Job Title: Instrument Software Validation Engineer
Location- Remote (Travel required on and as needed basis to KY)
Duration: 6 Months
 
Key Responsibilities:

• Document and validate software installed on lab instruments per EMA regulatory standards.
• Validate Instruments and Instrument Integration
• Migrate instrument software management to align with PPD IT SOPs.
• Capture and document software requirements and configurations.
• Develop validation test cases and protocols related to Instruments/Medical devices, integrations and downstream workflow validation
• Create infrastructure and data flow diagrams.
• Conduct comprehensive risk assessments.
• Collaborate with cross-functional teams including IT, QA, and lab operations.

 
Required Skills & Qualifications:

• Proven experience in Instrument/Medical device validation along with integrations and downstream workflows within a regulated (GxP) environment.
• Strong technical writing skills for documentation and test case development.
• Excellent communication skills to interact with cross-functional teams.
• Highly detail-oriented with a focus on compliance and accuracy.
• Familiarity with EMA guidelines and IT SOPs in pharmaceutical or medical device settings.
• Experience with risk assessment methodologies and validation lifecycle documentation.

 
What are the top 3 skills required for this role?
1. Instrument / Medical devices software validation
2. Instrument integration and downstream workflow validation
3. Document and validate software installed on lab instruments per EMA regulatory standards
 
Years of experience required:

• Mid to Senior Level professionals with 6–10+ years of relevant experience.
• Prior experience in lab instrumentation software validation is highly desirable.

 
 
At SPECTRAFORCE, we are committed to maintaining a workplace that ensures fair compensation and wage transparency in adherence with all applicable state and local laws. This position’s starting pay is: $ 55.00/hr.