About the role
Overview OSI Systems companies have a long history of developing innovative solutions to bring a better quality of life to the world. Our OSI Electronics (OSIE) division is a diversified manufacturer of electronic devices and value-added manufacturing services.
We provide our customers with the manufacturing capabilities and purchasing power of a global Electronics Manufacturing Services provider. By delivering regional and personalized support best provided by a smaller company, we strive to build lasting relationships and create close and valued partnerships with our customers. Our singular focus is to help security experts, clinical professionals and high-tech developers solve real-world problems and issues.
PFC Flexible Circuits, a division of OSI Electronics, has an oppourtunity for a highly motivated and detail oriented Validation Engineering CO-OP college student pursuing a diploma/degree in Biomedical, Chemical, Electrical or Mechanical Engineering. The selected candidate will have a solid academic background, effective communication and interpersonal skills, and be able to work in a fast-paced and dynamic industry.
- Onsite Work Hours: Mon to Fri: 8:30am to 5:00pm***
Responsibilities This CO-OP offers a unique opportunity to gain hands-on experience in a regulated manufacturing environment that produces products for the medical device industry. The individual will be responsible for assisting with the validation and qualification of manufacturing and testing equipment to ensure compliance with our internal quality systems and external regulatory standards, including ISO 13485.
- Support the generation and maintenance of validation documentation, including protocols, reports, and standard operating procedures (SOPs). Ensure all documentation is accurate, complete, and in compliance with company and regulatory requirements.
- Assist in the execution of validation protocols (Installation Qualification - IQ, Operational Qualification - OQ, and Performance Qualification - PQ) for new and existing manufacturing and laboratory equipment.
- Collect, analyze, and interpret data from validation studies. Present findings to the validation team and identify any discrepancies or issues.
- Assist with the coordination of equipment maintenance and calibration activities to ensure equipment remains in a qualified state.
- Learn and apply the principles of ISO 13485 and Good Manufacturing Practices (GMP). Participate in cross-functional teams to address quality-related issues and ensure continuous improvement.
- Assist in root cause analysis for any non-conformances identified during the validation process.
- Work closely with the Quality Assurance, Engineering, and Production teams to support validation activities and projects.
- Uphold the company’s core values of Integrity, Innovation, Accountability, and Teamwork.Demonstrate behavior consistent with the company’s Code of Ethics and Conduct.
- It is the responsibility of every employee to report to their manager or a member of senior management any quality problems or defects in order for corrective action to be implemented and to avoid recurrence of the problem.
- Duties may be modified or assigned at any time to meet the needs of the business.
Qualifications
- Must be enrolled in college during the 2025/2026 academic school year and be in good standing.
- Must be registered in the college co-op program (if selected, you will be required to provide proof of registration during the interview).
- A major in Biomedical, Chemical, Electrical, or Mechanical Engineering or related scientific discipline.
- Must have effective communication and interpersonal skills.
- Must have proactive attitude and a strong desire to learn and contribute.
OSI Systems, Inc. has three operating divisions: (a) Security, providing security and inspection systems, turnkey security screening solutions and related services; (b) Healthcare, providing patient monitoring, diagnostic cardiology and anesthesia systems; and (c) Optoelectronics and Manufacturing, providing specialized electronic components and electronic manufacturing services for original equipment manufacturers with applications in the defense, aerospace, medical and industrial markets, among others.
About OSI Electronics
OSI Electronics is a global Manufacturing Solutions provider headquartered in Hawthorne, CA, and Singapore. We are a division of OSI Systems, a publicly held corporation with annual sales exceeding $1.3 billion. Our production sites in the US, Canada, Mexico, England, Malaysia, Indonesia, and India provide our customers with a range of options to meet the specific needs of their markets.
Whether designing and building pre-production quantities or transitioning mature products to our low-cost region sites, OSI Electronics has the answer. With our certifications and experience supporting customers in the Medical, Industrial, Automotive, Communications, and Mil/Aero markets, we have the breadth of capabilities to meet the most stringent requirements.
Each of our EMS factories have ISO 9001, ISO 13485, and ISO 14001 certifications, to ensure compliance with commercial industrial, and medical customers as well as environmental safeguards. Selected sites are certificated to IATF 16949 and AS9100 to support their customers in the automotive and aerospace markets. Our Hawthorne facility is NADCAP accredited and handles ITAR and Secret projects.
