Quality Assurance Supervisor

Grifols Egypt for Plasma Derivatives

Employer Active

Posted on 31 Mar

Experience

2 - 7 Years

Job Location

Egypt - Egypt

Education

Bachelor of Science

Nationality

Any Nationality

Gender

Not Mentioned

Vacancy

1 Vacancy

Job Description

Roles & Responsibilities

To register the Quality process as per established procedures in the electronic material management system.

To document deviations observed during the process of Quality inspection process according to GEPD company policy, and to inform stakeholders, as required.

To ensure that all tasks are performed in a timely manner.

Supervises the daily activities of the PLC Quality Assurance staff and ensures that required activities related to the receipt, storage, clearing, processing of lookback alerts, quarantine of unsuitable units, and release of source plasma for further manufacturing.

Reviews and verifies temperature documentation to ensure conformance to appropriate temperature specifications.

Investigates and documents deviations noted as a result of routine compliance reviews, internal and external audits and customer complaints.

Monitors the PLC to maintain compliance with all applicable regulations.

Trains current and new employees maintains and updates training records of the QA staff.

Supervises the activities of quality assurance staff including hiring, performance management, disciplinary action and professional development.

Desired Candidate Profile

Bachelor's degree in health-related Sciences.

Knowledge of cGMP required.

Prefer 2 years of experience in a similar position working in a Good Manufacturing Practice (GMP)-regulated environment.

Pharmaceutical background preferred.

MS Office Proficiency.

Organized and able to manage time effectively.

Ability to work within a highly regulated, labor intensive environment.

Ability to understand, explain, follow, and enforce SOPs.

Ability to plan, communicate and execute activities for the improvement of overall operations.

Strong integrity and commitment to Quality and Compliance.

Ability to work in groups and with other departments.

Excellent oral and written communication skills to produce clear and concise factual findings.

Ability to analyze and interpret data, identify problems, and propose solutions.

Effective organizational and planning skills with ability to meeting deadlines required.

Proactive and results-oriented with a strong attention to detail.

Languagesbr> Excellent written and spoken English and Arabic.

Company Industry

  • Pharma
  • Biotech
  • Clinical Research

Department / Functional Area

  • Quality
  • Testing
  • QA
  • QC
  • Inspector

Keywords

  • Quality Assurance Supervisor

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Grifols Egypt for Plasma Derivatives

https://www.careers-page.com/grifols-egypt-for-plasma-derivatives/job/7XX66VW5