20 beste Stellen als production in la chaux de fonds, ne – aktuell auf Personalsuche

Associate Quality Assurance
Integra LifeSciences —Le Locle, NE
- 100%
- Management-Erfahrung
- Englisch
- Personalführung
Senior Director, Quality Operations EU
Integra LifeSciences —Le Locle, NE
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- Englisch
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International Creative Content Project Leader
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Maintenance Process Technician
Takeda Pharmaceutical —Neuenburg, NE
- CHF 67’100 - CHF 92’180 pro Jahr
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- 100%
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Apprentissage Horloger/ère de production CFC (3 ans) Villeret 2027
ETA SA Manufacture Horlogère Suisse —Villeret, BE
- 100%
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Compagnie des Montres Longines, Francillon S.A. —Saint-Imier, BE
- 100%
9 Tage
Low-Power Wireless SoC Architect
EM Microelectronic-Marin Ltd —Marin, NE
- 100%
- Doktorat
- Systemdesign
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Quality Engineer III
Jabil Circuit —Le Locle, NE
- 100%
- Englisch
- Analysefähigkeit
- Bachelor
Director, Human Resources Business Partner, Switzerland
Bristol-Myers Squibb —Boudry, NE
- 100%
- Microsoft Excel
- Management-Erfahrung
- Bachelor
8 Tage
Gestionnaire production ferroviaire
TransN —La Chaux-de-Fonds, NE
- Teilzeit
Responsable Secteur de Production
Richemont —La Chaux-de-Fonds, NE
- 100%
- Management-Erfahrung
- Keine Ausbildung erforderlich
- Ohne Hochschulabschluss
12 Tage
International Therapeutic Area Head
Bristol-Myers Squibb —Boudry, NE
- 100%
- Microsoft Excel
- Doktorat
- Forschungserfahrung
12 Tage
CPSO Sr Manager Launch Excellence
Bristol-Myers Squibb —Boudry, NE
- 100%
- Microsoft Excel
- Projektmanagement
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International Therapeutic Area Head (iTAH)
Bristol-Myers Squibb —Boudry, NE
- 100%
- Microsoft Excel
- Doktorat
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12 Tage
Master Data Steward
Straumann Group —Villeret, BE
- 100%
- Microsoft Excel
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- SQL
Senior Specialist, Manufacturing Scheduling
Bristol-Myers Squibb —Boudry, NE
- 100%
- Microsoft Excel
- Oracle
- Management-Erfahrung
13 Tage
Installatrice ou installateur électricien·ne CFC, orientation installations photovoltaïque 80-100%
Groupe E SA —Boudry, NE
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Technicien de production / Régleur
Mat-Cut SA —La Chaux-de-Fonds, NE
- CHF 4’000 - CHF 5’000 pro Monat
- 100%
- Wartung
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Direkt bewerben
8 Tage
Constructeur Habillage
Bulgari —Saignelégier, JU
- 100%
- Englisch
- Kostenloser Parkplatz
- Homeoffice-Möglichkeit

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Associate Quality Assurance

Integra LifeSciences -
Le Locle, NE

Jetzt bewerben

Details zur Stelle

100% | Pensum: 90-100%

Qualifikationen

Französisch
Management-Erfahrung
Mehrsprachig
Englisch
Personalführung
Qualitätssicherung
Bachelor
Kontinuierlicher Verbesserungsprozess
Risikomanagement
Produktion
Kommunikationsfähigkeit

Vollständige Stellenbeschreibung

Changing lives. Building Careers.

Joining us is a chance for you to do important work that creates change and shapes the future of healthcare. Thinking differently is what we do best. To us, change equals opportunity. Every day, more than 4,000 of us are challenging what’s possible and making headway to help improve outcomes.

The Associate Manager, Quality Assurance is responsible for overseeing quality systems and ensuring compliance with regulatory requirements and company standards. This role provides leadership for nonconformance investigations, production quality support, and sterility assurance activities to maintain product quality, patient safety, and operational excellence.

Key Responsibilities

Nonconformance Management

Supervise the identification, documentation, investigation, and closure of nonconformance events.
Ensure timely root cause analysis and implementation of corrective and preventive actions (CAPA).
Review and approve investigation reports to ensure compliance with GMP and internal procedures.
Monitor quality metrics and identify trends requiring escalation or improvement.

Production Quality Support

Provide Quality Assurance oversight and support to manufacturing operations.
Partner with Production, Engineering, Validation, and Supply Chain teams to resolve quality issues.
Review batch records, deviations, and change controls to ensure product disposition decisions are made appropriately.
Support process improvements while maintaining regulatory compliance.

Sterility Assurance

Oversee sterility assurance programs for aseptic manufacturing processes.
Ensure compliance with cGMP, FDA, EMA, and other applicable regulatory requirements.
Review environmental monitoring data, media fills, and contamination control strategies.
Collaborate with microbiology and manufacturing teams to investigate sterility-related events and implement corrective actions.

Leadership and Compliance

Supervise and mentor QA personnel to ensure effective performance and professional development.
Support internal audits, regulatory inspections, and customer audits.
Promote a culture of quality and continuous improvement.
Ensure adherence to quality policies, procedures, and documentation practices.

Qualifications

Bachelor's degree in Biology, Microbiology, Chemistry, Pharmaceutical Sciences, Engineering, or a related field.
5+ years of experience in Quality Assurance within pharmaceutical, biotechnology, or medical device manufacturing.
Experience with nonconformance investigations, CAPA, and GMP regulations.
Knowledge of aseptic processing and sterility assurance principles.
Strong leadership, problem-solving, and communication skills.
Familiarity with FDA, EMA, and international regulatory requirements.
Fluent in French and English

Preferred Qualifications

Previous supervisory or people-management experience.
Experience supporting aseptic or sterile manufacturing environments.
Knowledge of risk management tools and continuous improvement methodologies.

Unsolicited Agency Submission

Integra LifeSciences does not accept unsolicited assistance from search firms for employment opportunities. All CVs/resumes submitted by search firms to any employee at our company without a valid written search agreement in place for this position will be deemed the sole property of our company. No fee will be paid in the event a candidate is hired by our company as a result of an agency referral where no pre-existing agreement is in place. A formal written agreement is required before engaging any agency, and it must be executed and authorized by the Vice President, Talent Acquisition. Where agency agreements are in place, introductions (the initial sharing of a candidate’s name, resume, or background) are position-specific and may only occur within the scope of that approved agreement. Please, no phone calls or emails.

Jetzt bewerben

Erweiterte Suche

production Jobs in la chaux de fonds, ne

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Technicien de production / Régleur

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Ich möchte aktuelle Job-E-Mails für Stellen als production in la chaux de fonds, ne erhalten

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Weitere Job-Standorte erkunden

Key Responsibilities

Nonconformance Management

Production Quality Support

Sterility Assurance

Leadership and Compliance

Qualifications

Preferred Qualifications

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