A Quality Auditor is required for our manufacturing client.
The Role:
Collaborate as a solution-oriented team member to work alongside the commercial and technical operations teams, delivering QA objectives to support business growth.
* Track and report metrics and key performance indicators for the Quality Management System.
* Collaborate with stakeholders to identify and support value-added improvements and key performance indicators.
Responsibilities:
Internal Audit Program: Manage the Internal Audit program including coordinating audit schedules, reviewing findings, tracking corrective actions, and providing insights and initiatives to drive continuous improvement.
CAPA, OOS and Deviations: Review and follow-up on open actions related to Corrective and Preventative Actions (CAPA), Out of Specification (OOS) reports and Deviations.
Client Quality Audits: Support / host Client quality audits. Address findings and required actions.
Quality Training Programs: Manage quality training programs at the clients site to ensure these effectively mirror what is in place at HQ. Site lead for managing the clients SOPs and Document Control.
Site Lead Responsibilities: Document Control - Site lead for managing the clients SOPs and Document Control. Manage quality training programs at the clients site to ensure these effectively mirror what is in place at HQ.
Requirements:
* Bachelors degree in science, engineering or business preferred.
* Minimum 3 -5 years of professional experience in the pharmaceutical industry in Quality Assurance focused role.
About Us:
We are Career Wise Recruitment, specialising in recruitment of management and technical professionals for various sectors.