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QA Compliance officer

Wiltshire   •  Negotiable  •  Permanent, Full time


MAIN DUTIES AND RESPONSIBILITIES

QA Compliance Officer, supported by the Senior Compliance Officer, will be responsible for:

Ensuring all work complies with guidance set forth in EU and US FDA GMP regulations governing the manufacture, storage and distribution of medicinal products;

Internal and external (supplier) audits including organising, planning, performing, reporting and review of evidence;

Raising, investigating and closing out CAPAs;

Ensuring supplier questionnaires are satisfactorily completed on time by key manufacturers and suppliers;

Liaising with suppliers to obtain relevant information for their approval to provide key materials and services to the company;

Approval of GMP monographs;

Producing technical agreements for the supply of goods and services from critical suppliers;

Initiate and progress supplier complaints;

Maintain the supplier monitoring database and associated spreadsheets for tracking;

Assisting QA overview of manufacturing and testing areas;

Providing input to KPI reports for the team;

Undertaking relevant training

Undertaking work in accordance with the company health and safety policies and procedures.

  • Agency: Cpl Life Sciences
  • Contact: Sheldon Grant
  • Reference: JO-2109-475712
  • Posted: 6th September 2021
  • Expires: 4th October 2021

Cpl Life Sciences

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