Join our highly motivated, mission-driven Manufacturing team as Manufacturing Associate II at Endologix!

WHO WE ARE: 

Endologix LLC is a California-based global medical device company dedicated to improving patients’ lives through innovative therapies for the interventional treatment of vascular disease. Our therapeutic portfolio addresses clinically relevant unmet needs, spanning from abdominal aortic aneurysms to lower limb peripheral vascular disease. We are committed to delivering excellent clinical outcomes through precision in product design, advanced manufacturing, and comprehensive physician training—supported by industry-leading clinical evidence. At Endologix, we’re driven by purpose, innovation, and the opportunity to make a lasting impact in vascular health.

We’re looking for a Manufacturing Associate II to join our manufacturing team. In this role, you’ll be responsible for assembling high quality medical devices in accordance with approved manufacturing process instructions and Standard Operating Procedures, assisting in the evaluation and resolution of line issues, and suggesting possible method / process improvements.

WHAT YOU'LL DO:

• Adhere to safety rules, stretching exercises, and company policies and procedures.
• Assemble product as required utilizing small hand tools, calibrated instruments, measurement equipment, microscopes, and test fixtures.
• Identify and communicate any safety, quality, process issues or concerns as needed.
• Maintain controlled environment integrity by using proper attire and adherence to controlled environment practices and procedures.
• Perform in-process quality checks as required while giving timely feedback as issues arise
• Recognize and report any unacceptable materials and/or sub-assemblies to engineering and/or supervisor.
• Responsible for 100% compliance to Endologix Quality and Regulatory policies and adhere to Endologix Core Values.
• Responsible for quality of work and adhering to manufacturing methods and quality records.
• Understand and comply with Good Manufacturing Practices (GMP) and Good Documentation Practices (GDP).
• Work with supervisors, engineers and technicians to resolve line issues and suggest improvements.
• Participate in lean activities and 5S improvement efforts.
• Be familiar with terminology used in the production area.
• Aware of common defects within manufacturing departments and the results caused by variations during the manufacturing processes.
• Capable of moving from one station to another without continuous mistakes.
• May be certified as a trainer and train other production employees on manufacturing processes.
• Capability to read and interpret engineering drawings, specs and method sheets.
• Electronic systems entry.
• Perform other duties as assigned by supervisor.

WHAT YOU'LL BRING:

Education:

• High school diploma or GED required.
• Associate degree in life sciences, engineering, or related field preferred.
• Additional coursework or certification in medical device manufacturing, GMP, or quality systems is a plus.

Experience:

• 2–4 years of hands-on experience in medical device manufacturing, pharmaceutical production, or other regulated life sciences industry.
• Proven experience working in a cleanroom environment and following aseptic techniques.
• Demonstrated history of performing manual assembly of small, intricate components under a microscope.
• Experience maintaining compliance with FDA, ISO 13485, and GMP regulations.
• Documented use of Device History Records (DHRs), batch records, or other controlled documentation systems.
• Track record of consistently meeting production, quality, and safety targets.
• Prior exposure to in-process quality inspection, measurement tools, and defect identification.
• Experience training or mentoring less experienced team members preferred.
• Familiarity with ERP/MES systems for production tracking and reporting.

Skills/Competencies:

• Knowledge of Good Manufacturing Practices (GMP) and ISO 13485 quality standards for medical device manufacturing.
• Ability to follow Standard Operating Procedures (SOPs), work instructions, and batch records with high attention to detail.
• Proficiency in using hand tools, fixtures, microscopes, and precision measurement equipment for assembly and inspection.
• Strong understanding of cleanroom protocols, gowning procedures, and contamination control.
• Demonstrated ability to perform repetitive tasks with consistency and accuracy in a regulated environment.
• Basic mechanical aptitude and ability to identify and troubleshoot minor equipment or process issues.
• Competence in documenting production activities clearly and accurately in Device History Records (DHRs).
• Good computer literacy (MS Office, ERP/MES systems preferred) for data entry and process tracking.
• Effective communication skills and ability to work collaboratively within cross-functional production teams.
• Strong problem-solving, time management, and organizational skills to meet production schedules and quality standards.
• Ability to train and mentor entry-level manufacturing associates as needed.
• Flexibility to work in a fast-paced environment with changing priorities and shift schedules.

HOW YOU'LL SHOW UP:

All In: Bring full commitment to everything you do. Support one another, hold yourself accountable, and take ownership of your work. Move with urgency, deliver on your promises, and lead with boldness and passion.

Act with Integrity: Prioritize ethics and transparency in every decision. Earn trust by being honest, respectful, and dependable — working diligently to uphold the confidence of your colleagues, customers, and communities.

Tenacious: Meet challenges head-on with resilience and resolve. Stay focused, push through obstacles, and consistently look for solutions, not excuses.

Pioneering: Challenge the status quo and embrace innovation. Develop new ideas, test bold solutions, and pave the way for others — driving progress through curiosity and creativity.

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:

• Hourly rate of $21.63/hr-$26.64/hr
• Equity participation as approved by Board of Directors (4-year vesting schedule)
• Comprehensive health, dental, and vision insurance plans
• Generous PTO and holiday schedule
• 401(k) retirement plan with company match

Plus:

• Employee wellness initiatives and mental health support
• Collaborative and inclusive company culture focused on impact and innovation
• Opportunities for career growth and internal mobility

OUR COMMITMENT TO DIVERSITY AND INCLUSION:

Endologix LLC.  is an Equal Opportunity 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.