Specialist - QA (Sterile)

✓ Verified Job

Canonical indexed version, validated from employer's careers page.

Source: Company careers pageValidated by: Fursa AI

Last checked: 22 hours agoStatus: Live

Job Summary

Perform line clearance and release activities and conduct in-process quality checks for products during manufacturing and packaging. Maintain complete traceability by documenting test results and observations in batch-related records, while ensuring proper materials and components are used. Ensure compliance with cGMP, support audits and audit readiness, manage QMS deviations, complaints, CAPA, and change control within the Ampelogic system, and assist with APQR preparation.

Location: United Arab Emirates

Workplace: Onsite

Employment Type: Full time

Job Function: QA, Test & Release Engineering

Seniority: Mid level

Key Responsibilities

•Perform line clearance and release activities according to SOPs.
•Conduct in-process quality checks during manufacturing and packaging, ensuring results meet defined limits and timelines.
•Accurately document test results and observations in batch-related documentation for traceability and compliance.
•Maintain cGMP adherence in the assigned area, including verification of documentation, record integrity, and gowning/cleanliness.
•Handle QA activities such as audit participation, QMS deviations and market complaints, CAPA and change control in Ampelogic, and support APQR preparation.

Key Requirements

•Bachelor of Pharmacy.
•4 years of experience in Quality assurance.
•Knowledge of computer systems and MS Office.
•Good knowledge of SOPs and batch records review.
•Advanced knowledge of cGMP principles and the production process.

Experience:4+ yearsQuality assurancePharmaceutical manufacturing

Education:Bachelor's in Pharmacy

Skills:Attention to detailDocumentationQuality focus

Tech Stack:MS OfficeSOPsBMRBPRMPIMIVAPQRQMSCAPAChange controlAmpelogic

Company Brief

Julphar

Website

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Julphar

2 days ago

Specialist - QA (Sterile)

✓ Verified Job

Canonical indexed version, validated from employer's careers page.

Source: Company careers pageValidated by: Fursa AI

Last checked: 22 hours agoStatus: Live

Job Summary

Location: United Arab Emirates

Workplace: Onsite

Employment Type: Full time

Job Function: QA, Test & Release Engineering

Seniority: Mid level

Key Responsibilities

•Perform line clearance and release activities according to SOPs.
•Conduct in-process quality checks during manufacturing and packaging, ensuring results meet defined limits and timelines.
•Accurately document test results and observations in batch-related documentation for traceability and compliance.
•Maintain cGMP adherence in the assigned area, including verification of documentation, record integrity, and gowning/cleanliness.
•Handle QA activities such as audit participation, QMS deviations and market complaints, CAPA and change control in Ampelogic, and support APQR preparation.

Key Requirements

•Bachelor of Pharmacy.
•4 years of experience in Quality assurance.
•Knowledge of computer systems and MS Office.
•Good knowledge of SOPs and batch records review.
•Advanced knowledge of cGMP principles and the production process.

Experience:4+ yearsQuality assurancePharmaceutical manufacturing

Education:Bachelor's in Pharmacy

Skills:Attention to detailDocumentationQuality focus

Tech Stack:MS OfficeSOPsBMRBPRMPIMIVAPQRQMSCAPAChange controlAmpelogic

Company Brief

Julphar

Website