Quality Assurance Specialist

Quanta Consultancy Services Ltd; United Kingdom; Remote; GBP 40,000 - 60,000; Full time

Job summary

A leading pharmaceutical consultancy in the UK is seeking a Quality Assurance Specialist for a 6-month remote contract. The role involves evaluating products, managing deviations, and ensuring compliance with regulations. Candidates should have experience in pharmaceutical manufacturing, especially with biologics and vaccines. This opportunity offers a chance to contribute to significant pharmaceutical projects.

Qualifications

• Experience with manufacturing operations and/or analytical expertise associated with biologics and/or vaccines.
• Competency in Analytical Method Validation/Verification/Transfer.
• Experience with qualification of manufacturing facilities/equipment.

Responsibilities

• Evaluate and/or release products to ensure compliance with policies.
• Review and approve change controls.
• Manage deviations and complaints; assist in significant investigations.

Skills

Aseptic manufacturing experience

Quality Risk Management (QRM)

Analytical Method Validation/Verification/Transfer

Job description

Quality Assurance Specialist - Remote Working - 6 Month Contract

Do you want to be involved with exciting pharmaceutical projects?

When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are looking to add to their team and require a Quality Assurance Specialist for a 6 months maternity cover.

Essential Duties and Responsibilities for this role include, but are not limited to, the following:

• Evaluate and/or release products to other sites and/or to the market with the assurance that the goods were produced in conformance to all applicable policies/procedures and compliance with all governing regulations
• Review and approve change controls
• Manage routine and complex deviations and complaints and assist in the coordination of significant investigations
• Conduct routine and solve complex analytical change requests and support process modification change controls
• Stability Program management, including review of stability reports, and Annual Product Review assembly
• Provide on-site guidance in the preparation of metrics, procedures, and guidelines
• Track and monitor operational and quality performance of the EP/ExP and can work with supplier to develop Corrective and preventive action (CAPA) plans
• Assist the maintenance of retention samples, ship reagents and samples to support licensure and foreign registration
• Responsible for shipment under quarantine
• Support routine process validation; review and approve validation reports/tech transfer
• Prepare pre-PAI assessments, support document requests for regulatory filings and post approval changes

Desirable Experience:

• Experience with manufacturing operations and/or analytical expertise associated with biologics and/or vaccines. Aseptic manufacturing experience
• Experience with qualification of manufacturing facilities/equipment (i.e. Process/Cleaning Validation, IQ/OQ/PQ)
• Competency in Analytical Method Validation/Verification/Transfer and Analytical Standards
• Quality Risk Management (QRM) Experience

If this role is of interest to you, please apply now!

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