Process Engineer II

Corporate Overview

Argonaut Manufacturing Services Inc. is a contract manufacturing organization (CMO) headquartered in Carlsbad, CA with over 100,000 square feet of manufacturing space across four locations. The company is dedicated to serving highly innovative companies in the biopharmaceutical and molecular diagnostics industries. Argonaut is a full service, cost‑effective partner, providing complete solutions in the areas of formulation, filling and final kitting of reagents and consumables.

Argonaut provides quality and regulatory expertise to assure the highest in quality manufacturing and supply chain excellence.

At Argonaut Manufacturing Services we value our employees and are proud to offer a comprehensive benefits package designed to support your well‑being and financial future. Eligible employees enjoy:

• Medical, Dental, and Vision Insurance
• Company‑Paid Life Insurance (1x Annual Salary)
• Voluntary Life Insurance Options
• Short‑Term and Long‑Term Disability Insurance
• Flexible Spending Account (FSA) & Health Savings Account (HSA)
• 401(k) Retirement Plan with Company Matching
• 10 Days of Paid Time Off (PTO)
• 10 Paid Holidays Annually

The pay range for this position is $95,000 - $105,000 annually. Actual compensation will be based on factors such as location, skills, education, experience, and other relevant qualifications.

This position reports to the Director of Technical Operations and will be responsible for providing expertise and guidance in the field of reagent formulation, filling and finishing activities for the Molecular Diagnostics & Life Sciences manufacturing segment of Argonaut Manufacturing Services. This individual will be hands‑on and be directly involved with floor technicians to ensure proper techniques and guidelines are being followed.

This role is an on‑site position Monday - Friday 8 hours/day (excluding lunch break). Overtime, weekends, and holidays may be required. Flexible start time between 7:00 am - 9:00 am with a consistent schedule.

• Develop and validate methods associated with QC and Manufacturing processes
• Design, specify and validate equipment and processes
• Design and execute experiments to support process changes
• Facilitate transition of new methodologies into manufacturing laboratory
• Troubleshoot existing processes and provide guidance on potential enhancements
• Perform IQ, OQ, and PQ for laboratory instruments
• Respond to process and instrument failures to minimize downtime
• Improve formulation processes and procedures
• Review and support the transfer of client process steps for formulation/filling and improve, when possible
• Responsible for development and implementation of production and analytical "In‑process" controls for commercial manufacturing
• Responsible for leading and executing transfer of NPIs from development to manufacturing shopfloor
• Responsible for independently designing and executing experimental protocols, interpreting data from different sources/format and preparing scientific/operations development reports
• Effective communication with all levels of organizational structure, through multiple departments
• Responsible for leading quality investigations like deviations, CAPAs, NCMRs, OOS, OOT issues
• Take initiative to develop and implement new processes to collect data around and analyze the health of production areas
• Create and format technical documents like SOPs, master batch record and work instructions
• Assist in defining technical requirements for new products
• Responsible for identifying and on‑boarding laboratory/floor equipment
• Characterize and develop key metrics to drive efficiency and robustness improvements in product development
• Collaborate with Development, Equipment engineering, Quality, Manufacturing, supply chain, and other departments as needed to address issues with and set appropriate specifications for manufactured products

• Bachelor's degree in Biology, Engineering, or Computer Science or related field and 4 or more years of experience in industrial setting
• Knowledge of ISO 13485 Quality Management System and GMP
• Must be meticulous and organized with excellent…