Quality Engineer for Projects
Ver: 195
Dia de atualização: 17-04-2024
Localização: Le Locle Neuchâtel NE
Categoria: IT - Hardware / Rede Tecnologia da Informação Consultoria / Atendimento ao Cliente Artes / Design Legal / Contratos
Indústria:
Tipo de empregos: 100%, Temps de travail : 90-100%
Conteúdo do emprego
Responsible for design and evaluation of Quality Systems sampling plans and inspection methods.
Responsible for reviewing and recommending solutions to quality problems.
ESSENTIAL DUTIES AND RESPONSIBILITIES
Policies:
- Know and follow EES policies and procedures and ensure that direct reports know and follow EES policies and procedures related to work activities performed in area of responsibility.
- Evaluate and/or design sampling plans and process control plans for lot acceptance and control processes.
- Study the effectiveness of inspection activities.
- Design means for measuring accuracy and documenting of inspection work.
- Evaluate and recommend inspection gauges and test equipment. Investigate causes of sporadic defects.
- Provide consultation services to Quality Systems and Manufacturing departments.
- Hire, supervise and train QS technicians, as applicable.
- Implement process control systems.
- Provide technical support for component, product and process validations.
- Provide technical support for new product transfer.
- Coordinate training of manufacturing associates as applicable.
- Establish and maintain appropriate documentation as required for Quality Systems activities.
- Other responsibilities may be assigned and not all responsibilities listed may be assigned.
- Investigate identified quality problems.
- Develop systems for new processes as required.
- Support CAPA investigations and tasks, to determine root cause and corrective actions needed.
- Maintain trend information on field failures.
- Support manufacturing in analyzing manufacturing product lines to determine how or where within the manufacturing or inspection process, the root cause of non-conformances or customer complaints exist.
- Execute Statistical Analysis that includes: ANOVA, DOE, Weibull, GR&R, Capability, FMEA, KT and SPC as required.
- Perform, enhance and validations: for manufacturing processes, gauges, equipment, software and computerized systems as required.
- Prepare written protocols as necessary.
- Provide leadership and initiative to QS organization through continuous improvement projects.
- Interface with manufacturing area and other support groups to ensure department objectives are met.
- Follow all company safety policies and other safety precautions within the work area.
- Promote safety to all associates that enter the work area.
- Attend required safety training.
- Ensure that direct reports employ safe practices.
- Environmental: Participate in EMS management structure toward implementation and maintenance of EMS including continual improvement; pollution prevention; objectives and targets; and regulatory compliance. Participate and support the ISO 14001 Certification and Regulatory Audit process. Implement and follow all applicable EMS procedures. Adhere to the site’s EHS Code of Conduct.
- Job is directly responsible for managing other employees (e.g., hiring/termination and/or pay decisions, performance management).
- Report to Quality Systems Manager.
JOB QUALIFICATIONS
KNOWLEDGE REQUIREMENTS
- Excellent written and oral skills and the ability to organize and follow up on multiple priorities.
- Able to make solid decisions that will effectively support the business and company policies.
- Able to work in a self-paced environment and provide leadership to team as appropriate
- Team player.
- Project Management
- Able to understand application of regulatory requirements to the business.
- Able to analyze and develop quality methods. Responsible for writing clear and concise protocols, study reports, and procedures.
- This position requires consistent involvement with and knowledge of changes in regulations and standards.
- Aptitude to respond to shifting priorities through appropriate realignment of required tasks.
- Personal computers Proficiency required.
- Skilled in use of PC based systems including, but not limited to: word processing, inventory management, quality system, non-conforming product systems and data base management
- Bachelor’s Degree in Engineering or applied science.
- Minimum of three years’ experience in quality control in the medical product industry preferred.
Jabil, including its subsidiaries, is an equal opportunity employer and considers qualified applicants for employment without regard to race, color, religion, national origin, sex, sexual orientation, gender identify, age, disability, genetic information, veteran status, or any other characteristic protected by law.
Data limite: 01-06-2024
Clique para aplicar para o candidato livre
Reportar emprego
EMPREGOS SEMELHANTES
-
⏰ 28-05-2024🌏 Genève, Genève GE
-
⏰ 28-05-2024🌏 Zürich, Zürich ZH
-
⏰ 28-05-2024🌏 Genève, Genève GE
-
⏰ 28-05-2024🌏 Zürich, Zürich ZH
-
⏰ 28-05-2024🌏 Muttenz, Basel-Landschaft BL
-
⏰ 28-05-2024🌏 Schlieren, Zürich ZH
-
⏰ 28-05-2024🌏 Sarnen, Obwalden OW
-
⏰ 28-05-2024🌏 Zürich, Zürich ZH
-
⏰ 28-05-2024🌏 Zürich, Zürich ZH
-
⏰ 28-05-2024🌏 Zürich, Zürich ZH