Production Supervisor

Endologix; Santa Rosa (CA); Sur place; USD 100 000 - 113 000; Plein temps

Avantages offerts par ce poste

Health, dental, and vision insurance

Discretionary bonus

Equity participation

401(k) with company match

Generous paid time off

HSAs/FSAs

Commuter benefits

Résumé du poste

Endologix is seeking a Production Supervisor in Santa Rosa, CA to lead manufacturing personnel and ensure high-quality output for our vascular care products. The role drives production schedules, safety, and continuous improvement within a cleanroom environment.

You will oversee daily operations, enforce GMP/QSR standards, manage attendance, and collaborate with Planning, Quality, and Engineering to meet metrics and timelines.

Qualifications

• Minimum 1 year Manufacturing Supervisor experience (Medical Device preferred).
• 6+ years of related manufacturing leadership experience (Internal Candidates).
• Experience working with manufacturing/ERP systems (QAD preferred).
• Knowledge of quality system requirements (QSR) and GMP.

Responsabilités

• Supervise production personnel and activities to meet customer requirements across commercial products, new product introductions, and clinical builds, ensuring outputs support high-quality patient outcomes.
• Lead the team in achieving production goals across Safety, Quality, Service, and Cost.
• Champion a culture of safety and accountability by promoting an injury-free work environment and high morale.
• Ensure compliance with FDA, GMP, QSR, ISO and company policies; manage non-conformances and corrective actions.
• Track, analyze, and communicate key performance metrics to drive continuous improvement.
• Forecast material, tool, and supply requirements to maintain production flow and readiness.
• Support ERP-related activities and accurate work order data entry; coordinate with Planning.

Connaissances

ERP Systems

QSR GMP

Cleanroom

MS Office

Formation

High school diploma or equivalent

Supervisor certification or AA preferred

Outils

QAD

Description du poste

Overview

Position: Production Supervisor

Department: Manufacturing

Location: Santa Rosa, CA

WHO WE ARE:

Endologix LLC operates asais a subsidiary of Rhevera Medical Holdings, LLC, a global medical device company focused on preserving and restoring the blood flow patients depend on. Our innovative vascular portfolio spans aortic repair, peripheral arterial disease, and thrombectomy, including the ALTO® Abdominal Stent Graft System, AFX®2 Endovascular AAA System, DETOUR™ System, and Pounce™ Thrombectomy System.

At Rhevera Medical, innovation is more than what we create. It’s how we think, collaborate, and move patient care forward. We’re building a mission-driven culture where your ideas matter, your growth is supported, and your work can make a meaningful difference.

Our Core Valuesguide the choices we make and the way we work, because our customers and patients depend on us:

• Patient Outcomes Drive Us:We improve lives with every advancement we deliver.
• Integrity Defines Us:We do what’s right, stay transparent, prioritize quality, and own our actions.
• Innovation Advances Us:We stay curious, adaptable, and push boundaries.
• Boldness Propels Us:We take smart risks and are unafraid in our pursuit of excellence.
• Collaboration Unites Us:We partner across teams and with physicians to drive exceptional results.

Ready to bring your ideas, experience, and passion to work that matters? Join us and help shape what’s next in vascular care.

Employment with Endologix LLC: Candidates applying for this position are applying for employment with Endologix LLC, which operates as a Rhevera Medical company. Candidates for this role will not be employed, or jointly employed, by Rhevera Medical Holdings, LLC.

ABOUT THE ROLE:

The Production Supervisor is responsible for providing leadership to manufacturing personnel to produce high quality products for our customers. Responsibilities include direct management of production personnel, fulfillment of the production schedule, and ensuring quality compliance. Provide operations expertise to the supervision and support of manufacturing personnel to achieve New Product Development, Continuous Improvement, Quality, Compliance and Operational metrics. Supervise the activities of employees in the production area. Ensure that daily production schedules are met, manufacturing procedures are followed, and all production personnel are trained in those procedures. Ensure fair and equitable treatment of all employees by following company policies and department guidelines.

