Manager- Quality OSD Value Stream (Ras Al khaima, United Arab Emirates)

Julphar
United Arab Emirates
Workplace: OnsiteFull timeFunction: Quality & Regulatory (Non-Software)Experience: 10+ yearsEducation: bachelorsSkills: ["Accountability","Team-building","Time management","Communication","Root cause analysis"]

Lead end-to-end Quality Assurance for pharmaceutical manufacturing sites, serving as the Qualified Person (QP) for batch certification and release. Ensure cGMP compliance across documentation, gowning, cleanliness, environmental conditions, equipment qualification, and SOP adherence. Oversee deviations, investigations, CAPA, and change control in Ample Logic, manage product lifecycle activities (tech transfer, PPQ, CPV, stability, discontinuation), and drive quality culture, audits, KPIs, and team training.

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Julphar
Julphar
2 days ago

Manager- Quality OSD Value Stream (Ras Al khaima, United Arab Emirates)

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Source: Company careers pageValidated by: Fursa AI
Last checked: 12 hours agoStatus: Live

Job Summary

Lead end-to-end Quality Assurance for pharmaceutical manufacturing sites, serving as the Qualified Person (QP) for batch certification and release. Ensure cGMP compliance across documentation, gowning, cleanliness, environmental conditions, equipment qualification, and SOP adherence. Oversee deviations, investigations, CAPA, and change control in Ample Logic, manage product lifecycle activities (tech transfer, PPQ, CPV, stability, discontinuation), and drive quality culture, audits, KPIs, and team training.
Location: United Arab Emirates
Workplace: Onsite
Employment Type: Full time
Job Function: Quality & Regulatory (Non-Software)
Seniority: Manager level

Key Responsibilities

  • •Provide end-to-end Quality Assurance oversight across pharmaceutical manufacturing sites and act as Qualified Person (QP) for batch certification and release.
  • •Ensure cGMP compliance by monitoring documentation practices, batch record accuracy, cleanliness, environmental conditions, calibrated/qualified equipment, and adherence to SOPs and instructions.
  • •Review and approve deviation investigations, complaints, recalls, CAPA, and change controls; ensure timely completion in Ample Logic.
  • •Lead product lifecycle management (technology transfer, process validation/PPQ, commercial manufacturing, CPV, product discontinuation) including stability programs and lifecycle risk assessments.
  • •Perform site inspections, support audit readiness for internal/external audits, lead batch document audits and retention sample checking, supervise shipment checks before dispatch, and develop/train successors and the QA team.

Key Requirements

  • •Bachelor of Pharmacy.
  • •Minimum 10+ years of experience in Quality Assurance oversight of Oral Solid Dosage (OSD) manufacturing operations.
  • •Demonstrated batch release experience and product lifecycle management experience.
  • •Good experience with QMS systems and strong knowledge of cGXP and risk assessment.
  • •Excellent oral and written communication skills in English, with strong time and task management and accountability.
Experience:10+ yearsPharmaceutical manufacturingOral solid dosage (OSD)
Education:Bachelor's in Pharmacy
Skills:AccountabilityTeam-buildingTime managementCommunicationRoot cause analysis
Languages:English
Tech Stack:CGMPAmple LogicQMSCGXPBMRBPRPPQCPVAPQRPQR

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