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Senior QA Operations Expert; Qualified Person(m/w/x)
Certifying and releasing secondary packed drug product batches for commercial purposes at a pharmaceutical manufacturing site. Proven experience in Audit and Inspection Management required. 4-day work week, company car for private use.
Requirements
- Proven experience in Audit and Inspection Management
- Strong working knowledge of cGMP and GxP requirements
- Hands-on experience with Release Management and batch disposition
- Solid expertise in Quality Management Systems (QMS), Quality Assurance, and Quality Compliance
- Background in Technical Operations with technological aptitude
- Demonstrated people leadership capability
- Sound decision-making in patient-focused environment
- Strong collaboration skills
- Strong communication skills
- Strong problem-solving skills
- Ability to navigate ambiguity effectively
- High commitment to data integrity
- Digital proficiency
- Audit & Inspection Management experience
- Good Manufacturing Practices (cGMP) knowledge
- Release Management experience
- Quality Management Systems knowledge
- Technical Operations experience
- GxP Experience
- People Management experience
- Quality Assurance knowledge
- Quality Compliance knowledge
- Technological Expertise
- Patient Safety focus
- Collaboration skills
- Regulatory requirements knowledge
- Dealing with ambiguity
- Problem Solving Skills
- Communication skills
- Data Integrity commitment
- Digital saviness
- Leadership skills
- Decision Making skills
Tasks
- Certify and release secondary packed drug product batches for commercial purposes
- Ensure compliance with AMG, Marketing Authorization, and GMP requirements
- Verify product quality and documentation for batch release
- Lead critical negotiations with internal and external stakeholders
- Provide coaching, performance management, and capability building
- Manage technical operations and provide day-to-day quality support
- Collaborate across functions to align on priorities, risks, and delivery commitments
- Participate in escalations, recalls, and critical complaint investigations
- Evaluate process changes and deviations
- Plan and deliver projects to agreed quality, scope, and timelines
- Ensure inspection and audit readiness
- Coordinate responses and drive timely, sustainable CAPAs
- Support preparation for and participation in audits and inspections
- Maintain and improve Quality Management System processes
- Oversee release management activities
- Report technical complaints, adverse events, and special case scenarios within 24 hours
- Coordinate distribution of marketing samples as needed
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Native
Tools & Technologies
- cGMP
- GxP
- QMS
Not a perfect match?
- NovartisFull-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
QA Specialist Operations(m/w/x)
Full-time/Part-timeWith HomeofficeExperiencedKundlfrom 58,199.96 / year - Novartis
QA Compliance Expert(m/w/x)
Full-timeWith HomeofficeExperiencedSchaftenaufrom 64,023.54 / year - Novartis Pharmaceutical Manufacturing GmbH
QA Specialist Operations(m/w/x)
Full-time/Part-timeWith HomeofficeExperiencedKundlfrom 59,781.96 / year
Senior QA Operations Expert; Qualified Person(m/w/x)
Certifying and releasing secondary packed drug product batches for commercial purposes at a pharmaceutical manufacturing site. Proven experience in Audit and Inspection Management required. 4-day work week, company car for private use.
Requirements
- Proven experience in Audit and Inspection Management
- Strong working knowledge of cGMP and GxP requirements
- Hands-on experience with Release Management and batch disposition
- Solid expertise in Quality Management Systems (QMS), Quality Assurance, and Quality Compliance
- Background in Technical Operations with technological aptitude
- Demonstrated people leadership capability
- Sound decision-making in patient-focused environment
- Strong collaboration skills
- Strong communication skills
- Strong problem-solving skills
- Ability to navigate ambiguity effectively
- High commitment to data integrity
- Digital proficiency
- Audit & Inspection Management experience
- Good Manufacturing Practices (cGMP) knowledge
- Release Management experience
- Quality Management Systems knowledge
- Technical Operations experience
- GxP Experience
- People Management experience
- Quality Assurance knowledge
- Quality Compliance knowledge
- Technological Expertise
- Patient Safety focus
- Collaboration skills
- Regulatory requirements knowledge
- Dealing with ambiguity
- Problem Solving Skills
- Communication skills
- Data Integrity commitment
- Digital saviness
- Leadership skills
- Decision Making skills
Tasks
- Certify and release secondary packed drug product batches for commercial purposes
- Ensure compliance with AMG, Marketing Authorization, and GMP requirements
- Verify product quality and documentation for batch release
- Lead critical negotiations with internal and external stakeholders
- Provide coaching, performance management, and capability building
- Manage technical operations and provide day-to-day quality support
- Collaborate across functions to align on priorities, risks, and delivery commitments
- Participate in escalations, recalls, and critical complaint investigations
- Evaluate process changes and deviations
- Plan and deliver projects to agreed quality, scope, and timelines
- Ensure inspection and audit readiness
- Coordinate responses and drive timely, sustainable CAPAs
- Support preparation for and participation in audits and inspections
- Maintain and improve Quality Management System processes
- Oversee release management activities
- Report technical complaints, adverse events, and special case scenarios within 24 hours
- Coordinate distribution of marketing samples as needed
Work Experience
- approx. 4 - 6 years
Education
- Bachelor's degreeOR
- Master's degree
Languages
- English – Native
Tools & Technologies
- cGMP
- GxP
- QMS
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
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
QA Specialist Operations(m/w/x)
Full-time/Part-timeWith HomeofficeExperiencedKundlfrom 58,199.96 / year - Novartis
QA Compliance Expert(m/w/x)
Full-timeWith HomeofficeExperiencedSchaftenaufrom 64,023.54 / year - Novartis Pharmaceutical Manufacturing GmbH
QA Specialist Operations(m/w/x)
Full-time/Part-timeWith HomeofficeExperiencedKundlfrom 59,781.96 / year