Manufacturing Technician II

Our Santa Clara, CA site is a center for the design, development and manufacturing of innovative bioprocessing equipment and automation solutions that support the production of biologic medicines and vaccines. Our technologies—including single-use bioreactors, mixers, fermenters, chromatography systems, centrifuges and process control software—help biopharmaceutical manufacturers improve efficiency, scale production and accelerate the delivery of life-changing therapies.

About the role

The Manufacturing Technician II performs manufacturing, assembly, testing, and verification activities for single-use technologies and related control systems within a regulated production environment. This role contributes to business performance by ensuring product quality, schedule adherence, operational efficiency, and right-first-time execution across manufacturing processes. The position maintains compliance with GMP, safety, and documentation requirements while supporting continuous improvement initiatives and cross-functional production objectives.

Responsibilities

• Perform manufacturing processes, assembly, testing, rework, and build functional verification/testing (BFV) activities following SOPs, work instructions, and production requirements.
• Build, test, program, modify, troubleshoot, and repair equipment and components including VABs, TruLogic systems, thin clients, pump towers, controllers, transmitters, cables, hoses, and Mass Flow Controller Assemblies.
• Stage systems for integration, testing, validation, teardown, and final quality inspection.
• Assemble, clean, maintain, and prepare equipment as required to support production activities.
• Support Factory Acceptance Testing (FAT), validation activities, and final product verification as needed.
• Execute manufacturing and testing activities in accordance with production schedules, work order requirements, and quality standards to achieve right-first-time execution.
• Complete production tasks accurately, safely, and within established timelines while minimizing errors, rework, and production delays.
• Ensure equipment and assemblies consistently meet functional, quality, and performance requirements.
• Complete travelers, production records, and related documentation accurately and in compliance with GMP, safety, quality, and data integrity requirements.
• Identify, troubleshoot, communicate, and support resolution of production issues, deviations, and non-conformances; escalate issues as appropriate.
• Maintain a clean, safe, organized, and audit-ready work environment.
• Support production planning and work order requirements, including material staging and parts issuance as needed.
• Collaborate with Planning, Integration, Validation, Quality, Logistics, and Engineering teams to support production schedules and customer requirements.
• Participate in cross-training, knowledge sharing, and Practical Process Improvement (PPI) initiatives to improve efficiency, quality, and workflow.
• Communicate effectively with team members and stakeholders to support operational continuity and timely resolution of production-related issues.
• Perform other duties as assigned.

Requirements

• High school diploma or equivalent.
• 1 year of experience in a manufacturing, production, assembly, or operations environment.
• Experience in performing manufacturing, assembly, testing, troubleshooting, or equipment-related activities.
• Experience following SOPs, work instructions and production documentation requirements.
• Experience working in a safety-focused environment with strong attention to quality and compliance.

Preferred Qualifications

• Experience in a GMP-regulated manufacturing environment.
• Experience with single-use technologies, industrial control systems, or bioprocess equipment.
• Experience supporting validation, Factory Acceptance Testing (FAT), quality inspections, or continuous improvement initiatives.

Skills

• Understanding of GMP, safety, quality, and data integrity requirements within a regulated manufacturing environment.
• Ability to read and interpret work instructions, standard operating procedures (SOPs), Bills of Materials (BOMs), schematics, layout drawings, and technical documentation.
• Strong attention to detail with the ability to maintain accuracy in manufacturing, testing, and documentation activities.
• Ability to accurately complete production records, travelers, and related documentation.
• Ability to use common hand tools, electrical test equipment, and measurement devices to perform assembly, testing, troubleshooting, and repair activities.
• Ability to work independently and collaboratively in a fast-paced team environment.
• Strong organizational and time management skills with the ability to manage multiple priorities and meet production schedules.
• Proficiency with Microsoft Office applications, including Word, Excel, and Outlook.
• Commitment to safety, quality, compliance, and continuous improvement.

Preferred Skills

• Knowledge of single-use technologies, bioprocess equipment, or industrial control systems.
• Familiarity with controller and transmitter programming and configuration.
• Experience with ERP systems such as Agile, SAP, or similar manufacturing systems.
• Knowledge of Factory Acceptance Testing (FAT), validation activities, and quality inspection processes.
• Familiarity with electronic documentation systems and quality management systems.
• Understanding of Practical Process Improvement (PPI), Lean Manufacturing, or continuous improvement methodologies.

Work Environment

• Primarily works in a manufacturing and production environment with regular exposure to assembly, testing, and equipment-related activities.
• Prolonged standing and walking throughout the work shift while performing manufacturing, assembly, testing, and inspection activities.
• Frequent bending, kneeling, crouching, reaching, and working in confined or difficult-to-access areas to support equipment assembly, troubleshooting, and maintenance.
• Frequent use of manual dexterity and fine motor skills to assemble, test, modify, troubleshoot, and repair equipment and components.
• Regular use of hand tools, power tools, electrical test equipment, and measurement devices.
• Ability to work around large process systems and equipment during assembly, integration, testing, and validation activities.
• Ability to lift and move materials, components, and equipment up to 25 lbs. unassisted and up to 30 lbs. with appropriate assistance or lifting equipment.
• Ability to work on elevated platforms and operate scissor lifts when properly trained and certified.
• Exposure to manufacturing equipment, moving mechanical parts, and moderate noise levels in a production environment.
• Required use of personal protective equipment (PPE), including safety shoes, hard hats, safety glasses, gloves, and other PPE as required by the work area.
• Ability to work safely in accordance with company safety policies, procedures, and regulatory requirements.
• Adherence to all Good Manufacturing Practices (GMP) and safety standards.
• May be required to work overtime, flexible schedules, or adjusted shifts to support production demands and business needs.

Schedule

Monday through Friday, 7:00 am to 3:30 pm.

Pay

The hourly pay range estimated for this position based in California is $26.00–$30.00. This position may also be eligible to receive a variable annual bonus based on company, team, and/or individual performance results in accordance with company policy.

Benefits

• A choice of national medical and dental plans, and a national vision plan, including health incentive programs.
• Employee assistance and family support programs, including commuter benefits and tuition reimbursement.
• At least 120 hours paid time off (PTO), 10 paid holidays annually, paid parental leave (3 weeks for bonding and 8 weeks for caregiver leave), accident and life insurance, and short- and long-term disability in accordance with company policy.
• Retirement and savings programs, such as our competitive 401(k) U.S. retirement savings plan.
• Employees’ Stock Purchase Plan (ESPP) offers eligible colleagues the opportunity to purchase company stock at a discount.