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Manager,Quality Control

Cairo, Egypt
Posted 5 years ago
125Applicants for4 open positions
  • 6Viewed
  • 0In Consideration
  • 0Not Selected
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Job Details

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Job Description

Essential Duties and Responsibilities:

  • Managing that appropriate tests are performed up to standards on all drug components (Intermediates and Finished Products) in order to ensure quality of starting materials entering marcyrl products
  • Reviewing the analytical reports written by analysts & checked by supervisors/Section head "released on the Oracle system ERP" to ensure quality of final product
  • Deciding final disposition whether approved, rejected & reworked of Raw Materials, Packaging Materials & Intermediates after reviewing of analytical reports
  • Auditing all specs. & general compendium with sections heads & request needed ones to ensure that all tests are performed according to latest approved guidelines
  • Checking & Approving Certificates of analysis for all products to MOH in cooperation with QA responsible to get local regulatory approval on Marcyrl produced batches
  • Securing that routine testing of water system takes place according to schedule, review & approve certificates of analysis to ensure the quality of purified water as considered a starting material.
  • Controlling & Maintaining the product stability process schedule "Long term & Ongoing" in cooperation with the stability process team to ensure product quality throughout whole shelf-life.
  • Enclosing the product complaint which require chemical analysis by QC analyst to be documented & fully investigated the case of customer complaints and avoid reoccurrence
  • Preparing & Monitoring QC budget and CapEX plan in order to ensure continuous adherence to annual budget.
  • Revising & Approving the requirements of QC supplies, reference and working standards, Chemicals, spare parts as well as glassware & stationary to sustain QC budget and ensure continuous fulfilling of customers needs
  • Preparing a purchasing report of any required QC equipment & accessories clarifying exact URS to get Top management approval. This is to match upgraded techniques.
  • Technical Interviewing for QC candidates to select the most suitable calibers to fulfill the positions and thus impact upon the department productivity
  • Scheduling, Assigning & Supervising the work of the subordinates in the dept. to ensure meeting of customer needs and availability during overtime hours & weekend when necessary "according to production activities"
  • Mastering the QC technical training efficiently in accordance with assigned role requirements to match company objectivesny QC member compliant "in coordination with HR department" in order to improve the working atmosphere.
  • Evaluating the subordinates' performance by discussing the appraisal to ensure team performance maximization and to match agreed commitment.
  • Identifying operational risk at QC, hosting audits, change controls and representing QC in management review
  • Reporting frequently to General manager to highlight the progress of QC. for continuous alignment with top management and company goals.
  • Coordinating with production & validations to begin validation of process according to time schedule to comply with QA validation requirements.

Job Requirements

  • General: - B.Sc of pharmaceutical Science

Technical:-

  • 12-15 experience in Quality Control
  • M.P training course
  • Good command of English
  • Computer skills
  • Advanced Decision Making Skill
  • Proven Attention to Details Skill
  • Excellent Time Management Skill
  • Dynamic Problem Solving Skill
  • Very good Written Communication Skill
  • Professional Stewardship of Resources Skill
  • Excellent Team Management Skill
  • Good Developing Others Skill
  • Highly Networking & Relationship building Skill

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