Associate Manager, Quality Compliance

Hikma Pharmaceuticals

Associate Manager for Quality Compliance at Hikma Pharmaceuticals. Ensuring compliance in the pharmaceutical manufacturing processes with international standards and regulations.

Posted 7/9/2026full-timeAmman • 🇯🇴 JordanJuniorMid-LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in auditing coordination and compliance within injectable and oral manufacturing processes, ensuring adherence to international standards and health regulations. Possesses strong problem-solving skills to investigate manufacturing issues and implement corrective actions effectively.

Highest-signal resume keywords

Auditing CoordinationInjectable Manufacturing ComplianceCAPA Plan ImplementationPharmaceutical Industry ExperienceQuality Certification (ASQ/ISO9001)

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

AuditingData IntegrityManufacturing ProcessesCorrective ActionsHealth and Safety RegulationsQuality AssuranceProcess ImprovementRegulatory ComplianceProblem InvestigationSupervisory Experience

Soft Skills

GuidanceCommunicationLeadershipCollaborationProblem-Solving

Certifications & Qualifications

B.Sc. Degree in ChemistryM.Sc. Degree in TQMQuality Certification (ASQ/ISO9001)

Industry Keywords

Pharmaceutical IndustryInjectablesOral ManufacturingContract ManufacturingLaboratory StandardsInternational StandardsCompliance AuditsCAPATQMData Integrity

About the role

Key responsibilities & impact

Providing support and guidance to the Hikma injectable sites including compounding by: Lead auditing coordination, approach, and execution for injectables/Oral/ laboratory/Data Integrity manufacturing/contract manufacturing CMOs
Ensuring internal injectable/Oral Hikma site compliance with Hikma’s rules and policies through internal audits
Following up on all observations by Hikma and third parties which includes CAPA plan implementation and ensuring timely completion.
Providing concerned Hikma employees with the required guidance related to the injectables/Oral/laboratory/Data Integrity manufacturing/contract manufacturing CMOs manufacturing processes to ensure that the related international standards and specifications are applied on all Hikma concerned processes
Investigating and studying different problems related to injectables/Oral/ laboratory/Data Integrity manufacturing/contract manufacturing CMOs manufacturing processes that might occur in all Hikma concerned functions and recommending the corrective actions accordingly
Ensuring that health and safety regulations are followed in the concerned processes to avoid accidents in the workplace during executed audits protecting the auditors

Requirements

What you’ll need

B.Sc. degree in Chemistry, Biological, Microbiology, Chemical Engineering or equivalent
M.Sc. degree in TQM or equivalent
(10) years of experience in a related position, of which at least (5) in a supervisory position
Experience in a pharmaceutical industry, Oral and Injectables manufacturing.
Quality certification on auditing e.g. ASQ/ISO9001…. etc

Benefits

Comp & perks

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