Responsibilities

WHAT YOU'LL DO:

• Supervise production personnel and activities to consistently meet customer requirements across commercial products, new product introductions, and clinical builds, ensuring every output supports high-quality patient outcomes.
• Lead the team in achieving production goals across Safety, Quality, Service, and Cost, fostering a results-driven environment that balances operational excellence with smart, forward-thinking decision-making.
• Champion a culture of safety, accountability, and respect by promoting an injury-free work environment, maintaining high employee morale, and reinforcing adherence to standards and best practices.
• Ensure full compliance with quality systems (FDA, GMP, QSR, ISO), product specifications, and company policies, upholding integrity through disciplined execution and transparent management of non-conformances and corrective actions.
• Continuously challenge processes and team performance to deliver efficient, cost-effective solutions, encouraging innovation and calculated risk-taking to improve outcomes.
• Establish clear performance expectations, drive accountability, and recognize contributions, fostering a collaborative team environment built on trust and shared success.
• Administer and execute company policies and procedures consistently, ensuring alignment across individuals and team structures.
• Track, analyze, and communicate key performance metrics, leveraging data-driven insights to guide decisions and drive continuous improvement.
• Maintain timecards and attendance records, proactively planning for coverage needs and adapting to workforce fluctuations with agility.
• Effectively manage shifting priorities and competing demands, demonstrating flexibility and resilience in a dynamic production environment.
• Proactively identify and mitigate potential failure modes related to quality or business risks, reinforcing a culture of ownership and continuous improvement.
• Recruit, develop, and retain top production talent, building a high-performing team equipped to meet evolving business and customer needs.
• Assess and address training needs, ensuring employees are fully prepared and confident before undertaking responsibilities.
• Drive lean manufacturing initiatives to enhance quality, improve productivity, reduce costs, and streamline cycle times, while empowering the team through education and engagement.
• Forecast material, tool, and supply requirements, coordinating effectively to ensure seamless production flow and operational readiness.
• Support ERP-related activities, including accurate entry of work order information as needed.
• Monitor inventory levels and collaborate closely with Planning to ensure alignment and efficiency in daily operations.
• Troubleshoot operational challenges with urgency and accountability, working cross-functionally to resolve issues and prevent recurrence.
• Contribute to the development and implementation of new procedures and processes, supporting innovation and successful product introductions.
• Create, review, and approve document change orders, ensuring accuracy, compliance, and alignment with production needs.
• Conduct regular performance evaluations, providing constructive feedback and identifying development opportunities to support individual and team growth.
• Operate effectively within a clean room environment, maintaining strict adherence to protocols and quality standards.
• Perform other duties as assigned, demonstrating adaptability, ownership, and a commitment to team and organizational success.

Qualifications

WHAT YOU'LL BRING:

Education:

• High school diploma or equivalent.
• Supervisor certification or AA preferred.

Experience:

• 1 year Manufacturing Supervisor experience (Medical Device preferred).
• 6+ years of related manufacturing experience in a leadership role (Internal Candidates).

Skills/Compentencies:

• Experience working with manufacturing/ERP systems (QAD preferred).
• Working knowledge of quality system requirements (QSR) and good manufacturing practices (GMP).
• Experience working in a cleanroom environment and application of environmental procedures.
• Experience with Microsoft Office or similar computer software.

WHAT WE OFFER:

At Endologix, we know that great work starts with great people — and people do their best when they feel valued and supported. That’s why we offer competitive pay, solid benefits, career growth, a culture that genuinely cares, and the flexibility you need to thrive both at work and at home. But more than that, we offer purpose. You’ll be part of a team that’s making a real impact on patients’ lives. When you join us, you’re not just taking a job, you’re building a meaningful career with a team that’s invested in your success.

The compensation package includes:

• Base salary of $100,000/yr-$112,500/yr
• Discretionary bonus
• Equity participation as approved by Board of Directors (4-year vesting schedule)
• Comprehensive health, dental, and vision insurance plans
• Flexible Health Savings Accounts (HSAs) and/or Flexible Spending Accounts (FSAs)
• Generous paid time off (vacation, sick leave, holidays, and flexible time off that is available for Exempt employees)
• 401(k) retirement plan with company match

Plus:

• Employee wellness initiatives, mental health resources, and Employee Assistance Program (EAP)
• Employee recognition programs and awards
• Commuter benefits or transportation stipends

OUR COMMITMENT TO EQUAL OPPORTUNITY & VETERAN INCLUSION:

Endologix LLC, which operates asa Rhevera Medical company, is an Equal Opportunity and Affimation Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, disability, protected veteran status, or any other characteristic protected by applicable federal, state, or local law. As a federal contractor, Endologix LLC is committed to taking affirmative action to recruit, employ, and advance in employment qualified individuals with disabilities and protected veterans.