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| Job Ref. ID: |
50617 |
| Job Title: |
QC Specialist |
| Division: |
QUALITY |
| Country: |
UNITED ARAB EMIRATES |
| Work Location: |
UAE (RAK head office) |
| Job Type: |
Specialist |
| Employment Type: |
Full Time Employment (Limited Contract) |
| Job Description: |
| Purpose: |
Specialist – the role holder is responsible to adhere with cGMP principles, GLP and to maintain them in effective manner.
In this role you’re responsible for analysis, investigations and update SOP. Responsible to maintain the quality of the materials, evaluate the products through internal specifications and processes. Conduct investigation to identify any inconsistencies and malfunctions. A specialist must have excellent communication skills, as well as be detail-oriented to identify areas of improvement and ensure process compliance.
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| Key responsibilities & Accountability: |
• Accountable to adhere with cGMP principles and to maintain them in effective manner
• Responsible for chemical analysis according to approved specifications, test methods and other quality procedures and perform related calculations efficiently and review quality related metrics done by analysts.
• Responsible for the follow up the correct application of test methods and ensure accuracy in implementation various procedures.
• Explains and executes the SOPs and other written procedures and ensure their right practice.
• Uses different laboratory equipment and have control over their function and cleanliness to achieve various analytical goals.
• Follows and ensures GLP, GMP and safety procedures and maintain hygienic conditions in lab.
• Prepares volumetric and/or test solutions as required through the analysis.
• Maintains records and ensure proper documentation of the analysis and enter data on SAP.
• Responsible for the release all starting materials and finished products as well as intermediate and bulk product.
• Provide support to Quality Assurance in complaint investigation.
• Responsible for updating raw material testing specification to comply with purchase requirements.
• Responsible for preparation of analytical control documents
• Responsible for the analysis of complaint samples and process validation samples
• Conduct quality control new staff training and hear/suggest feasible methods to improve efficiency and output
• Responsible to follow by literature studies the scientist development within the field of quality control
• Apart from above, the works assigned by Team Leader / Manager and support colleagues whenever necessary
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| Qualifications: |
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- Education |
• 4 years bachelor's degree in science/Pharmacy or equivalent field. |
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- Experience: |
At least 5-6 years’ experience in Quality Management in similar organization in pharma / Health care / Medical Industry.
• Strong command in English (communicating, writing and speaking) and Arabic is preferred.
• Proficient in MS Office (MS Excel and MS Word, etc.).
• Strong Knowledge in cGMP, & GDP principles.
• Must be experienced in managing complex and sensitive operational challenges. |
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- Training: |
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| Key Competencies: |
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| Technical Competencies: |
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