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QC Finished Goods Supervisor(m/w/x)

12391 Haleon CH SARL
Nyon

Du leitest das QC-Team, sorgst für die Einhaltung von Sicherheits- und Qualitätsstandards und unterstützt Mitarbeiter bei Verbesserungsprojekten.

Anforderungen

  • •High School Diploma or equivalent
  • •Master’s Degree in Science or Engineering
  • •10 years relevant laboratory experience
  • •10 years in a leadership role
  • •Experience in FDA-regulated environment preferred
  • •Knowledge of GMP requirements preferred
  • •Project management experience preferred
  • •SAP knowledge preferred
  • •Computer knowledge: Excel, Word, PowerPoint
  • •Understanding of Root Cause Analysis
  • •Strong interpersonal and communication skills
  • •Coaching and problem-solving skills
  • •Ability to lead teams through change
  • •Drive continuous improvement
  • •Ability to work with minimal supervision
  • •Proactive traits

Deine Aufgaben

  • •EHS-Richtlinien kennen und einhalten
  • •Unsichere Bedingungen und Vorfälle melden
  • •Persönliche Schutzausrüstung tragen
  • •An EHS-Schulung teilnehmen
  • •Qualitätsstandards einhalten
  • •Sicherheits- und Qualitätsuntersuchungen durchführen
  • •Teamleitung im FMCG-Produktionsumfeld übernehmen
  • •Standards für Sicherheit, Qualität und Output festlegen
  • •Analytische Bewertungen genehmigen
  • •Daten für analytische Aktivitäten bereitstellen
  • •Problemlösungs- und Leistungsmanagement-Tools nutzen
  • •Echtzeit-Problemerkennung und kontinuierliche Verbesserung antreiben
  • •Leitender Untersucher für komplexe Lab-Untersuchungen sein
  • •Aktivitäten zur Fertigprodukt- und QC-Validierung planen
  • •Talente im Team identifizieren und entwickeln
  • •Aufgabenzuweisung und Personalaufstockung überwachen
  • •Verbesserungsprojekte coachen und unterstützen

Original Beschreibung

# QC Finished Goods Supervisor **Nyon Main Site** | **Full time** **Job purpose:** The purpose of the Supervisor role is to develop and lead a department to consistently deliver outstanding safety, quality, service, and value. The supervisor manages Team Leader, Scientist and Senior analysts of the department. This role is crucial in ensuring that the business strategy is executed through an engaged, motivated, and capable team. The role will ensure that our site maintains the highest standards in Environment, Health, Safety, and Wellness (EHSW) and Quality while achieving objectives of Nyon site. **Key Responsibilities:** **EHS Responsibilities– All Associates** * Know, understand, and comply with all Environment, Health, and Safety (EHS) guidelines. Report unsafe conditions, all injuries, illnesses, and hazardous materials releases. Wear personal protective equipment, attend EHS training programs, and follow all safe work procedures. **Quality Responsibilities– All Associates** * Adhere to all Quality Compliance standards (Data Integrity, Deviation, Lab Investigation, etc.) including QMS policy and regulatory requirements. **Job Responsibilities** * **Compliance:** Ensure compliance with EHS, cGMP, and Quality standards. Conduct safety and quality investigations as needed. Lead by example in adhering to company policies and procedures. SME during the audit * **People Leadership:** Full leadership of a team of scientist, Team Leader and senior analysts within a fast-moving consumer goods (FMCG) production environment, ensuring adherence to safety, quality, compliance, and output standards. * **Process Management:** Establish and confirm standards (4M’s: Material, Manpower, Method, Measurement) for managing safety, quality, and output. Primary contact of the PCT out. Approve Analytical Assessment (ICH Q3D, Q3C, sVMP…), Analytical protocols and reports. Ensure all analytical activities related to VMP and Pharmacopeia remediations are delivered on time. Provide data to anticipate analytical activities (SRM program) * **Performance Management:** Use tools for problem-solving and performance management. Drive real-time issue identification, resolution, and continuous improvement initiatives. Act as lead investigator for complex Lab Investigation/Deviation. Schedule all activities related to Finish product and QC Validation (QC Smart). Provide KPI. Support implementation of new projects (eg : New Software, robots….). Schedule all activities related to FG activities (QC Smart) in collaboration with Team Leader. * **Talent Development:** Identify and develop key talent within the team, ensuring regular development plans are executed. Set performance expectations and provide regular feedback. * **Resource Management:** Oversee task assignment, staffing, and recruitment efforts. * **Project Implementation:** Coach and support implementation improvement projects, managing scope, schedule, and cost. **Knowledge/ Education/ Experience Required** * High School Diploma or equivalent with 10 years of relevant experience in a Laboratory environment / Master’s Degree in Science, Engineering, or related field. * 10 years in a leadership role within a laboratory environment, in a regulated industry (e.g., pharmaceutical, FMCG). * Preferred: Experience in an FDA-regulated environment, GMP requirements, project management, SAP. * Computer knowledge (Excel, Word, Power Point). * Understanding of Root Cause Analysis. * Strong interpersonal, communication, coach and problem-solving skills. * Ability to lead teams through change and drive continuous improvement. * Ability to work in a fast-paced environment with minimal supervision. * Be proactive Haleon is an Equal Opportunity Employer. All qualified applicants will receive equal consideration for employment without regard to race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, covered/protected veteran status or any other federal, state or local protected class. Accommodation Requests If you require a reasonable accommodation or other assistance to apply for a job at Haleon at any stage of the application process, please let your recruiter know by providing them with a description of specific accommodations you are requesting. We’ll provide all reasonable accommodations to support you throughout the recruitment process and treat all information you provide us in confidence.
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