Quality Assurance Supervisor

Marcyrl Pharmaceutical Industry -
Obour City, CairoPosted 6 years ago

77Applicants for5 open positions

Job Details

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Prepare and draft Quality Management System procedures for further approvals.
Supervise and authorize photocopying of controlled documents and records.
Supervise and authorize the distribution, archival, retention and destruction of controlled documents according to internal procedures.
Governance of change control process including assessment of change control, follow up and track required actions until the CCR implementation.
Governance and coordination of Quality Risk Management projects including communication of risks to concerned stakeholders follow up of effective implementation of raised action.
Handling of customer complaints which includes assessing the complaints, determine rating, coordination and facilitation of investigation report till reaching root cause and approval of corrective actions if needed.
Administer and coordinate of GMP internal audits including developing, coordination of audit schedule, identify audit team members, prepare perform and conduct audit and identifying repeated findings.
Administer and coordinate local supplier audits as a part of Suppliers Qualification Program which includes preparation of audit schedule, identify audit team members, prepare and conduct audit, review and follow up of corrective and Preventive actions sent by the supplier.
Administer and coordinate GMP training including the preparation of training calendar, ensure the execution of training sessions and review the effectiveness of training

Qualifications:

Experience:

Minimum of 5 Years relevant experience in sterile and non sterile manufacturing Compliance QA department in pharmaceutical GMP-regulated industries