Quality Auditor III

Job Title: Quality Auditor III

Location: Andover, MA

Type: Contract

Compensation: $55-$60.83/hr

Work Model: Onsite

Hours: 8am to 5pm MF

Overview

Our client is seeking a QAV Validation & Digital Specialist to support a strategic quality and digital transformation initiative. This role will initially focus on Quality Assurance Validation activities and will transition into a digital quality-focused function as project needs evolve.

The ideal candidate will bring experience in digital quality systems, electronic documentation management, or manufacturing digitalization initiatives and be willing to learn and support validation processes within a regulated environment. Comprehensive training on company procedures, quality systems, and validation requirements will be provided.

Responsibilities

• Initial QAV Validation Responsibilities
• Review protocols, change controls, SOPs, and validation documentation.
• Support compliance assessments and documentation review activities.
• Conduct quality reviews to ensure adherence to internal procedures and regulatory requirements.
• Participate in validation project execution and documentation management.
• Future Digital Quality Responsibilities
• Support digital quality initiatives and electronic quality management processes.
• Review and manage electronic batch records and associated documentation.
• Utilize digital quality platforms and software tools to support quality operations.
• Assist with system implementation, optimization, and data-driven quality improvements.
• Partner with cross-functional teams to enhance digital workflows and process efficiencies.

Requirements

• Bachelor's degree in Engineering, Life Sciences, Information Systems, Computer Science, or a related field.
• Experience working with digital quality systems, electronic documentation systems, manufacturing systems, or related digital platforms.
• Strong technical aptitude with the ability to learn validation and quality processes.
• Excellent organizational, analytical, and communication skills.
• Ability to adapt to evolving project requirements and responsibilities.

Preferred

• Experience in pharmaceutical, biotechnology, medical device, or regulated manufacturing environments.
• Familiarity with electronic batch records, quality management systems, or validation activities.
• Experience supporting digital transformation, process automation, or data management initiatives.
• Exposure to systems such as electronic documentation platforms, manufacturing execution systems (MES), or similar quality technologies.

System One, and its subsidiaries including Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

Ref: #558-Scientific