To learn more about our capabilities, please visit our website at: www.osielectronics.com
About the role
Overview OSI Systems companies have a long history of developing innovative solutions to bring a better quality of life to the world. Our OSI Electronics (OSIE) division is a diversified manufacturer of electronic devices and value-added manufacturing services.
We provide our customers with the manufacturing capabilities and purchasing power of a global Electronics Manufacturing Services provider. By delivering regional and personalized support best provided by a smaller company, we strive to build lasting relationships and create close and valued partnerships with our customers. Our singular focus is to help security experts, clinical professionals and high-tech developers solve real-world problems and issues.
PFC Flexible Circuits, a division of OSI Electronics, has an oppourtunity for a highly motivated and detail oriented Validation Engineering CO-OP college student pursuing a diploma/degree in Biomedical, Chemical, Electrical or Mechanical Engineering. The selected candidate will have a solid academic background, effective communication and interpersonal skills, and be able to work in a fast-paced and dynamic industry.
- Onsite Work Hours: Mon to Fri: 8:30am to 5:00pm***
Responsibilities This CO-OP offers a unique opportunity to gain hands-on experience in a regulated manufacturing environment that produces products for the medical device industry. The individual will be responsible for assisting with the validation and qualification of manufacturing and testing equipment to ensure compliance with our internal quality systems and external regulatory standards, including ISO 13485.
- Support the generation and maintenance of validation documentation, including protocols, reports, and standard operating procedures (SOPs). Ensure all documentation is accurate, complete, and in compliance with company and regulatory requirements.
- Assist in the execution of validation protocols (Installation Qualification - IQ, Operational Qualification - OQ, and Performance Qualification - PQ) for new and existing manufacturing and laboratory equipment.
- Collect, analyze, and interpret data from validation studies. Present findings to the validation team and identify any discrepancies or issues.
- Assist with the coordination of equipment maintenance and calibration activities to ensure equipment remains in a qualified state.
- Learn and apply the principles of ISO 13485 and Good Manufacturing Practices (GMP). Participate in cross-functional teams to address quality-related issues and ensure continuous improvement.
- Assist in root cause analysis for any non-conformances identified during the validation process.
- Work closely with the Quality Assurance, Engineering, and Production teams to support validation activities and projects.
- Uphold the company’s core values of Integrity, Innovation, Accountability, and Teamwork.Demonstrate behavior consistent with the company’s Code of Ethics and Conduct.
- It is the responsibility of every employee to report to their manager or a member of senior management any quality problems or defects in order for corrective action to be implemented and to avoid recurrence of the problem.
- Duties may be modified or assigned at any time to meet the needs of the business.
Qualifications
- Must be enrolled in college during the 2025/2026 academic school year and be in good standing.
- Must be registered in the college co-op program (if selected, you will be required to provide proof of registration during the interview).
- A major in Biomedical, Chemical, Electrical, or Mechanical Engineering or related scientific discipline.
- Must have effective communication and interpersonal skills.
- Must have proactive attitude and a strong desire to learn and contribute.
OSI Systems, Inc. has three operating divisions: (a) Security, providing security and inspection systems, turnkey security screening solutions and related services; (b) Healthcare, providing patient monitoring, diagnostic cardiology and anesthesia systems; and (c) Optoelectronics and Manufacturing, providing specialized electronic components and electronic manufacturing services for original equipment manufacturers with applications in the defense, aerospace, medical and industrial markets, among others.
About OSI Electronics
OSI Electronics is a global Manufacturing Solutions provider headquartered in Hawthorne, CA, and Singapore. We are a division of OSI Systems, a publicly held corporation with annual sales exceeding $1.3 billion. Our production sites in the US, Canada, Mexico, England, Malaysia, Indonesia, and India provide our customers with a range of options to meet the specific needs of their markets.
Whether designing and building pre-production quantities or transitioning mature products to our low-cost region sites, OSI Electronics has the answer. With our certifications and experience supporting customers in the Medical, Industrial, Automotive, Communications, and Mil/Aero markets, we have the breadth of capabilities to meet the most stringent requirements.
Each of our EMS factories have ISO 9001, ISO 13485, and ISO 14001 certifications, to ensure compliance with commercial industrial, and medical customers as well as environmental safeguards. Selected sites are certificated to IATF 16949 and AS9100 to support their customers in the automotive and aerospace markets. Our Hawthorne facility is NADCAP accredited and handles ITAR and Secret projects.
To learn more about our capabilities, please visit our website at: www.osielectronics.com