Product Quality Inspector

Job title:
Product Quality Inspector

Your role:

• 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.

Youre the right fit if: (4 x bullets max)
1. Experience- 4+yrs of Manufacturing Quality Experience prefer from Medtech industry
2. Skills- In-Process Outing going Quality, Final Quality, DEFOA, ISO 13485 prefer, 21 CFR 820, prefer, IPC A610 Certification prefer.
3. Education- Diploma in Electrical or Electronics
4. Anything else-

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  u2022 Digital Literacy
  u2022 Quality Specifications
  u2022 Quality Control Inspection
  u2022 Quality Management Systems (QMS)
  u2022 Troubleshooting
  u2022 Regulatory Requirements
  u2022 Technical Documentation
  u2022 Manufacturing Processes
  u2022 Process Improvements
  u2022 Quality Management Procedures and Methodologies
  u2022 Technical Acumen
  u2022 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 companyu2019s facilities.
Field roles are most effectively done outside of the companyu2019s main facilities, generally at the customersu2019 or suppliersu2019 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 wont 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.
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If youu2019re 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 .