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NONovartis Pharma AG

Senior Quality Control Specialist(m/w/x)

Basel
ab CHF 85.400 - 158.600 / Jahr
Vollzeitmit HomeofficeSenior
Jetzt bewerben
Nejo KI-Zusammenfassung

Reviewing and approving analytical data for active substance manufacturing. Pharmaceutical industry experience with GxP standards required. Global recognition programs, flexible working options.

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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 within 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, and fluency in local language
  • Proficiency in MS Office and standard IT systems for Quality, laboratory, and documentation
  • Collaboration, result orientation, analytical problem-solving, resilience, operational excellence, continuous learning, and digital awareness

Aufgaben

  • Support the laboratory team with in-depth knowledge
  • Ensure efficient performance of laboratory activities and investigations
  • Ensure compliance with GxP and HSE guidelines
  • Review and approve analytical data
  • Plan, coordinate, and support sampling activities
  • Execute sampling activities
  • Document sampling activities
  • Align sampling with project and routine laboratory needs
  • Review, evaluate, and approve analytical test results
  • Approve analytical test results for release, stability, and project activities
  • Prepare analytical protocols, reports, and trend analyses
  • Review analytical protocols, reports, and trend analyses
  • Approve analytical protocols, reports, and trend analyses
  • Prepare, review, and approve KPIs/KQIs
  • Prepare, review, and approve registration-related documentation
  • Lead analytical project activities
  • Contribute to analytical project activities
  • Lead method implementation
  • Contribute to method implementation
  • Lead analytical transfers
  • Contribute to analytical transfers
  • Lead new product introduction
  • Contribute to new product introduction
  • Lead routine laboratory readiness
  • Contribute to routine laboratory readiness
  • Serve as Single Point of Contact for assigned products and activities
  • Serve as Subject Matter Expert for assigned products and activities
  • Manage deviations
  • Manage OOx investigations
  • Define CAPA
  • Manage analytical weak points
  • Manage continuous improvement actions
  • Ensure robust laboratory performance
  • Contribute to supplier qualification
  • Contribute to service provider management
  • Contribute to contract management
  • Contribute to SLA management
  • Contribute to SOW management
  • Contribute to QAA management
  • Contribute to budgeting activities
  • Contribute to cross-functional governance meetings
  • Ensure compliance with cGxP
  • Ensure compliance with data integrity requirements
  • Ensure compliance with Quality requirements
  • Ensure compliance with HSE requirements
  • Ensure equipment maintenance
  • Ensure calibration planning
  • Ensure training
  • Ensure risk identification
  • Ensure safe working practices

Ausbildung

Abgeschlossene BerufsausbildungODER
Bachelor-Abschluss

Sprachen

Englisch – fortgeschritten
local – fließend

Tools & Technologien

MS Office

Benefits

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
Boni & Prämien
  • Performance-based bonus
Attraktive Vergütung
  • Pay equity

Von Nejo automatisch aufbereitet

Nejo hat diesen Job automatisch von der Website des Unternehmens Novartis Pharma AG 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.

Zur Originalanzeige bei Novartis Pharma AG

Über das Unternehmen

NO
PharmaceuticalsBasel

The company is committed to integrating AI-powered tools into drug discovery to enhance data-driven solutions.

novartis.com
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