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Quality Assurance / QA Goods In - GMP / Medical

Vacancy Title: Quality Assurance / QA Goods In - GMP / Medical
Contract Type: Permanent
Location: Manchester, Greater Manchester
Industry:
Salary: Highly Competitive
Start Date: ASAP
REF: J894819_1523891788
Contact Name: Ben George
Contact Email: ben.george@russell-taylor.co.uk
Vacancy Published: 10 days ago

Vacancy 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.

Role:

  • 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.

Person:

  • 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.

Important Information: We endeavour to process your personal data in a fair and transparent manner. In applying for this role, Russell Taylor will be acting within your interest and will contact you in relation to the role, either by email, phone or text message. For more information see our Privacy Policy h t t p s : / / w w w . r u s s e l l - t a y l o r . c o . u k / p r i v a c y - p o l i c y on our website. It is important you are aware of your individual rights and the provisions the company has put in place to protect your data. If you would like further information on the policy or the GDPR please contact us on h r @ r u s s e l l - t a y l o r . c o . u k