Are Jobs in La Chaux-de-Fonds, NE
Zuletzt aktualisiert: vor 2 Tagen
Gi Life Sciences is looking for its partner in the Canton of Neuchâtel a : .SENIOR ENGINEER (MANUFACTURING COMPLIANCE).The Senior Engineer (Manufacturing Compliance) authors, owns and leads updates o...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
For our client, a world leader in the design and manufacture of automatic machines for the processing and packaging of pharmaceutical, food, and automation products, we are looking for a skilled.As...Mehr anzeigenZuletzt aktualisiert: vor 2 Tagen
We are an early-stage, venture-backed start-up that has raised over $50M from top-tier investors in Europe and the United States.
We have developed and brought to market the world’s first continuous...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Working at Freudenberg : We will wow your world!.You will manage the manufacturing process.Your task? To ensure compliance with production standards, customer specifications and performance targets ...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
If you're passionate about web applications, performance, and design, read on!.In this role, you’ll lead front-end development using .
You’ll collaborate closely with designers and developers to del...Mehr anzeigenZuletzt aktualisiert: vor 27 Tagen%20AG)
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Supervisor, Quality Compliance
Integra Lifesciences Switzerland SASLe Locle, CH Management of the complaint technicians’ team : Organize necessary resources to support activities.Ensure that goals and objectives are set and followed for every team member in accordance with the ...Mehr anzeigenZuletzt aktualisiert: vor 22 Tagen
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Principal Engineer Technology Development
OK Job SANeuchâtel, CH Master degree in Science or Engineering.Minimum 5-8 years of experience in a similar position, ideally built upon some practical experience in lithography-etch-metrology areas.Good understanding of...Mehr anzeigenZuletzt aktualisiert: vor 13 Tagen
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Quality Manager (M / W)
Adecco Human Resources AGNeuchâtel, CH For one of our clients, an industrial company based in the Neuchâtel area, we are looking for a Quality Manager (M / W) : .
Develop, implement, and maintain quality management systems and processes.Ensu...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Senior Engineer (Manufacturing Compliance)
Gi Group SANeuchâtel, Neuenburg, SchweizQuick Apply
sales manager (f / m / x)
Robert HalfNeuchâtel, Neuchâtel Vacancy : sales manager (f / m / x) -.We are looking for a sales manager (f / m / x) to start immediately for our client, in the IT industry.
The position is a direct permanent position with our customer.The...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Automation Engineer PLC programmer (French speaking)
LIONSCOUT GROUPNeuchâtel, SwitzerlandQuick Apply
Perfume Sustainability Manager
BulgariNeuchâtel To strengthen our Environment and Regulatory Affairs team within the Perfume Division based in Neuchâtel, we are recruiting a.
Perfume Sustainability Manager.You are responsible for overseeing the o...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Freight Forwarder Sea Freight (m / f / x)
DSVLa Chaux-de-Fonds, NE, CH Division : CHE - DSV Air & Sea AG (Air & Sea).Freight forwarders in DSV are acting as pro-active interface between the customer and all relevant internal and external service providers.You are ready...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
Senior Data Engineer
AktiiaNeuchâtel, NE, CHVollzeit
Quick Apply
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Senior Project Manager Microengineering (Master’s degree), W / M
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Quality Control Associate Director H / F
LHHNeuchâtel LHH Recruitment Solutions is a specialized talent recruitment agency.We provide tailored services to help companies find the best candidates for their staffing needs.
With deep industry expertise an...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
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Lead Frontend Developer
We Are 5 ValuesNeuchatel,Switzerland95.000,00 CHF–100.000,00 CHF jährlich
Vollzeit
Quick Apply
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Validation engineer
Randstad (Schweiz) AGNeuchâtel, CH We are currently seeking a Validation engineer for one of our clients in Canton of Neuchatel.If you are looking to work in a dynamic and very friendly working environment then this is for you.This ...Mehr anzeigenZuletzt aktualisiert: vor 13 Tagen
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Sales Manager Industrial Materials & Refining (H / F / N)
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You understand clients' needs and offer tailor-made solut...Mehr anzeigenZuletzt aktualisiert: vor 15 Tagen
QARA MAnager
EPM ScientificNeuchâtel A market leader for non-invasive technology are looking for a QARA Manager to be based at their growing site in Neuchatel.
