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Sr. Officer, QA at Hikma Pharmaceuticals PLC

Al Salt, Balqa, Jordan -

Full Time

Start Date

Immediate

Expiry Date

10 Oct, 26

Salary

0.0

Posted On

12 Jul, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Veeva, Analytical Testing, Data Analysis, Data Integrity, LIMS, Laboratory Instrumentation, GMP, SOPs, Deviations, Investigations, Quality Auditing, Quality Control, CAPA, Change Control, Technical Writing, Validation

Industry

Description

Sr. Officer – QA position, Job Responsibilities: Handle and approve deviations, investigations, and laboratory investigations. Ensure product compliance with specifications and cGMP requirements. Approve validation protocols/reports, process validation, stability protocols, APRs, and master batch records. Review and approve change controls. Perform risk assessments and review gap analysis reports. Conduct QA rounds, and in-process checks, documentation reviews, ensuring completeness and compliance. Create, update, and review SOPs, including periodic review cycles. Prepare and review CAPA and quarterly reports, ensuring effectiveness tracking. Issue and follow up on Quality Circles. Performs line clearance and area verification Monitors GMP compliance on the shop floor Reviews and approves batch manufacturing records (BMRs) Reviews equipment logs, cleaning logs, yield calculations Verifies sampling, dispensing, packaging activities Issues and receives labels, controlled documents Qualifications: Bachelor’s degree with minimum 4 years of relevant work experience very good experience in deviations and investigations. Specialized Skills: Veeva, Analytical Testing, Data Analysis, Data Integrity, LIMS, Laboratory Instrumentation GMP, SOPs, Safety Awareness Deviations, Investigations, Quality Auditing, Quality Control, CAPA, Change Control, Technical Writing, Validation Behavioral Competencies: Collaboration & Teamwork, Initiative & Drive for Results, Resilience & Adaptability, Change & Innovation, Problem Solving & Decision Making

Responsibilities

Oversee quality assurance by managing deviations, investigations, and change controls to ensure product compliance with cGMP requirements. Perform shop floor monitoring, line clearances, and review batch manufacturing records and validation protocols.