Associate QA Software Validation Engineer
- BioFire Diagnostics, Inc.
- Hazelwood, Missouri
- Full Time
Position Summary
bioMerieux is seeking an Associate QA Software Validation Engineer to support computer system validation (CSV) and non-product software quality activities at the St. Louis site. This role is ideal for an early-career quality or validation professional looking to build experience in a regulated manufacturing environment.
The Associate QA Software Validation Engineer will support validation initiatives, maintain the validated state of systems, and ensure compliance with applicable regulatory and internal quality standards.
Key Responsibilities
- Execute computer system and equipment validation activities under the guidance of validation leads.
- Develop, review, and execute validation protocols (IQ/OQ/PQ), test scripts, and reports.
- Review and approve validation lifecycle documentation including URS, risk assessments, GxP and ERES assessments.
- Support change control activities, ensuring system changes are properly evaluated and validated.
- Perform periodic reviews and requalifications to maintain the validated state of computer systems and equipment.
- Participate in anomaly and deviation resolution in collaboration with cross-functional teams.
- Support site non-product software risk assessments and FDA 21 CFR Part 11 compliance activities.
- Assist with CAPAs, investigations, waivers, and continuous improvement initiatives.
- Participate in QA oversight activities related to non-product software, MES, calibration, maintenance, and facilities.
- Maintain accurate validation files and documentation in accordance with site and global procedures.
- Perform all work in compliance with company quality policies, procedures, and regulatory requirements.
- Perform other duties as assigned.
Required Qualifications
- Bachelors degree required (Engineering, Computer Science, Life Sciences, or related field preferred), or
- 4 years of direct computer system validation experience in the pharmaceutical, biotechnology or medical device industry in lieu of degree.
- Ability to work in a regulated environment (pharmaceutical, biotechnology, medical device, or healthcare).
- Strong attention to detail and documentation skills.
- Proficiency with Microsoft Office tools (Outlook, Teams, Word, Excel).
Preferred Qualifications
- At least 1 year of computer system validation or quality engineering experience in a regulated industry.
- Basic knowledge of:
- FDA 21 CFR Part 820 and Part 11
- ISO 13485
- cGMPs and GAMP principles
- Understanding of validation and qualification concepts.
Key Competencies
- Strong written and verbal communication skills.
- Ability to manage priorities and meet deadlines in a fast-paced environment.
- Analytical thinking and problem-solving capabilities.
- Ability to work cross-functionally and collaboratively.
- High level of integrity, accountability, and attention to quality.
Working Conditions
- Primarily office and manufacturing environment.
- Ability to sit or stand for extended periods.
- Occasional movement throughout manufacturing areas and laboratories.
- Ability to lift up to 510 lbs.
- Minimal domestic or international travel required.