QAO Sterile Value Stream Manager

Julphar
United Arab Emirates
Workplace: OnsiteFull timeFunction: Administration & Executive AssistanceExperience: 10+ yearsEducation: bachelorsSkills: ["Quality oversight","Leadership","Accountability","Risk assessment","Training"]

Lead end-to-end Quality Assurance oversight for sterile pharmaceutical manufacturing, including batch certification and release, QMS compliance, investigations, CAPA, validation, and product lifecycle management. Act as the site’s Qualified Person (QP), ensure cGMP and GMP documentation practices are followed, approve deviations, CAPAs, and change controls, and drive quality culture through inspections, KPI reporting, and training across cross-functional teams.

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Julphar
Julphar
3 hours ago

QAO Sterile Value Stream Manager

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Last checked: 3 hours agoStatus: Live

Job Summary

Lead end-to-end Quality Assurance oversight for sterile pharmaceutical manufacturing, including batch certification and release, QMS compliance, investigations, CAPA, validation, and product lifecycle management. Act as the site’s Qualified Person (QP), ensure cGMP and GMP documentation practices are followed, approve deviations, CAPAs, and change controls, and drive quality culture through inspections, KPI reporting, and training across cross-functional teams.
Location: United Arab Emirates
Workplace: Onsite
Employment Type: Full time
Job Function: Administration & Executive Assistance
Seniority: Manager level

Key Responsibilities

  • •Lead end-to-end QA oversight for sterile pharmaceutical manufacturing, acting as the Qualified Person (QP) for batch certification and release.
  • •Ensure cGMP compliance across manufacturing plants through review of documentation, environmental conditions, gowning/cleanliness, and equipment qualification/calibration status.
  • •Review and approve deviations investigations and product quality investigations, ensuring timely completion and assessments; approve CAPA and change control.
  • •Oversee product lifecycle management activities including technology transfer, process validation (PPQ), commercial manufacturing, continued process verification (CPV), and product discontinuation.
  • •Manage QA operations KPI adherence, coordinate quality improvement and quality culture with cross-functional teams, and provide training and successor development for QA batch release and compliance processes.

Key Requirements

  • •Bachelor of Pharmacy with minimum 10+ years of experience in Quality Assurance oversight of sterile manufacturing operations.
  • •Experience with batch release and product lifecycle management.
  • •Strong knowledge and command of QMS and cGXP systems.
  • •Experience with risk assessment, including lifecycle risk assessments.
  • •Good GMP knowledge and familiarity with QMS compliance activities such as documentation, investigations, and CAPA.
Experience:10+ yearsSterile manufacturingPharmaceutical manufacturingQuality assuranceQMSCGMP
Education:Bachelor's
Skills:Quality oversightLeadershipAccountabilityRisk assessmentTraining
Tech Stack:QMSCGMPCGXPCAPABatch releaseAPQRPQRCPVPPQ

Company Brief

Julphar
Gulf Pharmaceutical Industries, known as Julphar, develops and manufactures a broad range of pharmaceutical products, including generics and healthcare solutions. It serves markets across the Middle East and internationally from its UAE base.
Industry: Pharmaceuticals
Company Size: Enterprise (1,001+ employees)
Growth: Public Company
Valuation: Public Company (Market Cap in USD)
Funding: IPO / Publicly Listed
Headquarters: Ras Al Khaimah, United Arab Emirates
Founded: 1980
WebsiteLinkedIn