Jr. Specialist - QA (Sterile)
at Julphar
Ras al-Khaimah, رأس الخيمة, United Arab Emirates -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 17 Sep, 2024 | Not Specified | 18 Jun, 2024 | 3 year(s) or above | English | No | No |
Required Visa Status:
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US Citizen | Student Visa |
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Employment Type:
Full Time | Part Time |
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Contract to Hire – Corp 2 Corp |
Description:
POSITION SUMMARY :
- In this role you will be responsible for adhering to and ensuring compliance with cGMP principles and maintaining them in an effective manner.
- Perform in-process quality check activities according to SOP in production / packaging departments (Tablets/Capsules/liquids/Semi solids/Injectable) in complying with cGMP principles and captures test results in batch records.
- Check the required tests for all products during production / packaging process.
- Inspect and check incoming materials by confirming specifications and return unacceptable materials.
- Revise all documents for in process control and perform a quality review of logbooks.
- Responsible to revise and document for inspection results and complete all required documents for in process control by completing reports and logs, summarizes re-work and waste, and inputs data into quality database on SAP system.
- Ensure the in-process check equipment’s are adequately calibrated and functions properly.
- Perform and check the line before start (production/packaging) and give the clearance for the work.
- Perform Initial investigations for reported incidents and deviation in the respected site
- Participate in the preparations of APQRs of the respected site.
- Maintain safe and healthy work environment by following standards and procedures and complying with regulations.
QUALIFICATIONS, KEY EXPERIENCES / FUNCTIONAL KNOWLEDGE REQUIREMENTS:
- Bachelor of degree in pharmacy/Science
- Minimum 0 to 3 years in quality operation in Sterile manufacturing
- Knowledge of QMS system “Agile, Track wise, Ampelogic”
- Proficient in English.
- Quality and Business decisions taker
- Good Knowledge and command on cGMP
- Risk Assessment knowledge
Responsibilities:
Please refer the Job description for details
REQUIREMENT SUMMARY
Min:3.0Max:8.0 year(s)
Pharmaceuticals
Production / Maintenance / Quality
Clinical Pharmacy
Graduate
Proficient
1
Ras al-Khaimah, United Arab Emirates