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Pharmaceutical Compliance and Quality Auditor

Active

International

Response Deadline11/30/2026, 01:00:00 PM UTC

Contract Overview

Solicitation details, issuing organization, response deadlines, documents, and interested companies for this government contract opportunity.

AI Contract Overview

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This subcontract for NHS England Project Revive seeks a Pharmaceutical Compliance and Quality Auditor to perform critical quality audits and compliance checks for prime contractors. The role involves conducting batch testing, auditing supplier manufacturing sites, and verifying certificates of analysis to ensure all operations meet MHRA standards. The successful provider must utilize laboratory testing equipment and adhere to Quality Management Systems such as ISO 9001, and the personnel performing the work must hold a valid pharmacist licensure. Key deliverables for this engagement include the production of quality assurance reports, compliance certifications, and detailed audit logs. Interested parties must respond by November 30, 2026, in accordance with the solicitation posted on November 3, 2026. The contract falls under NAICS code 541380 and is managed directly by NHS England.

General Info

Agency

NAICS

541380 - Testing Laboratories and Services

Place of Performance

GBR

Set-Aside

NONE

Documents

This scope was carved out of CM/PHG/26/5767.

The full solicitation package (2 documents), including the RFP, is on the prime solicitation, not on this scope.

View the prime solicitation

National Generic Pharmaceuticals – Project Revive

AI Contract Breakdown

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Timeline

PostedNov 3

subcontract

Response DeadlineNov 30

Submission deadline

Response Deadline

11/30/2026, 01:00:00 PM UTCin 27 days

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Organization & Contact Information

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AgencyNHS England

ContactsNo contacts available

OfficeN/A

Organization / AgencyNHS England

Office AddressN/A

ContactsNo contact information available

Full Description

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Performs quality audits and compliance checks for prime contractors on NHS England Project Revive projects. Conducts batch testing, audits supplier manufacturing sites, and verifies certificates of analysis to ensure MHRA standards. Utilizes laboratory testing equipment and Quality Management Systems such as ISO 9001. Requires pharmacist licensure. Delivers quality assurance reports, compliance certifications, and audit logs.

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