Supplier Quality Engineer

SaniSure; Camarillo (CA); On-site; USD 80,000 - 110,000; Full time

Job summary

SaniSure is seeking a Supplier Quality Engineer to ensure compliance of externally sourced materials in medical device manufacturing. This role will involve leading supplier audits and performance monitoring while collaborating cross-functionally with Supply Chain, R&D, and Operations.

The ideal candidate will have a Bachelor's degree and at least 5 years of quality experience in a regulated industry. Strong knowledge of FDA regulations is essential. Join us at SaniSure and contribute to the development of innovative biopharmaceuticals.

Qualifications

• Minimum 5 years of quality experience in a regulated industry.
• Experience conducting supplier audits independently.
• ASQ Auditor or Lead Auditor certification for ISO 13485 preferred.

Responsibilities

• Ensure externally sourced materials meet regulatory and quality requirements.
• Lead supplier selection, qualification, and compliance audits.
• Establish and maintain supplier performance metrics.

Skills

Quality experience in a regulated industry

Strong knowledge of FDA regulations and ISO standards

Supplier auditing practices

Technical writing and analytical skills

Education

Bachelor’s degree in biological sciences, engineering, or related field

Job description

About SaniSure

SaniSure is a high-growth multinational manufacturer of single-use products and systems used in the production of biological drugs, including cell therapies, gene therapies, and vaccines. With operations in the U.S. and Europe, we supply global pharmaceutical and biotech companies with the critical tools they need to develop and manufacture some of today’s most innovative and life-changing medicines. As we continue to expand our product offerings and global footprint, SaniSure offers an exciting opportunity to join a nimble, customer-focused company at the forefront of the biotech industry.

Job Summary

The Supplier Quality Engineer (SQE) is responsible for ensuring that externally sourced materials, components, and services meet applicable regulatory, quality, and performance requirements for medical device manufacturing. This role partners cross-functionally with Supply Chain, Manufacturing, R&D, and Regulatory Affairs to qualify, monitor, and continuously improve supplier performance in compliance with FDA 21 CFR Part 820 (QMSR), ISO 13485, and other global regulatory standards.

Supplier Qualification and Onboarding

• Lead supplier selection and qualification activities, including supplier audits (on-site and remote), quality system assessments, and technical capability evaluations.
• Approve supplier validation documentation and quality agreements.
• Establish supplier quality requirements and acceptance criteria.
• Ensure suppliers meet ISO 13485 and FDA QSR/QMSR expectations.

Supplier Auditing and Oversight

• Plan and execute supplier audits in accordance with risk-based audit schedules.
• Evaluate compliance to 21 CFR Part 820, ISO 13485, ISO 14971 (as applicable), and ISO 11135/11137 (for sterilization suppliers, if applicable).
• Document audit findings and drive timely corrective actions.
• Assess supplier readiness for regulatory inspections.

Supplier Performance Monitoring

• Establish and maintain supplier scorecards and KPIs.
• Analyze supplier quality trends (PPM, NCRs, SCARs, OTD, etc.).
• Drive continuous improvement initiatives with suppliers.
• Conduct quarterly business reviews as needed.

Nonconformance & CAPA Management

• Lead supplier corrective action requests (SCARs).
• Investigate supplier-related nonconformances and complaints.
• Perform root cause analysis (5‑Why, Fishbone, etc.).
• Verify effectiveness of corrective and preventive actions.
• Escalate critical quality issues appropriately.

Validation and Change Management Support

• Support supplier-related validation activities, including process validation (IQ/OQ/PQ), sterilization validation oversight, and packaging validation support.
• Review and approve supplier change notifications.
• Perform risk assessments for supplier changes.
• Ensure proper implementation through change control processes.
• Ensure compliance with biocompatibility, material, and regulatory requirements.
• Support regulatory submissions requiring supplier documentation.

Risk Management

• Participate in supplier risk assessments.
• Support DFMEA/PFMEA related to supplied components.
• Ensure critical suppliers are identified and controlled appropriately.

Cross-Functional Collaboration

• Partner with Engineering during new product development and with Operations during scale-up and product transfer.
• Provide supplier quality input during design reviews.
• Perform additional job duties as assigned.

Education

• Bachelor’s degree in biological sciences, engineering, or a related field.

Required Experience & Competencies

• Minimum 5 years of quality experience in a regulated industry.
• Strong knowledge of FDA 21 CFR Part 820 (QMSR), ISO 13485, Risk Management (ISO 14971), CAPA systems, and supplier auditing practices.
• Experience conducting supplier audits independently.
• Experience managing SCARs and supplier performance metrics.
• Strong technical writing and analytical skills.
• ASQ Auditor or Lead Auditor certification for ISO 13485 preferred.

Equal Employment Opportunity Policy

We are committed to providing equal employment opportunities to all employees and applicants without regard to race, religion (including religious dress and grooming practices), color, sex (including childbirth, breast feeding, and related medical conditions), gender identity or expression, sexual orientation, national origin, citizenship status, uniform service member status, pregnancy, age (40 and over), genetic information, disability (mental and physical), or any other protected status in accordance with all applicable federal, state, and local laws.