Twist Bioscience

Biotechnology

EquipmentEngineer

$105–128k South San Francisco, California, United States
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“Equipment Engineer at Twist Bioscience. Skills: Equipment validation, Preventative maintenance, Troubleshooting. Lead equipment validation. Execute IQ, OQ, PQ”

What You'll Achieve.

Minimize downtime; Reduce downtime; Eliminate downtime

Industry & Context.

Biotechnology
Problems you'll solve

Problem-solver; Troubleshooting

Eligibility Requirements

Work in cleanroom

What They're Looking For.

Must Have

5+ years production instrumentation experience, Experience with automated liquid handlers, Experience with robotics, Experience with MES/LIMS integration, Good computer skills, Ability to learn new software

Nice to Have

Experience working under ISO 9001, Experience working under ISO 13485, Experience working under GMP/cGMP standards

What You'll Do.

Lead equipment validation

Manage preventative maintenance

Execute routine maintenance

Investigate equipment failures

Implement engineering fixes

Ensure timely CAPA closure

Ensure timely Change Control closure

Multi-task in dynamic environment

Work in cleanroom setting

Draft technical documentation

Manage maintenance records

How You'll Work.

Team & Collaboration

Collaborative approach

Communication Scope

Interpersonal skills; Documentation experience

Process & Methodology

CAPA management, Change control management

Full Job Description

Equipment Engineer (onsite in South San Francisco, CA ) Job Description The Equipment Engineer is responsible for ensuring the reliability and performance of all production instrumentation within a high-throughput DNA synthesis environment. You will be the primary lead for validating equipment, performing routine and preventative maintenance, and executing complex troubleshooting to minimize downtime.The ideal candidate is a self-motivated problem-solver who thrives in a fast-paced setting and is committed to maintaining the rigorous quality metrics required for cutting-edge biotechnology production. What You’ll Be Doing Equipment Validation: Lead the execution of Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) for both new and existing instrumentation. Preventative Maintenance: Manage the scheduling and execution of routine maintenance and calibrations in strict accordance with manufacturer specifications and internal quality standards. Troubleshooting: Investigate recurring equipment failures to implement permanent engineering fixes, significantly reducing or eliminating downtime. Quality Compliance: Own and ensure the timely closure of equipment-related CAPAs (Corrective and Preventive Actions) and Change Controls. Inventory experience working under ISO 9001, ISO 13485, or GMP/cGMP standards is highly preferred. Adaptability: Ability to multi-task in a dynamic environment and work comfortably in a cleanroom setting (requiring lab coats, hairnets, and gloves). Good computer skills (Excel, Word, Atlassian etc) and the ability to quickly learn new software applications. Communication: Excellent interpersonal skills with a collaborative approach to problem-solving. Strong documentation experience, drafting technical documentation, and managing maintenance records. Bonus Assets: Experience with automated liquid handlers, robotics, or MES/LIMS integration is a significant plus. About Twist Bioscience Twist Bioscience

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