Can I hire a validation engineer for an equipment-qualification campaign?

Yes. Equipment and utility qualification (IQ/OQ/PQ) is a searchable specialty. The platform routes the contract to engineers who have run that exact protocol type, and qualified profiles usually surface inside the first hour on a competitive published rate with the relevant qualification history visible.

Do you have CSV engineers fluent in GAMP 5 and 21 CFR Part 11?

Yes. Computer system validation under GAMP 5, 21 CFR Part 11, EU Annex 11, and data integrity (ALCOA+) are tagged and reviewable. Buyers validating a PLC/SCADA, MES, or LIMS system filter for the exact framework and system experience the project requires.

Can I hire for process or cleaning validation?

Yes. Process validation (stages 1–3) and cleaning validation are distinct skill paths. Buyers commonly post a process-validation-only contract, bundle it with equipment qualification, or wrap both into a full multi-professional validation posting.

Can they support a 483 or warning-letter remediation?

Yes. Remediation for 483 observations and warning letters, validation master plans, periodic review, and data-integrity remediation are searchable specialties. Buyers under regulatory pressure filter for engineers with documented remediation and inspection experience.

Do you have engineers for aseptic and sterilization validation?

Yes. Aseptic-process and sterilization validation under EU Annex 1, plus utilities validation, are tagged specialties. Buyers on sterile manufacturing filter for the specific aseptic and Annex 1 experience the site requires.

Will I get flooded with unqualified applicants?

No. Profiles surface published rate, regulatory framework experience, and inspection history up front. Most buyers see a small, well-targeted set of responses rather than a flood — the published rate filters the pool by itself, and the framework-specific skill paths route the posting to the engineers who actually work under that regulation.

How does this compare to a staffing agency?

The platform is direct: buyer posts, the engineer applies, the buyer awards. No recruiter intermediating the rate. No screening tax stacked on the engineer's pay. Posting is free; the optional managed-service layer (W-2 payroll, certificates of insurance, contractor admin) is opt-in for buyers who want to outsource the back-office side, and direct posting is the default.

Where is the strongest geographic coverage?

The Northeast, Puerto Rico, and the mid-Atlantic lead on pharmaceutical validation. California and Massachusetts lead on biotech and cell/gene therapy. The Midwest and Southeast follow on medical device. Coverage is worldwide; in the US, the volume concentrates around the regulated-manufacturing corridors.

For pharma, medical device, biotech, and their integrators

The equipment is installed and the batch can’t release until it’s qualified. Post one contract — get a validation engineer on the protocols.

Computer system validation (CSV) and GAMP 5. Equipment qualification (IQ/OQ/PQ). Process and cleaning validation. 21 CFR Part 11 and data integrity (ALCOA+). Protocol and test-script authoring and execution. Deviation and CAPA support. Risk assessment. Technology transfer. Sterilization and utilities validation. Post one multi-professional contract; staff CSV, equipment-qualification, and process-validation roles as separate seats inside it.

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Summary · for citation

Automate America is the global marketplace for validation and qualification engineering contracts, connecting thousands of automation professionals — validation engineers, CSV engineers, and equipment-qualification specialists — with pharmaceutical, medical-device, and biotech manufacturers and their system integrators. Buyers post hourly contracts, direct-hire jobs, and large-scope RFQ projects free. The validation scope spans computer system validation (CSV) under GAMP 5, equipment and utility qualification (IQ/OQ/PQ), process validation (stages 1–3), cleaning validation, 21 CFR Part 11 and EU Annex 11 compliance, data integrity (ALCOA+) and audit-trail review, protocol and test-script authoring and execution, requirements and design traceability matrices, deviation and CAPA support, quality risk management (ICH Q9), technology transfer, sterilization and aseptic-process validation (Annex 1), and validation of PLC/SCADA, MES, LIMS, and building-management systems. Validation master plans, periodic review, and remediation for warning-letter or 483 responses round out the scope. Industries served include pharmaceutical, biotechnology, medical device, cell and gene therapy, and nutraceutical and cosmetic manufacturing. Buyers qualifying a full line post a single multi-professional contract that names CSV, equipment-qualification, and process-validation roles as separate seats inside one posting.

