Validation Specialist (Contract) – QA & Compliance, Boston

Specialist Staffing Group; Boston (MA); On-site; USD 103,000 - 148,000; Full time

Job summary

Specialist Staffing Group in Boston, MA is seeking a contractor for Validation Specialist responsibilities to design and execute validation protocols aligned with regulatory requirements across engineering and life sciences domains.

You will conduct functional, performance, and safety testing, document results, and collaborate with manufacturing while maintaining traceability within quality systems. US work authorization is required.

Qualifications

• 2–5 years of validation, testing or quality assurance experience in engineering or life sciences environments.
• Working knowledge of testing protocols, quality management systems (QMS) and regulatory standards.
• Experience designing and executing test plans and documenting validation evidence.
• Strong attention to detail and ability to work methodically with technical documentation.
• Familiarity with manufacturing and field application contexts.
• Authorization to work in the United States.

Responsibilities

• Designing and executing validation protocols and test plans aligned with regulatory requirements and design standards
• Conducting functional, performance and safety testing across product lifecycles
• Documenting test results, validation reports and compliance evidence
• Collaborating with engineering and manufacturing teams to identify and resolve quality issues
• Supporting process validation and equipment qualification activities
• Maintaining detailed records and traceability for quality management systems
• Communicating validation findings and recommendations to cross-functional stakeholders

Skills

Validation experience

Testing protocols

Quality management systems

Regulatory standards knowledge

Documentation

Attention to detail

Education

ISTQB Certified Tester

Tools

CAD

Job description

Specialist Staffing Group in Boston, MA is seeking a contractor for Validation Specialist responsibilities to design and execute validation protocols aligned with regulatory requirements across engineering and life sciences domains.

You will conduct functional, performance, and safety testing, document results, and collaborate with manufacturing while maintaining traceability within quality systems. US work authorization is required.