Overview
Full Time
Skills
Inspection
Testing
Pharmaceuticals
Manufacturing
FMEA
Corrective And Preventive Action
PPAP
ISO 13485
Medical Devices
English
Communication
Process Flow
Mapping
Risk Assessment
Management
Legal
Job Details
Work Flexibility: Onsite
What you will do:
What you will need:
Required:
Desirable:
Travel Percentage: 20%
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.
Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.
What you will do:
- Support the design and testing of new products.
- Ensure that everything functions well and meets quality standards.
- Identify and prevent potential problems (especially risks, defects, and inspection issues).
- Ensure the product can be manufactured efficiently and safely.
- Support validations (process, tool, and equipment testing)
What you will need:
Required:
- University degree in engineering (or similar).
- Experience in regulated industries, such as medical devices or pharmaceuticals.
- Understanding of manufacturing processes and quality tools such as FMEA (Failure Mode and Effects Analysis), CAPA (Corrective and Preventive Actions), PPAP (Production Part Approval Process), validations, and inspections.
- Knowledge of standards such as ISO 13485 (quality standard for medical devices).
- Advanced English communication skills
Desirable:
- Experience with Process Flow Mapping (PFM) or process risk assessment.
- Experience with non-conformity management.
Travel Percentage: 20%
Stryker Corporation is an equal opportunity employer. Qualified applicants will receive consideration for employment without regard to race, ethnicity, color, religion, sex, gender identity, sexual orientation, national origin, disability, or protected veteran status. Stryker is an EO employer - M/F/Veteran/Disability.
Stryker Corporation will not discharge or in any other manner discriminate against employees or applicants because they have inquired about, discussed, or disclosed their own pay or the pay of another employee or applicant. However, employees who have access to the compensation information of other employees or applicants as a part of their essential job functions cannot disclose the pay of other employees or applicants to individuals who do not otherwise have access to compensation information, unless the disclosure is (a) in response to a formal complaint or charge, (b) in furtherance of an investigation, proceeding, hearing, or action, including an investigation conducted by the employer, or (c) consistent with the contractor's legal duty to furnish information.
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.