Responsible for supporting diverse complex quality control tasks, assisting in resolving malfunctions, analyzing quality control improvements, working under limited supervision.
The role escalates issues as needed and contributes to planning activities, ensuring adherence to good laboratory practices (GLP) and good manufacturing practices (GMP).
The role helps in the documentation of regulatory requirements, supporting validation protocols, leading equipment maintenance, and adhering to safety protocols. The role escalates issues to superiors and participates in planning and priority settings within their area of responsibility.
Helps to execute diverse complex tasks based on individual understanding and technical knowledge to address abnormalities within operational manufacturing processes.
Assists in remedying complex malfunctions, helps to execute product quality inspection activities within the project scope.
Works with limited supervision, escalating issues to superiors as needed and develops a substantial understanding of relevant regulations, requirements, and standards.
Aids to implement quality control procedures and protocols, ensuring adherence to good laboratory practices (GLP) and good manufacturing practices (GMP).
Helps in the documentation of regulatory requirements for good manufacturing controls for medical devices as outlined in quality control plans, assisting in implementing the laboratory chemical hygiene program.
Provides support towards the execution of validation protocols and testing methods for new products and processes to ensure they meet quality standards.
Engages in continuous learning and on-the-job training to enhance skills and knowledge and ensures quality of own work by conducting checks and taking responsibility for the accuracy of work.
Adheres to all safety protocols and guidelines, including the proper handling and disposal of hazardous materials, to maintain a safe working environment for oneself and others.
Escalates issues to superiors and participates in planning and priority settings within their area of responsibility.
You're the right fit if: (4 x bullets max)
Experience- 4+yrs of Manufacturing Quality Experience prefer from Medtech industry
Skills- In-Process Outing going Quality, Final Quality, DEFOA, ISO 13485 prefer, 21 CFR 820, prefer, IPC A610 Certification prefer.
Education- Diploma in Electrical or Electronics
Anything else-
Digital Literacy
Quality Specifications
Quality Control Inspection
Quality Management Systems (QMS)
Troubleshooting
Regulatory Requirements
Technical Documentation
Manufacturing Processes
Process Improvements
Quality Management Procedures and Methodologies
Technical Acumen
Root Cause Analysis (RCA)
How We Work Together
We believe that we are better together than apart. For our office-based teams, this means working in-person at least 3 days per week.
Onsite roles require full-time presence in the company’s facilities.
Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations.
Indicate if this role is an office/field/onsite role.
About Philips
We are a health technology company. We built our entire company around the belief that every human matters, and we won't stop until everybody everywhere has access to the quality healthcare that we all deserve. Do the work of your life to help the lives of others.
Learn more about our business.
Discover our rich and exciting history.
Learn more about our purpose.
If you’re interested in this role and have many, but not all, of the experiences needed, we encourage you to apply. You may still be the right candidate for this or other opportunities at Philips. Learn more about our culture of impact with care here.
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