Quality Advisor

Talentmark

Liverpool

Hybrid

GBP 39,950 - 50,971

Full time

14 days+

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Job summary

Talentmark is recruiting a Quality Advisor on a 6‑month contract for a role blending site and home working in Speke. You will ensure supplier compliance and support GMP‑driven QA activities across external partners and product launches.

The position requires a scientific degree or equivalent experience, strong regulatory knowledge, and hands-on QA experience in medicinal goods under GMP. DBS may be required.

Qualifications

  • Experience in QA or pharmaceutical production under GMP.
  • Knowledge of regulatory requirements and global QA operations.
  • Ability to assess supplier performance and approve third-party onboarding.

Responsibilities

  • Work with external suppliers to ensure compliance with requirements.
  • Support qualification and validation activities at third parties and product launches.
  • Manage change control activities internally and externally.
  • Evaluate supplier Product Quality Reviews.
  • Monitor KPIs for supplier/contract manufacturers to detect issues.

Skills

Regulatory knowledge
Quality Assurance
GMP compliance
Supplier management
Pharmaceutical QA

Education

Scientific degree

Job description

Talentmark are recruiting for a Quality Advisor to join a company in the animal health and pharmaceutical industry on a contract basis for 6 months. This is a hybrid role with 3 days per week at the client's site in Speke and 2 days working from home.

Salary: From £29.23 per hour to £37 per hour depending on experience.

Quality Advisor Role:
  • Work with external suppliers to ensure they are effective and compliant with requirements.
  • Assure the robust selection and on-boarding of Third Parties in compliance with regulatory and GMP standards.
  • Support and provide Quality input for qualification and validation activities at Third Parties and product launches.
  • Manage and support change control activities both internally and externally.
  • Evaluate supplier Product Quality Reviews.
  • Monitor Supplier/Contract Manufacturer or third party KQI’s to proactively detect compliance issues.
Your Background:
  • Hold a relevant scientific degree or have equivalent working experience.
  • Thorough knowledge and understanding of Regulatory requirements.
  • Experience in Quality Assurance or Pharmaceutical Production of Medicinal goods under GMP requirements.
  • Working experience within global QA operations.
Company:

Our client specialises in animal health. They advance their vision of food and companionship, enriching life by developing innovative solutions that protect and enhance animal health.

Apply:

For more information, or to apply for this Quality Advisor, please contact the Key Accounts Team on (phone number removed) or email (url removed). Please quote reference (Apply online only).

It is essential that applicants hold entitlement to work in the UK.

Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

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