This is an opportunity to join an international fast-paced organisation.The...Mehr anzeigenZuletzt aktualisiert: vor über 30 Tagen
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Supervisor, Quality Compliance
Integra Lifesciences Switzerland SASLe Locle, CHVor 22 Tagen
StellenbeschreibungA minimum of a Bachelors Degree is required, preferable in quality assurance, Engineering, a Life Science or a related technical discipline. Minimum of 5 years of professional work experience within a quality assurance or compliance audit environment is required. Experience in a Medical Device manufacturing environment is preferred. Fluent in French and English Knowledge of Medical device standards and regulations such as ISO13485, 93 / 42 EEC MDD, EUMDR, 21 CFR part 820, Canadian, Japanese, Australian, Brazilian regulations, etc. Strong management skills Strong communication, organizational, negotiation and interpersonal skills Strong analytical problem solving skills. The ability to collaborate with all levels of management across multiple sites and functions Ability to interface with internal and external customers Use of Agile, Oracle, EtQ, Minitab, Trackwise Use of Microsoft office tools Knowledge of statistical techniques Management of the complaint technicians’ team : Organize necessary resources to support activities. Ensure that goals and objectives are set and followed for every team member in accordance with the company’s G&O’s. Ensure polyvalence of the team Review and close complaint investigations for Le Locle Implementation and management of complaints procedures, investigation, trending, and product surveillance Ensures that Quality indicators (ex. Complaint, trends, etc.) are established and communicated Manage Health Hazard Evaluation when necessary : prepare the documentation and coordinate with others teams members (Design Quality Assurance, Medical Safety, Product Development, Post market Surveillance) to complete the required documentation Perform complaint trend analysis according to Integra GSOP : complete an investigation when necessary Participate to Post Market Surveillance activities : provide data Participate to risk analysis activities according to procedures and within the defined timeline Participate and support internal audits and third party audits / inspections Ensure that adequate Quality support is provided to production and to open projects / initiatives Ensure that Nonconformances are initiated, dispositioned, approved and investigated according to plans and in compliance with procedures and regulatory requirements Ensures that GMP rules are known, understood and respected on the site Escalates quality issues and makes sure that appropriate actions are in place to fix the issue in a compliant manner A minimum of a Bachelors Degree is required, preferable in quality assurance, Engineering, a Life Science or a related technical discipline. Minimum of 5 years of professional work experience within a quality assurance or compliance audit environment is required. Experience in a Medical Device manufacturing environment is preferred. Fluent in French and English Knowledge of Medical device standards and regulations such as ISO13485, 93 / 42 EEC MDD, EUMDR, 21 CFR part 820, Canadian, Japanese, Australian, Brazilian regulations, etc.
Responsabilities
- Management of the complaint technicians’ team : Organize necessary resources to support activities. Ensure that goals and objectives are set and followed for every team member in accordance with the company’s G&O’s.
- Ensure polyvalence of the team
- Review and close complaint investigations for Le Locle
- Implementation and management of complaints procedures, investigation, trending, and product surveillance
- Ensures that Quality indicators (ex. Complaint, trends, etc.) are established and communicated
- Manage Health Hazard Evaluation when necessary : prepare the documentation and coordinate with others teams members (Design Quality Assurance, Medical Safety, Product Development, Post market Surveillance) to complete the required documentation
- Perform complaint trend analysis according to Integra GSOP : complete an investigation when necessary
- Participate to Post Market Surveillance activities : provide data
- Participate to risk analysis activities according to procedures and within the defined timeline
- Participate and support internal audits and third party audits / inspections
- Ensure that adequate Quality support is provided to production and to open projects / initiatives
- Ensure that Nonconformances are initiated, dispositioned, approved and investigated according to plans and in compliance with procedures and regulatory requirements
- Ensures that GMP rules are known, understood and respected on the site
- Escalates quality issues and makes sure that appropriate actions are in place to fix the issue in a compliant manner
Qualifications
Job Description
Responsabilities
Qualifications