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Performs a variety of tasks and conducts test procedures in regards to the quality process, ensuring that the pre-determined high standards of quality are achieved and maintained. Reports directly to the Senior Quality Engineer.
Requirements:
Ideally have a third level qualification in Quality/Mechanical/Plastic Engineering and/or have relevant industrial experience in a high volume injection-moulding environment.
Computer literacy required.
Must possess good communication/interpersonal skills; must be detail oriented, organized, flexible and be able to handle multiple tasks and time critical projects/deadlines.
Must understand the principles of Batch Control and FIFO.
Basic knowledge of statistical sampling of product
Must be able to hold a high degree of confidentiality.
Must have knowledge of EU-GMP
Understanding of injection moulding processes.
Working knowledge of ISO 9001/ ISO 13485 and FDA Code of Regulations CFR part 820 preferred.
Essential Duties and Responsibilities:
Review and approval of metrology reports, where appropriate, for batch release and validation purposes
New product validation, analysis and reporting.
Quality support to Engineering and Production Departments.
Establish and maintain documentation in line with West Dublin and West Pharmaceutical Services Quality Systems.
Liaise with customers and suppliers on new and existing projects.
Receiving and inspection of incoming goods and materials
Ensure that all parts/ materials, which require incoming inspection, conform to all requirements and applicable drawings and specifications.
Maintain good communications both internally and externally.
Ensures that all metrology equipment is correctly calibrated.
Assists shift personnel with quality issues and/or measurement techniques.
Assists in problem resolution with customers.
Makes periodic audits as requested and completes necessary documentation.
Archives quality records, samples and log procedures.
Makes periodic clean-out of records and samples exceeding minimum retention requirements as per West procedures.
Batch paperwork review and final decision to release product for shipment
Act in accordance with the company’s Guiding Principles and adherence to the corporate Code of Conduct.
Compliance to all site Environmental, Health and Safety requirements, training and regulations.
Compliance to all local site company policies, procedures and corporate policies.
Perform additional duties at the request of the direct supervisor.
Delegation of Duties:
When absent from the site duties and responsibilities will be delegated to the following designates
Job Title Quality Engineer
Job Title Senior Quality Engineer
Job Title Quality Engineering Manager
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