Novartis Pharma AG
Analytical Project Lead(m/w/x)
Vollzeitmit HomeofficeSenior
Basel
ab CHF 126.000 - 234.000 / Jahr
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Reviewing and approving analytical data for bioanalytics in a GMP-regulated pharmaceutical environment. Strong knowledge of QC testing and GxP standards required. Performance-based bonus, global recognition programs.
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Anforderungen
- Technical education or university degree in Pharmacy, Chemistry, or related scientific discipline
- Experience in pharmaceutical industry, active substance manufacturing, or analytical laboratories in GMP-regulated environment
- Strong knowledge of Quality Control testing, sampling, laboratory equipment, GxP standards, data integrity, and quality decision-making
- Experience supporting analytical release, stability testing, method transfers, deviations, CAPAs, trend analysis, and project documentation
- Effective collaboration across functions, departments, external partners, and project teams
- Strong communication skills, good written and spoken English
- Proficiency in MS Office and standard IT systems
- Collaboration, result orientation, analytical problem-solving, resilience, operational excellence, continuous learning, and digital awareness
- Collaboration, Data Integrity, Decision Making, Leadership, Operational Excellence
Aufgaben
- Support laboratory team with bioanalytics knowledge
- Ensure compliance with GxP and HSE guidelines
- Review and approve analytical data
- Plan and coordinate sampling activities
- Support project and routine laboratory needs
- Review and approve analytical test results
- Prepare and approve analytical protocols
- Review and approve trend analyses
- Prepare and approve KPIs and KQIs
- Prepare and approve registration-related documentation
- Lead analytical project activities
- Contribute to method implementation
- Conduct analytical transfers
- Support new product introduction
- Ensure routine laboratory readiness
- Serve as Single Point of Contact for assigned products
- Act as Subject Matter Expert for pipeline activities
- Support external initiatives
- Prepare for audits and inspections
- Conduct technical assessments
- Manage deviations and OOx investigations
- Define and implement CAPA actions
- Address analytical weak points
- Drive continuous improvement actions
- Contribute to supplier qualification
- Manage service provider relationships
- Handle contracts, SLAs, SOWs, and QAAs
- Participate in budgeting activities
- Attend cross-functional governance meetings
- Ensure cGxP compliance
- Maintain data integrity
- Ensure quality standards
- Plan and manage equipment maintenance
- Schedule and oversee calibration
- Conduct training sessions
- Identify and mitigate risks
- Promote safe working practices
Ausbildung
Abgeschlossene BerufsausbildungODER
Bachelor-Abschluss
Sprachen
Englisch – verhandlungssicher
local – fließend
Tools & Technologien
MS Office
Benefits
Boni & Prämien
- Performance-based bonus
Sonstige Vorteile
- Insurance plans
- Global recognition programs
Betriebliche Altersvorsorge
- Retirement plans
Mentale Gesundheitsförderung
- Wellbeing resources
Flexibles Arbeiten
- Flexible working options
- Hybrid working options
Großzügige Elternzeit
- 14 weeks paid parental leave
Von Nejo automatisch aufbereitet
Nejo hat diesen Job automatisch von der Website des Unternehmens Novartis erfasst und die Informationen auf Nejo mit Hilfe von KI für dich aufbereitet. Trotz sorgfältiger Analyse können einzelne Informationen unvollständig oder ungenau sein. Bitte prüfe immer alle Angaben in der Originalanzeige! Inhalte und Urheberrechte der Originalanzeige liegen beim ausschreibenden Unternehmen.
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PharmaceuticalsBasel
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