Qualified Person

Entrust Resource Solutions

$65K — $100K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • Degree in a relevant scientific discipline or chartered status
  • Membership in the Royal Society of Chemistry, Biology, or Pharmacy
  • Certificate of Eligibility to act as a Qualified Person
  • Lead Auditor qualification (PR325 / PR330) is highly desirable
  • 3-5+ years' experience as a named QP on a manufacturing licence
  • Strong GMP background in pharmaceutical manufacturing
  • Veterinary medicinal product experience preferred, particularly in non-sterile liquids and suspensions

Responsibilities

  • Certify batches prior to release following VMR, EU GMP, and relevant Marketing Authorisations
  • Ensure compliance of manufacturing and testing activities with authorized processes
  • Review production records, deviations, and changes before certification
  • Oversee that necessary documentation and audits are completed and approved
  • Support ongoing compliance of the Quality Management System
  • Inform site leadership of issues that impact batch compliance
  • Coordinate QP activities across the team to align with production schedules

Benefits

  • High-visibility position with significant influence on site operations
  • Competitive salary range with flexibility based on experience
  • Dundee-based role in a growing, well-supported manufacturing site
Full Job Description
18th June, 2026

Qualified Person (QP) - Animal Health
📍 Dundee, Angus
💰 £65,000 - £100,000 (depending on experience)
The Role
As a Qualified Person, you will be named on the site licence and act in full compliance with the Veterinary Medicines Regulations (VMR) and Eudralex Volume 4, ensuring that all batches released meet the required standards of quality, safety and efficacy.
You will play a key role in batch certification, QMS oversight, and wider site quality leadership, working closely with operations, quality, regulatory and client teams.
Key Responsibilities
QP Certification & Compliance
  • Certify batches prior to release in line with VMR, EU GMP, Annex 16, and relevant Marketing Authorisations
  • Ensure manufacturing and testing activities comply with authorised processes and validated systems
  • Review and assess production records, deviations, changes and investigations prior to certification
  • Ensure all required documentation, audits, tests and checks are completed and approved
Quality System Oversight
  • Support ongoing compliance of the Quality Management System with legislative and regulatory requirements
  • Notify site leadership and customers of any issues impacting batch compliance
  • Maintain up-to-date knowledge of regulatory, scientific and quality management developments
Site & Team Leadership
  • Coordinate QP release activities across the QP team to support production and dispatch schedules
  • Act as Primary Deputy for the Site Quality Manager when required
  • Provide guidance and technical support on quality and compliance matters
  • Perform external audits where required
  • Liaise directly with customers on quality-related topics
About You
Qualifications
  • Degree in a relevant scientific discipline as defined under the VMR, or chartered status
  • Member of the Royal Society of Chemistry, Biology or Pharmacy
  • Certificate of Eligibility to act as a Qualified Person (permanent provisions)
  • Lead Auditor qualification (PR325 / PR330) - highly desirable
Experience
  • 3-5+ years' experience acting as a named QP on a manufacturing licence
  • Strong GMP background within pharmaceutical manufacturing
  • Veterinary medicinal product experience preferred, particularly:
    • Non-sterile liquids
    • Suspensions
  • Confident operating in a customer-facing, fast-paced manufacturing environment
Why This Role?
  • High-visibility QP position with real influence across site and customers
  • Competitive salary range with flexibility for the right experience
  • Dundee-based role within a growing and well-invested manufacturing site

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