Quality Assurance / QA Goods In - GMP / Medical

Job Title: Quality Assurance / QA Goods In - GMP / Medical
Contract Type: Permanent
Location: Manchester, Greater Manchester
Salary: Highly Competitive
Start Date: ASAP
Reference: J894819_1523891788
Contact Name: Ben George
Contact Email:
Job Published: April 16, 2018 16:16

Job Description

Role: Quality Assurance / QA Specialist - Goods In / External Audits

Location: Manchester, North West UK - Permanent

Salary: Highly Competitive + Great Benefits

Russell Taylor Group has a fantastic opportunity for a Quality Assurance / QA Specialist to join a Global Medical Device ISO 13485 that specialises or has experienced of Goods In / External Auditing experience. If you are looking for a full time permanent role and the opportunity to work for a Global Medical Device company who really make a difference within the healthcare industry, who also offer excellent benefits please apply within.


  • You will be responsible for the release of raw materials used in the Manufacturing Process ( GMP )and in accordance to our clients Quality Management System ( QMS )
  • You will perform QA / QC checks on all raw materials entering the warehouse and complete all necessary quality documentation.
  • Release of raw materials as delegated for the manufacturing department.
  • Client engagement to resolve supplier quality issues raising NCE records.
  • Support activities associated with aspects of the Quality Management System ( QMS )in relation to raw materials; CAPA, Non Conformances, Extension Requests, Material Review Board ( MRB ), Supplier Quality Management.
  • Attends regular meetings as required for updates on Quality issues and material products awaiting Goods in inspections.
  • Develop / Revise SOPS and assist in the development of continuous improvement of the QMS / Quality Management System.


  • Must have "Goods In" Quality checking / QA / QC experience.
  • Worked within a Manufacturing environment would be an advantage, GMP, however will consider other candidates from a highly regulated environment.
  • Must have a working knowledge of QMS / Quality Management System and ISO standards; such as ISO 17025 or ISO 13485.
  • High attention to detail, ERP IT CRM experience, SAP / Oracle highly advantageous.
  • At least 2 + years experience working within a QA Role, with Goods in experience.

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