Reagent Manufacturing Technician - IVD & Scale-Up

Pattern Bioscience, Inc.; Austin (TX); On-site; USD 25,000 - 39,000; Full time

Job summary

Pattern Bioscience, Inc. seeks a reagent manufacturing associate to deliver manufacturing and testing in an IVD environment, with documentation and process control responsibilities.

You will support new product design transfers, stability studies, and method development, while ensuring equipment validation and quality standards are met. The role requires an Associate degree in life sciences or related field, hands-on lab experience with pipetting and HPLC, and proficiency with Word/Excel.

Qualifications

• Associate degree with hands-on lab experience in IVD manufacturing.
• Experience with pipetting and documentation.
• Familiarity with ISO 13485 and FDA QSR requirements.

Responsibilities

• Deliver reagent manufacturing and testing requirements for IVD environment.
• Complete process documentation and related business system transactions.
• Participate in product design transfer, stability studies, and method validations.
• Support experimental plans with parameter adjustments and observations.
• Assist in projects targeting efficiency, scaling, and quality improvements.
• Update work instructions, SOPs, and change controls.
• Assist investigations and CAPA closures from audits or customer feedback.
• Coordinate activities within a team and communicate effectively.
• Deliver maintenance and calibration of measuring devices.

Skills

Mathematics aptitude

Attention to detail

Critical thinking

Problem solving

Self-directed work style

Team collaboration

Education

Associate degree in Life Sciences, Chemistry, or Medical Technology

Tools

HPLC

Pipetting

ISO 13485 knowledge

FDA Quality System understanding

Enterprise Manufacturing systems

Job description

Pattern Bioscience, Inc. seeks a reagent manufacturing associate to deliver manufacturing and testing in an IVD environment, with documentation and process control responsibilities.

You will support new product design transfers, stability studies, and method development, while ensuring equipment validation and quality standards are met. The role requires an Associate degree in life sciences or related field, hands-on lab experience with pipetting and HPLC, and proficiency with Word/Excel.