Quality Assurance Technician

Scorpion Therapeutics; Milwaukee (WI); On-site; USD 45,000 - 65,000; Full time

Job summary

Scorpion Therapeutics is seeking a QA support technician within the medical device QA department, focusing on batch release and compliance functions. Responsibilities include reviewing production documentation, assisting with batch release procedures, supporting regulatory documentation, and compiling monthly QA reports.

This role uses ERP systems and requires strong communication and attention to detail. This position is based in the United States (Wisconsin, Milwaukee) with a standard weekday

Qualifications

• Proficiency in Excel and Word for documentation and reporting.
• Strong communication skills and attention to detail are required.
• Experience with electronic management systems and ERP is preferred.

Responsibilities

• Review production documentation.
• Assist with batch release procedures.
• Support regulatory documentation registration.
• Compile monthly QA reports.
• Conduct QA activities using ERP systems.
• Liaise with operations to ensure regulatory and quality compliance.
• Support deviation and corrective action processes.
• Respond to quality queries.

Skills

Excel

Word

Electronic Management Systems

Communication skills

Attention to detail

Education

High School Diploma

Tools

ERP systems

Job description

Role

QA support technician within the medical device QA department, focusing on batch release and compliance functions.

Responsibilities

• review production documentation
• assist with batch release procedures
• support regulatory documentation registration
• compile monthly QA reports
• conduct QA activities using ERP systems
• liaise with operations to ensure regulatory and quality compliance
• support deviation and corrective action processes
• and respond to quality queries

Requirements

• High School Diploma or relevant experience
• proficiency in Excel, Word, and Electronic Management Systems
• strong communication skills, attention to detail

Preferred

• highly organized
• motivated
• interpersonal skills
• familiarity with eDHR system

High-Value

supporting product release, regulatory documentation, deviation management, quality reporting; applicable to medical devices; role involves routine QA activities, documentation review, cross-departmental liaison.

Work setup

standard weekday schedule, no travel specified, based in the United States, no visa sponsorship.