Technician I, Process Development

Quasar Medical; California; On-site; USD 45,000 - 65,000; Full time

Job summary

Quasar Medical in California seeks a Technician I in Process Development to support developing, monitoring and optimizing critical process parameters for medical device manufacturing. The role collaborates with process engineering, conducts characterization studies, and assists with startup of new equipment.

Requires a high school diploma; relevant experience in medical devices preferred. Strong communication, organization and problem-solving skills.

Qualifications

• High school diploma required.

Responsibilities

• Develop and optimize processes for manufacturing medical devices.
• Conduct characterization studies.
• Process and manufacture medical devices.
• Assist with startup of new equipment.
• Troubleshoot issues related to process, machine and materials.
• Adhere to safety protocols to ensure a safe work environment.
• Follow Good Manufacturing Practices (GMPs).

Education

High school diploma

Job description

Technician I, Process Development### Technician I, Process DevelopmentApply: QUS California: Full time: Posted Yesterday**Our Culture** We strive for an inclusive company culture, where everyone feels valued, has a voice and is treated fairly, for their personal benefit, the benefit of Quasar, and the benefit of our customers and doctors using our products for patients in need. **Job Purpose:**The Process Technician is responsible for developing, monitoring, and optimizing critical process parameters used in the manufacturing of medical devices.**Duties and Responsibilities**Responsibilities include but not limited to:* In collaboration with process engineering team:* Develop and optimize processes for manufacturing medical devices.* Conduct characterization studies.* Process and manufacture medical devices.* Assist with the startup of new equipment.* Troubleshoot issues related to process, machine and materials.* Adhere to safety protocols to ensure a safe work environment.* Follow Good Manufacturing Practices (GMPs).**Education and Experience:*** High school diploma required.* Experience with medical devices or in similar regulated industry is a plus.* Good written and verbal communication skills.* Effective organizational & time management skills and attention to detail.* Strong problem-solving skills focused on root cause analysis.**Work Requirements*** Not all inclusive. Employee may perform other duties as assigned.* Reporting structures may change to meet the ongoing needs of the organization.* Travel: 10-20%**Working Conditions*** The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this position.* The employee will work in laboratories, on manufacturing lines, and in offices.* While performing the duties of this position, the employee is regularly required to talk or hear. The employee frequently is required to use hands or fingers, handle or feel objects. The employee is regularly required to stand, walk, sit, use hands and fingers, handle or feel and reach with hands and arms.* The employee will be exposed to and handle chemicals, and hazardous materials.* Specific vision abilities required by this position include close vision, distance vision, and the ability to adjust focus.* The employee must occasionally lift and/or move office products and supplies, up to 45 pounds.* The noise level in the work environment is usually low to moderate. **Join Our Global Team**Are you passionate about helping others? Our employees are dedicated to serving medical device customers who deliver life-giving therapies around the world. We seek individuals who are enthusiastic, intelligent and thrive in teamwork, with a strong aspiration to pursue a fulfilling and impactful career. At Quasar, every day is a new opportunity to make a difference.