WE
West Pharmaceutical Services23 Tage
Quality Control Manager(m/w/x)
Vollzeit
Senior
Keine Angabe
Stolberg
Nejo KI-Zusammenfassung
As a Quality Control Manager, you will oversee daily inspections and lead a dedicated team to ensure compliance with quality standards. This role involves improving processes, managing documentation, and fostering a culture of quality throughout manufacturing operations.
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Anforderungen
- •Associate's Degree in Technical or Engineering
- •Bachelor's Degree in Technical or Engineering
- •Minimum 8 years previous experience in Quality Control
- •Experience in FDA regulated environment, pertinent to ISO 15378
- •Familiarity with computers and various software programs
- •Compliance with company’s safety policy
- •Compliance with company’s quality policy
- •Support and contribute to Lean Sigma programs
- •Metrology Equipment experience
- •Leadership experience in leading teams
- •Decision making based on data analysis
- •Ability to generate, express, and exchange new ideas
- •Understanding direction and adherence to established procedures
- •Effective communication skills, both written and oral
- •Organizational skills for planning and prioritization
- •Ability to read and interpret data, information, and documents
- •Ability to work well with others in various situations
- •Ability to multi-task and work under time constraints
- •Ability to make independent and sound judgments
- •Adaptability to changes in the work environment
Abgeschlossene Berufsausbildung
ODER
Bachelor-Abschluss
Berufserfahrung
8 Jahre
Deine Aufgaben
- •Monitor daily quality inspections of incoming materials
- •Oversee in-process inspections and batch record reviews
- •Manage the Quality Control team to ensure timely inspections
- •Supervise quality control supervisors and resolve personnel issues
- •Conduct performance evaluations and manage disciplinary actions
- •Lead Incoming Inspection, In-Process Inspection, and Batch Release teams
- •Promote a 'quality at the source' mentality in manufacturing processes
- •Instill an 'immediate audit readiness' mindset in the team
- •Ensure compliance with quality system documents and regulations
- •Schedule and prioritize quality inspections and testing
- •Identify opportunities to improve processes and procedures
- •Support quality assurance activities by evaluating products and processes
- •Collaborate with technical staff on root cause analysis
- •Manage communications and visual checks to meet quality requirements
- •Review documentation for accuracy and determine product release status
- •Develop documentation and procedures for new equipment qualification
- •Create and improve Quality Control KPIs metrics
- •Set goals and objectives for the Quality Control organization
- •Support investigations related to non-conformances and audits
- •Ensure equipment maintenance and calibration are up to date
- •Maintain an organized QC area with a 5S mindset
- •Participate in special project teams as assigned
- •Perform other duties as assigned based on business needs
- •Comply with all laws, regulations, and safety rules
Tools & Technologien
Microsoft WordMicrosoft ExcelMaster-controlSAP
Sprachen
Englisch – verhandlungssicher
Deine Vorteile
Gesundheits- & Fitnessangebote
- •Physical health support
Mentale Gesundheitsförderung
- •Mental health support
- •Emotional health support
Sonstige Vorteile
- •Financial health support
Die Originalanzeige dieses Stellenangebotes in der aktuellsten Version findest du hier. Nejo hat diesen Job automatisch von der Website des Unternehmens West Pharmaceutical Services 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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