STAAR Surgical Jobs Hiring Now
STAAR Surgical is hiring for 12 open roles on Migrate Mate as of July 16, 2026, concentrated in business analysis and cloud engineering, with listed salaries up to about $270,000. Migrate Mate updates STAAR Surgical's live openings daily. STAAR Surgical is a medical device company focused on the development and manufacturing of implantable lenses and surgical equipment for vision correction procedures.
Find STAAR Surgical JobsOverview
STAAR Surgical hiring data on Migrate Mate, as of July 16, 2026.
- Open jobs
- 12
- Top team
- Business Analysis
- Seniority
- Mid to senior level
- Work type
- 0% remote or hybrid
- Top location
- Lake Forest
- Salary range
- $75,000–$270,000
Listed salaries for STAAR Surgical roles on Migrate Mate range from about $75,000 to $270,000 per year across 12 open roles, as of July 16, 2026. Some roles list hourly contract rates.
Open Roles at STAAR Surgical
Showing 12 of 12+ STAAR Surgical jobs
Group: NC and CAPA
MAIN JOB RESPONSIBILITIES / COMPETENCIES
1. Support site production, operations, and quality and R&D teams by addressing emergent issues that might arise due to the operation processes. Serve as the quality representative during any product or process investigation. Lead investigations including root cause analysis and health risk assessment of the identified product or process nonconformities.
2. Prepare and execute validations, technical studies, test method validations and other studies / reports as required. This includes preparation of protocols, establishment of test methodology and acceptance criteria, training personnel, execution, data analysis, investigation, and writing final reports.
3. Support project teams on non-conformance investigations regarding component failures, finished goods failures, and product returns. This includes but is not limited to performing risk analysis, determining root cause and recommending corrective action and SCRs.
4. Support internal audits and supplier audits. This includes preparation of audit plans, audit reports, and verifying SCRs have been completed.
5. Support project teams on Corrective Action/Preventive Action (CAPA) projects. This includes, but is not limited to, performing risk analysis, root cause analysis; developing a corrective action plan, implementing the plan, and submitting a summary report for project closure and conduct effectiveness checks (EC).
6. Assist Complaint Handling Department with technical/engineering support regarding customer complaints and product returns. Investigation may involve reviewing manufacturing batch records, vendor component records, MRB records, etc. to determine root cause of product failure.
7. Prepare and report appropriate metrics to Quality management.
8. Participate in Design Project Teams as a QA Representative to ensure that input requirements (internal, external, and customer) are clearly defined, risk assessment is performed, output meets input requirements, and objective evidence clearly supports conclusions. Additionally, ensure that quality related issues are adequately addressed. Perform quality related design control activities as assigned by Design Project Team. Partner with production during Design Transfer phase to ensure that products and processes meet all quality requirements.
9. Support internal team during audits at Monrovia sites; participate in the preparation and completion of corrective action plans as needed.
10. Other duties as assigned.
REQUIREMENTS
- Bachelor’s degree, preferably in science or engineering or equivalent combination of education/experience.
- Two years’ experience or advanced degree with one year of experience in quality engineering in the medical device or pharmaceutical industries is preferred.
- General knowledge of manufacturing processes such as injection molding, assembly, packaging, and sterilization is preferred.
- Solid understanding of investigation techniques including design of experiments and root cause analysis.
- Solid grasp of basic statistical techniques with basic understanding of advanced techniques in data analysis.
- Excellent project management, organization, writing and presentation skills required.
- Demonstrated expert knowledge of Windows-based software, including Word, Excel, Access, Project, and Power Point.
- Must be highly proficient in written and verbal communication.
Pay range: $75K-$95K Final compensation/salary will depend on experience
STAAR Surgical is an Equal Opportunity/Affirmative Action employer and all qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran or disability status, or any other characteristic protected by law. #USA
Group: NC and CAPA
MAIN JOB RESPONSIBILITIES / COMPETENCIES
1. Support site production, operations, and quality and R&D teams by addressing emergent issues that might arise due to the operation processes. Serve as the quality representative during any product or process investigation. Lead investigations including root cause analysis and health risk assessment of the identified product or process nonconformities.
2. Prepare and execute validations, technical studies, test method validations and other studies / reports as required. This includes preparation of protocols, establishment of test methodology and acceptance criteria, training personnel, execution, data analysis, investigation, and writing final reports.
3. Support project teams on non-conformance investigations regarding component failures, finished goods failures, and product returns. This includes but is not limited to performing risk analysis, determining root cause and recommending corrective action and SCRs.
4. Support internal audits and supplier audits. This includes preparation of audit plans, audit reports, and verifying SCRs have been completed.
