Quality Inspector 1
Job description
The successful candidate for the position of Quality Inspector will possess the ability to support the activities listed below and be able to provide insights on how your past experiences contributed to connectivity with this role. This position is critical to the successful operation of the Devens Manufacturing Facility in that it contributes to a quality first culture in our pursuit toward a world-class operation.
What you’ll be doing Ensure all product inspections and product releases are completed in accordance with approved inspection criteria and procedures. Comply with all company policies and procedures, including Environmental, Health, and Safety (EHS) requirements. Perform incoming, in-process, and final product inspections, and document inspection results as required to assess product quality and conformance.
Maintain and verify the accuracy and completeness of quality records and documentation related to incoming material inspections, in-process inspections, and final product release. Collaborate cross-functionally with supervisors, managers, and production personnel to ensure quality standards are maintained and quality products are produced.
Maintain documentation in accordance with Good Documentation Practices (GDP). Ensure compliance with the Watson-Marlow Quality Management System (QMS). Use measuring and test equipment accurately and maintain equipment in accordance with established procedures. Maintain inspection and quarantine areas in an organized and compliant condition.
Review and verify packaging and labeling requirements to ensure compliance with applicable specifications and regulatory requirements. Assist in the investigation and resolution of nonconforming materials, including support for root cause analysis and corrective and preventive actions (CAPA). Support Environmental, Health, and Safety (EHS) initiatives, internal audits, and training activities as required.
Collect, analyze, and maintain quality data to support the monitoring and effectiveness of the Quality Management System. Provide support and backup coverage for Quality team members as needed. Participate in continuous improvement activities to enhance product quality, compliance, and operational efficiency. Perform other duties and responsibilities as assigned.
This is what you’ll need to be successful in this role Must have a strong commitment to site excellence. Passion for continuous improvement and desire to learn. Excellent attention to detail Knowledge of basic math and computer skills Performing inspections to assess product quality. Strong interpersonal and communication skills.
Ability to read and understand blueprints, drawings, specifications. Strong organizational skills Familiarity with ISO standards and its application in the Biopharmaceutical Manufacturing environment is a plus Ability to properly use test and measurement equipment (i.e., calipers, micrometers, height gages, etc.) Ability to stand for long periods of time.
Ability to lift 30 pounds. Work overtime as required. Ability to work within Clean Room as needed
Description copied from Flexicon A/S's careers page. Read the full posting before you apply.
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