Senior Instrument Software Validation Engineer

TechDigital Group

North Carolina

Hybrid

USD 90,000 - 150,000

Full time

14 days+

Get more replies from employers

Send a job-specific resume in minutes.

Job summary

TechDigital Group seeks an experienced Senior Instrument/Medical Device Validation specialist to lead validation efforts for lab instruments and integrations in a GMP/GxP setting.

You will document requirements, develop test protocols, and ensure alignment with EMA guidelines and IT SOPs, collaborating with IT, QA, and lab operations across cross-functional teams in North Carolina. This role offers growth in a regulated environment with impactful projects.

Qualifications

  • Proven experience in Instrument/Medical device validation within a regulated (GxP) environment.
  • Strong technical writing for documentation and test case development.
  • Excellent cross-functional communication with IT, QA, and lab operations.
  • Familiarity with EMA guidelines and IT SOPs in pharma or medical devices.

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.

Skills

Instrument/Medical device validation
Instrument integration
Downstream workflow validation
Technical writing

Job description

TechDigital Group seeks an experienced Senior Instrument/Medical Device Validation specialist to lead validation efforts for lab instruments and integrations in a GMP/GxP setting.

You will document requirements, develop test protocols, and ensure alignment with EMA guidelines and IT SOPs, collaborating with IT, QA, and lab operations across cross-functional teams in North Carolina. This role offers growth in a regulated environment with impactful projects.

Get your free, confidential resume review.
or drag and drop your file here.
Similar jobs

Similar jobs worth comparing

Senior Validation Specialist - Pharma/Medical Devices
Senior Validation Specialist - Pharma/Medical Devices

Integration International Inc. • Marion (NC)

On-site
Instrument Software validation Engineer
Instrument Software validation Engineer

TechDigital Group • North Carolina

Hybrid
USD 90,000 - 150,000
Instrumentation Software Validation Analyst
Instrumentation Software Validation Analyst

Katalyst CRO • Cincinnati (OH)

On-site
USD 90,000 - 120,000
Senior Validation Engineer Medical Devices GMP Expert
Senior Validation Engineer Medical Devices GMP Expert

Medline • Shanghai (VA)

On-site
USD 110,000 - 160,000
Health insurance
Life and disability
401(k) contributions
+1
Senior Lab Instrument Validation Lead – GxP
Senior Lab Instrument Validation Lead – GxP

Compunnel, Inc. • Highland Heights (KY)

On-site
USD 90,000 - 120,000
Equipment Engineer
Equipment Engineer

United Pharma Technologies Inc • New York (NY)

On-site
USD 85,000 - 110,000
Senior Quality Engineer, Medical Devices & Validation
Senior Quality Engineer, Medical Devices & Validation

TechDigital Group • Cincinnati (OH)

On-site
USD 85,000 - 120,000
Senior Lab Instruments Software Validation Analyst / Technical Writers
Senior Lab Instruments Software Validation Analyst / Technical Writers

Compunnel, Inc. • Highland Heights (KY)

On-site
USD 90,000 - 120,000
Validation Specialist
Validation Specialist

United Pharma Technologies Inc • Massachusetts

On-site
USD 90,000 - 120,000
Validation Engineer: Medical Devices & GMP Compliance
Validation Engineer: Medical Devices & GMP Compliance

Veg Group • Aibonito (PR)

On-site
USD 85,000 - 120,000