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You will be updated with latest job alerts via emailPosition Summary:
This role is responsible to ensure that design transfer and manufacturing operations activities are executed in compliance with Illuminas established Quality Management System (QMS) and relevant international/national regulations. These activities include but are not limited to validation non-conformance customer complaints risk assessment and support maintenance of the QMS.
Position Responsibilities:
Serve as Quality representative on project teams for new product transfers
Review and approve manufacturing operational activities such as Device History Records (DHR) nonconformance CAPA RMA and customer complaints
Work with cross-functional teams to resolve operational quality issues
Trend analyze and monitor key performance indicators suggest improvements and escalate to supervisor/management as necessary
Ensure the quality systems meet customer corporate or internal requirements and any other related requirement within the Quality Management System
Participate in management of corrective action program (customer complaints) to ensure timely follow-up completion and documentation of corrective actions
Manage customer complaints and work closely with cross function in issue investigation and ensure timely response of to corporate/ customer
Work in accordance with procedures and integrated program plans for achieving and maintaining the required level of product quality in preparation for FDA and ISO third party audits
Other such duties that may be determined by Supervisor
All listed tasks and responsibilities are deemed as essential functions to this position; however business conditions may require reasonable accommodations for additional task and responsibilities.
Position Requirements:
Bachelors degree in Engineering or Biological/Life Sciences or equivalent field
Minimum 5 years of experience in a medical device manufacturing environment.
Excellent interpersonal verbal and written communication skills
Ability to apply experience to meet 21 CFR 820 and ISO 13485 requirements
Strong analytical problem-solving and decision-making skills; Certified Quality Engineer or equivalent is a plus
Experience in failure investigation technical report writing data mining trend analysis and statistical analysis
Intermediate to advanced experience with words processing and spreadsheets charting graphing tools and presentation tools
Proficient in computer systems such as Microsoft Office & SAP
Experience with statistical analysis packages e.g. JMP Minitab is highly preferred
Required Experience:
Senior IC
Full-Time