Quality Engineer
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Job Location:
Monthly Salary:
Posted on:
14 hours ago
Vacancies:
1 Vacancy
Job Summary
Job Title
Quality EngineerJob Description
Your role:
- Execute diverse and complex quality control tasks using technical knowledge to address abnormalities in manufacturing processes.
- Assist in resolving complex malfunctions and perform product quality inspection activities within project scope.
- Work independently on routine tasks while escalating issues to supervisors as needed.
- Aids to implement quality control procedures and protocols ensuring adherence to good laboratory practices (GLP) and good manufacturing practices (GMP).
- Support documentation of regulatory requirements for medicaldevice manufacturing controls and assist with the laboratory chemical hygiene program.
- Contribute to validation protocols testing methods and qualification activities for new products and processes.
- Maintain high accuracy by conducting selfchecks and taking ownership of the quality of your work.
- Follow all safety protocols including safe handling and disposal of hazardous materials to ensure a safe working environment.
- Participate in planning prioritization and continuous learning to strengthen quality and technical capability.
Youre the right fit if you have:
- Bachelors degree in Engineering Life Sciences or related technical field.
- Atleast 3 years relevant experience in manufacturing quality or QC within a regulated environment
- Solid understanding of GLP GMP and core regulatory expectations.
- Handson experience with SPC (Statistical Process Control) and datadriven process monitoring.
- Proficiency in Minitab for statistical analysis control charts capability studies and trend evaluation.
- Strong statistical analysis skills (e.g. hypothesis testing regression Pareto Cpk/Ppk).
- Working knowledge of CAPA processes including root cause analysis and corrective/preventive action implementation.
- Ability to create interpret and execute Quality Control Plans and Quality Plans aligned with manufacturing and regulatory requirements.
- Familiarity with structured problemsolving methodologies such as 8D 5 Why and fishbone analysis.
- Strong analytical thinking documentation discipline and attention to detail.
- Ability to work under limited supervision while communicating effectively and escalating issues when necessary.
- Commitment to safety compliance continuous improvement and maintaining high standards of quality work.
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 companys facilities.
Field roles are most effectively done outside of the companys main facilities generally at the customers or suppliers locations.
This is an 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.
Learn more about our business.
Discover our rich and exciting history.
Learn more about our purpose.
If youre 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.
Required Experience:
IC
Key Skills
- APQP
- Quality Assurance
- Six Sigma
- ISO 9001
- PPAP
- Minitab
- Root cause Analysis
- ISO 13485
- Quality Systems
- Quality Management
- As9100
- Manufacturing
About Company
Philips has been revolutionizing lighting for over 125 years. We pioneered the world changing development of electric light and LED, and are now leading the way in intelligent lighting systems. Our deep understanding of how lighting positively affects people, enables us to deliver inn ... View more
