeWith HomeofficeSeniorMünchen - Sobi
Global Product Safety Science Lead(m/w/x)
Full-timeRemoteSeniorMünchen - PSI CRO
Senior / Clinical Research Associate(m/w/x)
Full-timeWith HomeofficeSeniorMünchen