At the Vitrolife Group, we work every day to unlock the full potential of science and technology to reduce the barriers towards building a family. Together we help our customers and their patients to fulfill the dream of having a baby.
Schedule: Monday through Friday, 6:30 AM - 3:00 PM
Location: Fully onsite cleanroom environment, San Diego, CA
Pay Rate: $25 - $28 / hr
Employment: Full-Time
Position Summary
The Production Team Lead coordinates first-shift production activities in a regulated medical device environment, working alongside the team to meet weekly output and quality goals. This is a hands-on working lead role, approximately 50-75% of time is spent in direct production using microscopes and semi-automated equipment, with the remainder dedicated to tracking key metrics (output per hour, yield), ensuring GMP/GDP compliance, supporting training, and managing shift logistics.
The ideal candidate brings a strong production background, a quality-first mindset, and the ability to lead by example on the floor.
Key Responsibilities
• Lead and coordinate day-to-day production activities of the first-shift production team
• Participate in manufacturing with the team while monitoring overall production goals
• Serve as first point of contact for production flow, issues, and escalation to management
• Manage information transfer between 1st and 2nd shift
• Ensure compliance with Good Manufacturing Practices (GMP) and related SOPs
• Monitor team documentation practices according to Good Documentation Practices (GDP)
• Support shift coverage, rotations, and breaks in coordination with management
• Lead departmental training activities and maintain compliant training records
• Drive continuous improvement in production and product quality with management
• Maintain accurate records and documentation per GDP and SOPs
• Track and implement corrective action protocols
• Troubleshoot robotics and automation equipment; coordinate advanced support as needed
• Reinforce workplace standards and company policies through modeling and communication
Required Qualifications
• 3 to 5 years of related manufacturing experience in a regulated medical device or electronics assembly environment
• Previous experience acting as a working lead, senior technician, or informal team lead supporting production teams
• Solid understanding of Good Documentation Practices (GDP), Good Manufacturing Practices (GMP), and Good Laboratory Practices (GLP)
• Familiarity with FDA regulations and quality processes
• Working knowledge of Microsoft Office and large Enterprise Resource Planning (ERP) systems
Preferred Qualifications
• Experience in production management, assembly, and process improvement
• Knowledge of cleanroom operations and medical device assembly
• Experience with robotics and automation
Work Environment