Specialist - QA
at Julphar
Ras al-Khaimah, رأس الخيمة, United Arab Emirates -
Start Date | Expiry Date | Salary | Posted On | Experience | Skills | Telecommute | Sponsor Visa |
---|---|---|---|---|---|---|---|
Immediate | 14 Sep, 2024 | Not Specified | 18 Jun, 2024 | 2 year(s) or above | Trackwise,English | No | No |
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Description:
POSITION SUMMARY :
- In this role you will be responsible for adhering to and ensuring compliance with cGMP principles and maintain them in 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.
- Participate in Internal Audit programs.
- Preparation of Annual Product Quality Review reports.
- Responsible for Deviations and Market Complaint investigations and ensure implementation of CAPA lifecycle.
- 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.
- Maintain accurate records and perform tests on all activities conducted in the plant.
- Maintain safe and healthy work environment by following standards and procedures and complying with regulations.
- Perform Self-inspection runs in his areas.
QUALIFICATIONS, KEY EXPERIENCES / FUNCTIONAL KNOWLEDGE REQUIREMENTS:
- Bachelor’s degree in science/ pharmacy
- Minimum of 2 Years experience
- Good Computer knowledge and knowledge of QMS system “Agile, Trackwise, 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:2.0Max:7.0 year(s)
Pharmaceuticals
Production / Maintenance / Quality
Software Testing, Clinical Pharmacy
Graduate
Science pharmacy
Proficient
1
Ras al-Khaimah, United Arab Emirates