5. Support project teams on Corrective Action/Preventive Action (CAPA) projects. This includes, but is not limited to, performing risk analysis, root cause analysis; developing a corrective action plan, implementing the plan, and submitting a summary report for project closure and conduct effectiveness checks (EC).
6. Assist Complaint Handling Department with technical/engineering support regarding customer complaints and product returns. Investigation may involve reviewing manufacturing batch records, vendor component records, MRB records, etc. to determine root cause of product failure.
7. Prepare and report appropriate metrics to Quality management.
8. Participate in Design Project Teams as a QA Representative to ensure that input requirements (internal, external, and customer) are clearly defined, risk assessment is performed, output meets input requirements, and objective evidence clearly supports conclusions. Additionally, ensure that quality related issues are adequately addressed. Perform quality related design control activities as assigned by Design Project Team. Partner with production during Design Transfer phase to ensure that products and processes meet all quality requirements.
9. Support internal team during audits at Monrovia sites; participate in the preparation and completion of corrective action plans as needed.
10. Other duties as assigned.
REQUIREMENTS
- Bachelor’s degree, preferably in science or engineering or equivalent combination of education/experience.
- Two years’ experience or advanced degree with one year of experience in quality engineering in the medical device or pharmaceutical industries is preferred.
- General knowledge of manufacturing processes such as injection molding, assembly, packaging, and sterilization is preferred.
- Solid understanding of investigation techniques including design of experiments and root cause analysis.
- Solid grasp of basic statistical techniques with basic understanding of advanced techniques in data analysis.
- Excellent project management, organization, writing and presentation skills required.
- Demonstrated expert knowledge of Windows-based software, including Word, Excel, Access, Project, and Power Point.
- Must be highly proficient in written and verbal communication.
Pay range: $75K-$95K Final compensation/salary will depend on experience
STAAR Surgical is an Equal Opportunity/Affirmative Action employer and all qualified applicants will receive consideration without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran or disability status, or any other characteristic protected by law. #USA
Job Roles at STAAR Surgical
Working at STAAR Surgical
STAAR Surgical's 12 open roles are mid to senior level, and about 0% are remote or hybrid. The most active teams are business analysis, cloud engineering, and data engineering. STAAR Surgical is a medical device company that develops and manufactures implantable ophthalmic products, including lenses used in vision correction surgery. The company operates across engineering, quality, clinical, regulatory, and corporate functions, with roles spanning production technicians, systems engineers, project managers, and legal counsel. Most STAAR Surgical roles are based in Lake Forest, with some in Monrovia and Aliso Viejo.
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Browse jobs by roleSTAAR Surgical Jobs: Frequently Asked Questions
How many jobs is STAAR Surgical hiring for right now?
STAAR Surgical is hiring for 12 open roles on Migrate Mate as of July 16, 2026, updated daily, concentrated in business analysis and cloud engineering. Open positions span engineering, quality assurance, information technology, clinical software, and corporate legal functions across the organization.
What kinds of roles does STAAR Surgical hire for?
The most active teams are business analysis, cloud engineering, and data engineering. STAAR Surgical hires across medical device engineering, quality control and assurance, IT systems and project management, clinical software product management, facilities operations, and corporate counsel. Most postings are mid to senior level, reflecting a mix of individual contributor and leadership positions across technical and business functions.
Are STAAR Surgical jobs remote or in-person?
Mostly on-site. About 0% of STAAR Surgical's open roles on Migrate Mate are remote or hybrid as of July 16, 2026, with the rest based in Lake Forest. Each STAAR Surgical listing shows its work location so you can filter before applying.
How do I apply to a job at STAAR Surgical?
Find a role that matches your background in STAAR Surgical's listings on Migrate Mate, then follow the link through to STAAR Surgical's own careers page to submit your application directly. STAAR Surgical manages its own hiring process, including application review, interviews, and offers.
What do STAAR Surgical jobs pay?
Listed salaries for STAAR Surgical roles on Migrate Mate range from about $75,000 to $270,000 per year as of July 16, 2026, with most postings at mid to senior level. Some roles list hourly contract rates. Exact pay is set by STAAR Surgical and shown on each listing.
Does STAAR Surgical hire entry-level?
Most of STAAR Surgical's open roles on Migrate Mate are mid to senior level as of July 16, 2026. Entry-level openings are limited. Check individual STAAR Surgical listings for stated experience requirements.
Where is STAAR Surgical hiring?
Most STAAR Surgical roles are based in Lake Forest, with some in Monrovia and Aliso Viejo, and about 0% offer remote or hybrid work as of July 16, 2026. Migrate Mate shows the location on each listing.