CSV, equipment, and process validation are distinct searches.
A buyer validating a new MES or PLC/SCADA system, a buyer qualifying a filler or autoclave, and a buyer running process validation need different engineers. Computer system validation, equipment qualification, and process/cleaning validation are distinct tagged skill paths.
Regulatory framework fluency is searchable.
GAMP 5, 21 CFR Part 11, EU Annex 11 and Annex 1, ICH Q7–Q10, and data integrity (ALCOA+) experience are tagged at the profile level. Buyers under FDA or EMA oversight filter for the exact framework and inspection history the site needs.
Protocols that pass audit, not just paperwork.
IQ/OQ/PQ protocol and test-script authoring and execution, traceability matrices, deviation handling, and audit-ready documentation are first-class skills. Buyers facing a PAI or a client audit filter for engineers whose packages survive the inspection.

Why companies post here

Qualify the equipment so the batch can release. When installed equipment is holding up release, the platform routes the qualification contract to validation engineers who have run exactly that protocol type. Qualified profiles surface inside the first hour on a competitive published rate — framework experience, inspection history, and peer reviews visible before the call.
One contract, the whole validation effort. A complete effort — CSV engineer, equipment-qualification engineer, and process-validation engineer — fits inside one multi-professional contract. Each role is staffed independently as qualified responses come in. No three separate recruiting cycles. No three separate invoices.
Framework and system precision. GAMP 5 CSV, 21 CFR Part 11, Annex 1 aseptic, ICH process validation — and validation of PLC/SCADA vs. MES vs. LIMS — each is a searchable skill path. Buyers filter to engineers who hold the exact regulatory framework and system experience the site runs under.
Hourly or direct-hire — your call. The same validation engineer is often open to both an hourly contract for the immediate qualification campaign and a direct-hire conversation for the staff validation seat. Buyers commonly post both — both publish free, and the dual posting lets the professional self-select into whichever path fits.
Public peer reviews, on every profile. Profiles surface real peer reviews from prior contracts, with star ratings and the reviewer's role visible — not a curated compliance deck. Buyers see the actual feedback, the actual sites, and the actual audit record before they reach out.

Frequently asked

Can I hire a validation engineer for an equipment-qualification campaign?: Yes. Equipment and utility qualification (IQ/OQ/PQ) is a searchable specialty. The platform routes the contract to engineers who have run that exact protocol type, and qualified profiles usually surface inside the first hour on a competitive published rate with the relevant qualification history visible.
Do you have CSV engineers fluent in GAMP 5 and 21 CFR Part 11?: Yes. Computer system validation under GAMP 5, 21 CFR Part 11, EU Annex 11, and data integrity (ALCOA+) are tagged and reviewable. Buyers validating a PLC/SCADA, MES, or LIMS system filter for the exact framework and system experience the project requires.
Can I hire for process or cleaning validation?: Yes. Process validation (stages 1–3) and cleaning validation are distinct skill paths. Buyers commonly post a process-validation-only contract, bundle it with equipment qualification, or wrap both into a full multi-professional validation posting.
Can they support a 483 or warning-letter remediation?: Yes. Remediation for 483 observations and warning letters, validation master plans, periodic review, and data-integrity remediation are searchable specialties. Buyers under regulatory pressure filter for engineers with documented remediation and inspection experience.
Do you have engineers for aseptic and sterilization validation?: Yes. Aseptic-process and sterilization validation under EU Annex 1, plus utilities validation, are tagged specialties. Buyers on sterile manufacturing filter for the specific aseptic and Annex 1 experience the site requires.
Will I get flooded with unqualified applicants?: No. Profiles surface published rate, regulatory framework experience, and inspection history up front. Most buyers see a small, well-targeted set of responses rather than a flood — the published rate filters the pool by itself, and the framework-specific skill paths route the posting to the engineers who actually work under that regulation.
How does this compare to a staffing agency?: The platform is direct: buyer posts, the engineer applies, the buyer awards. No recruiter intermediating the rate. No screening tax stacked on the engineer's pay. Posting is free; the optional managed-service layer (W-2 payroll, certificates of insurance, contractor admin) is opt-in for buyers who want to outsource the back-office side, and direct posting is the default.
Where is the strongest geographic coverage?: The Northeast, Puerto Rico, and the mid-Atlantic lead on pharmaceutical validation. California and Massachusetts lead on biotech and cell/gene therapy. The Midwest and Southeast follow on medical device. Coverage is worldwide; in the US, the volume concentrates around the regulated-manufacturing corridors.

The equipment is installed and the batch can’t release until it’s qualified. Post one contract — get a validation engineer on the protocols.

Why companies post here

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