Purpose:
Will adhere with the cGMP principles and perform In-process Quality checks in Shop floor
Key responsibilities & Accountability
1. Performs in-process quality checks in manufacturing and/or packaging area (Tablets/Capsules/liquids/Semi solids/Injectables) and captures test results in batch records.
2. Performs a quality review of log books.
3. Performs Line clearance activities
4. Participate in Internal and External Audit program’s
5. Ensure the in-process check equipment’s are adequately calibrated and functions properly.
6. Compliance to current Good Manufacturing Practices (cGMP) and Good Distribution Practices (GDP).
7. Assists in preparation of Annual Product Quality Review reports.
Qualifications:
- Education Bachelor/Master degree in Science/Pharmacy
- Experience 1-3 years in pharmaceutical industry preferably in onsite inspection
Experience in the companies having GMP approval from USFDA/MHRA/TGA/ANVISA/EU authorities.
Flexible to work in all Shifts and not sensitive to B-Lactams
Key Competencies: Strong written and verbal communication skills for English language. Basic IT skills and knowledge in Microsoft office (word, excel, etc.) Honesty & Integrity Self-confident.
Technical Competencies Knowledgeable with all SOPs, GMP, MFM, and SAP………..
*** تقدم على الرابط التالي : Apply on the following link ***
https://www.naukrigulf.com/qa-junior-specialist-jobs-in-uae-in-julphar-gulf-pharmaceutical-industries-1-to-3-years-jid-231219000043
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