Real Staffing
What You'll Be Responsible For:
Leading and maintaining our ISO 13485-compliant QMS
Managing internal/external audits and reporting to the Executive Team
Supervising First Article, In-Process, and Final Inspections
Overseeing supplier quality and resolving non-conformances
Driving CAPA and root cause investigations
Handling customer complaints and quality communications
Building and developing a high-performing quality team
Managing clean room protocols, equipment qualifications, and process validations
Defining quality strategies and KPIs
Leading safety and IIPP compliance
Developing SOPs and delivering employee training
Required:
Bachelor's degree in manufacturing, engineering, medical device, or related field
4+ years in a Quality leadership role in manufacturing
3+ years managing ISO 13485 QMS and audits
Experience in precision component and contract manufacturing
Strong CAPA and root cause analysis skills
Proficiency in engineering drawings and inspection tools
Excellent communication and team leadership skills
Full-time, on-site availability in San Carlos, CA
EOE Statement: Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
In addition to base pay, direct-hire employees may be eligible for client offered benefits such as medical, dental, and vision coverage, and paid leave where required by applicable law. Eligibility may vary based on factors such as location and hire date and is subject to change.
To find out more about Real, please visit www.realstaffing.com
#J-18808-Ljbffr
Leading and maintaining our ISO 13485-compliant QMS
Managing internal/external audits and reporting to the Executive Team
Supervising First Article, In-Process, and Final Inspections
Overseeing supplier quality and resolving non-conformances
Driving CAPA and root cause investigations
Handling customer complaints and quality communications
Building and developing a high-performing quality team
Managing clean room protocols, equipment qualifications, and process validations
Defining quality strategies and KPIs
Leading safety and IIPP compliance
Developing SOPs and delivering employee training
Required:
Bachelor's degree in manufacturing, engineering, medical device, or related field
4+ years in a Quality leadership role in manufacturing
3+ years managing ISO 13485 QMS and audits
Experience in precision component and contract manufacturing
Strong CAPA and root cause analysis skills
Proficiency in engineering drawings and inspection tools
Excellent communication and team leadership skills
Full-time, on-site availability in San Carlos, CA
EOE Statement: Specialist Staffing Group is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.
In addition to base pay, direct-hire employees may be eligible for client offered benefits such as medical, dental, and vision coverage, and paid leave where required by applicable law. Eligibility may vary based on factors such as location and hire date and is subject to change.
To find out more about Real, please visit www.realstaffing.com
#J-18808-Ljbffr