Factory Service Engineer

Cellares; South San Francisco (CA); On-site; USD 90,000 - 210,000; Full time

Job summary

An innovative company is seeking a motivated Factory Service Engineer to ensure optimal performance of manufacturing equipment in a GMP environment. This hands-on role involves performing preventative maintenance, troubleshooting, and collaborating with cross-functional teams to uphold quality standards. With opportunities for growth and a commitment to continuous improvement, this position offers a dynamic work environment where your contributions are valued. Join a forward-thinking organization that is revolutionizing cell therapy manufacturing and making a significant impact on patient care.

Benefits

Highly subsidized Medical, Dental, and Vision Plans

401(k) Matching

Free EV Charging

Onsite lunches

Stock options

Qualifications

• 5+ years in a GMP manufacturing environment, preferably in cell therapy.
• Strong understanding of GMP regulations and quality standards.

Responsibilities

• Perform installations, maintenance, and troubleshooting of GMP equipment.
• Collaborate with teams to ensure compliance with GMP standards.
• Respond to equipment failures and implement corrective actions.

Skills

GMP Compliance

Troubleshooting

Preventative Maintenance

Calibration

Technical Documentation

Communication Skills

Team Collaboration

Education

Associate Degree in Engineering

Tools

Computerized Maintenance Management System (CMMS)

Job description

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We are seeking an innovative and highly motivated service engineer who will contribute significantly to the success of service maintenance, repair, and support for Cellares with their equipment.

The primary focus of this position will be to perform preventative maintenance, repairs, calibration, and troubleshooting of GMP Cellares process equipment. This is a hands-on position and local to the South San Francisco, CA facility.

Candidates should enjoy working in a fast-paced, mission-driven environment and be prepared to tackle a broad selection of challenges as the company grows. This role will primarily be in our South San Francisco, California, facility, with up to 20% travel to our Bridgewater, New Jersey, and other Cellares locations.

Responsibilities

• Perform installations, routine maintenance, and troubleshooting of Cellares and other process equipment within a Good Manufacturing Practice (GMP) environment in a cell therapy manufacturing facility
• Collaborate with cross-functional teams to ensure compliance with GMP standards and regulations
• Perform equipment calibrations and support validation testing to meet quality and regulatory requirements
• Respond promptly to equipment failures and implement corrective actions to minimize downtime.
• Execute preventative maintenance activities to ensure optimal functionality of manufacturing equipment
• Support the installation and qualification of new equipment, ensuring adherence to GMP guidelines
• Support the facilities team in providing maintenance and repair in the GMP environment as needed
• Maintain accurate documentation of all maintenance activities and equipment logs in a Computerized Maintenance Management System (CMMS)
• Manage parts ordering and coordinate with equipment and area owners to schedule maintenance activities
• Maintain tools and test equipment, and ensure they are properly calibrated and in good, safe working condition
• Collaborate with manufacturing and quality control teams to address technical issues and optimize processes
• Support Quality Change Controls and CAPA investigations
• Stay updated on industry trends and advancements to contribute to continuous improvement initiatives
• Participate in training programs to enhance technical skills and knowledge
• After hours, On-Call rotation for support of the GMP facility is required through PagerDuty
  
  

Requirements

• Associate degree or equivalent in engineering or a related field
• 5+ years’ experience in a GMP manufacturing environment, preferably in cell therapy or biopharmaceuticals
• Strong understanding of GMP regulations and quality standards
• Proficient in troubleshooting and repairing complex manufacturing equipment
• Ability to read and understand technical documents and engineering drawings
• Excellent organizational and documentation skills
• Ability to work collaboratively in a team-oriented environment
• Effective communication skills to interact with diverse stakeholders
• Must be able to work 40 hours a week, which may include swing shifts, weekends, holidays, etc.
• Attendance at the plant site is considered an essential function
• Detail-oriented with a commitment to maintaining high-quality standards
• Ability to lift and carry up to 50 lbs
• Excellent verbal, written, organizational, presentation, and interpersonal skills
• Self-awareness, integrity, authenticity, and a growth mindset.
  
  

$90,000 - $210,000 a year

Cellares total compensation package contains competitive base salaries, highly subsidized Medical, Dental, and Vision Plans, 401(k) Matching, Free EV Charging, Onsite lunches, and Stock options. All displayed pay ranges are approximate, negotiable, and location dependent.

This is Cellares

Cellares is the first Integrated Development and Manufacturing Organization (IDMO) and takes an Industry 4.0 approach to mass manufacturing the living drugs of the 21st century. The company is both developing and operating integrated technologies for cell therapy manufacturing to accelerate access to life-saving cell therapies. The company’s Cell Shuttle integrates all the technologies required for the entire manufacturing process in a flexible and high-throughput platform that delivers true walk-away, end-to-end automation. Cell Shuttles will be deployed in Cellares’ Smart Factories around the world to meet total patient demand for cell therapies at global scale. Partnering with Cellares enables academics, biotechs, and pharma companies to accelerate drug development and scale out manufacturing, lower process failure rates, lower manufacturing costs, and meet global patient demand.

The company is headquartered in South San Francisco, California with its commercial-scale IDMO Smart Factory in Bridgewater, New Jersey. The company is backed by world-class investors and has raised over $355 million in financing.

Leveling will be based on overall experience, education, and demonstration of knowledge throughout the interview process.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Engineering and Information Technology

• Industries

  Pharmaceutical Manufacturing

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