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Job Ref. ID:  40351 
Job Title: Non Sterile Liquids - QA Manager
Division: QA Operations
Work Location: UAE (RAK head office)
Job Type: Non Sterile Liquids QA Manager
Employment Type: Full Time Employment (Un-limited Contract)
Job Description:
Purpose: Will adhere with the cGMP principles and lead the QA operations activity for the manufacturing site with ensured compliance
Key responsibilities & Accountability: Key Responsibilities & Key Result Areas • Site GMP compliance & Audit readiness with master documents review & approvals • Leading site QA operation team • Leading team of IPC and Line Clearance • Leading team of sampling for EM, water, FG, physical samples & stability • OJT & People development • Investigations (Dev, OOSs, complaints, Recalls, etc.) • Changes assessment & Final QA approval for Implementation • CAPA effectiveness check for all site related activities • Develop and maintain continuous improvement strategy
   - Education Bachelor/Master degree in Science/Pharmacy
   - Experience: 7 years in pharmaceutical industry in QA and/or operational role for pharmaceutical non sterile manufacturing.
   - Training:
Key Competencies: • Good command in English (Communicating, writing and speaking) • Quality and Business decisions taker • KPI management • Risk Assessment knowledge • Problem Solving & Strategic Agility • Team building and structure & Had a proved experience of leading people with different knowledge and levels • Developing Direct Reports • Departmental budgeting and basic finance knowledge • Knowledgeable with Pharmaceutical cGMP guidelines • Had a proved experience in quality documents issuance and review (SOP, Protocols, Assessments, etc.) • Had a proved experience of managing QIPs as well as leading the continuous improvements • Ability to define the business and quality priorities • Had a proved experience of projects management from quality perspective • Proved experience in culture change contribution • SAP experience  
Technical Competencies:  


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