Mid Level Validation Consultant Jobs
Mid level validation consultant jobs go to professionals ready to own validation projects end to end, guide junior team members, and make technical decisions with minimal oversight. Roles are predominantly on-site and hybrid across Technology & Software, Consulting & Professional Services, and Electronics & Hardware, with Katalyst Healthcares & Life Sciences, United Pharma, and Veeva Systems actively hiring at this level now.
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Showing 5 of 97+ Mid Level Validation Consultant jobs
INTRODUCTION
The Automation Validation Engineer is responsible for execution of validation and commissioning protocols for automated process control systems. The position requires in-depth knowledge of automation validation, fill and finish lines, general equipment knowledge, cGMP, and GDP. This position is 100% onsite with no remote work in the Boston area.
ROLE AND RESPONSIBILITIES
- Perform and support execution of validation protocols/projects
- Develop, review, and redline URS/FRS/DDS
- Support change management process
- Support project level customer communications and coordination efforts
- Prepare and execute commissioning documents
- Prepare and execute IOQ documents and summary reports
- Maintain project lifecycle documentation in accordance with Mangan Biopharm internal procedures and client procedures
BASIC QUALIFICATIONS
- Bachelor's degree in engineering, science, or related field with at least 4 years of experience
- Master's degree in engineering, science, or related field with 3 years of experience in Biotechnology or Pharmaceutical GMP environment
PREFERRED QUALIFICATIONS
- Experience with Biopharma manufacturing equipment specifically: fermenter, centrifuge, harvest filter skid, ultrafiltration skid, homogenizer, clean in place (CIP), utilities (WFI, Clean Steam, Compressed Air)
- The Validation engineer must work with automation, APO, and Quality team closely
- Experience in GAMP is preferred
- Excellent organizational and communication/people skills
Skills
- allen bradley
- automator
- cgmp
- commissioning
- compactlogix
- configurator
- gdp
- hmi
- ifix
- read tape measure
- risk assessment
- scada
- validation
Top Skills Details
- allen bradley
- automator
- cgmp
- commissioning
- compactlogix
- configurator
- gdp
- hmi
- ifix
- read tape measure
- risk assessment
- scada
- validation
INTRODUCTION
The Automation Validation Engineer is responsible for execution of validation and commissioning protocols for automated process control systems. The position requires in-depth knowledge of automation validation, fill and finish lines, general equipment knowledge, cGMP, and GDP. This position is 100% onsite with no remote work in the Boston area.
ROLE AND RESPONSIBILITIES
- Perform and support execution of validation protocols/projects
- Develop, review, and redline URS/FRS/DDS
- Support change management process
- Support project level customer communications and coordination efforts
- Prepare and execute commissioning documents
- Prepare and execute IOQ documents and summary reports
- Maintain project lifecycle documentation in accordance with Mangan Biopharm internal procedures and client procedures
BASIC QUALIFICATIONS
- Bachelor's degree in engineering, science, or related field with at least 4 years of experience
- Master's degree in engineering, science, or related field with 3 years of experience in Biotechnology or Pharmaceutical GMP environment
PREFERRED QUALIFICATIONS
- Experience with Biopharma manufacturing equipment specifically: fermenter, centrifuge, harvest filter skid, ultrafiltration skid, homogenizer, clean in place (CIP), utilities (WFI, Clean Steam, Compressed Air)
- The Validation engineer must work with automation, APO, and Quality team closely
- Experience in GAMP is preferred
- Excellent organizational and communication/people skills
Skills
- allen bradley
- automator
- cgmp
- commissioning
- compactlogix
- configurator
- gdp
- hmi
- ifix
- read tape measure
- risk assessment
- scada
- validation
Top Skills Details
- allen bradley
- automator
- cgmp
- commissioning
- compactlogix
- configurator
- gdp
- hmi
- ifix
- read tape measure
- risk assessment
- scada
- validation
See All 97 Mid Level Validation Consultant Jobs
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Find JobsMid Level Validation Consultant Job Market
Who's Hiring
- Katalyst Healthcares & Life Sciences16
- United Pharma10
- Veeva Systems6
- CAI4
- Wipro4
Top Industries Hiring
- Technology & Software29
- Consulting & Professional Services28
- Electronics & Hardware8
- Biotechnology & Pharmaceuticals4
- Automotive3
Mid Level Validation Consultant Jobs: Frequently Asked Questions
How do I get a mid level validation consultant job?
Position your experience around ownership, not just participation. Highlight validation protocols you authored, deviations you resolved independently, and cross-functional projects you led rather than supported. Tailor your resume to show progression in scope and responsibility. Mid level roles reward candidates who can demonstrate they have moved from executing tasks to driving validation strategy with limited direction from management.
Which companies hire mid level validation consultants?
Companies hiring mid level validation consultants right now include Katalyst Healthcares & Life Sciences, United Pharma, and Veeva Systems, based on current listings on Migrate Mate as of November 2026. At this level, hiring comes from both large regulated manufacturers and specialized consulting firms that staff validation projects on a contract or permanent basis.
Are there remote mid level validation consultant jobs?
Yes, though the role is more on-site than most. About 25% of mid level validation consultant openings are remote or hybrid as of November 2026, with fully remote positions typically limited to documentation-heavy or protocol-writing phases of a project rather than hands-on equipment qualification work.
How do I move up to a mid level validation consultant role?
The path from entry to mid level runs through demonstrated ownership. Early-career validation professionals build toward mid level by taking on full validation lifecycle projects, documenting measurable outcomes like reduced deviation rates or faster qualification timelines, and developing fluency in regulatory frameworks like FDA 21 CFR Part 11 or EU Annex 11. Consistent delivery without close supervision is what signals readiness.
Which industries hire the most mid level validation consultants?
Mid Level validation consultant roles concentrate in Technology & Software, Consulting & Professional Services, and Electronics & Hardware, based on current listings on Migrate Mate as of November 2026. These sectors drive hiring at this level because their regulatory obligations require ongoing validation of equipment, software, and processes, creating steady demand for professionals who can operate independently on complex compliance programs.