Jr. Specialist- QC

Julphar
United Arab Emirates
Workplace: OnsiteFull timeFunction: Quality & Regulatory (Non-Software)Experience: 3-6 yearsEducation: bachelorsSkills: ["Analytical","Troubleshooting","Problem-solving","Attention to detail","Communication"]

Perform chemical and physical analysis of raw materials, semi-finished products, and stability samples in the Quality Control laboratory. Operate QC analytical equipment (e.g., HPLC, GC, UV-Vis, dissolution testing), ensure testing accuracy within timelines under GMP/GLP and pharmacopoeial standards, and maintain complete laboratory documentation with strong data integrity (ALCOA+). Enter results into SAP, support method validation/transfer, and assist QMS activities (CAPA, AMS, change controls) and audits.

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Julphar
Julphar
11 hours ago

Jr. Specialist- QC

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Source: Company careers pageValidated by: Fursa AI
Last checked: 11 hours agoStatus: Live
Reposted: similar role first listed 1 month ago

Job Summary

Perform chemical and physical analysis of raw materials, semi-finished products, and stability samples in the Quality Control laboratory. Operate QC analytical equipment (e.g., HPLC, GC, UV-Vis, dissolution testing), ensure testing accuracy within timelines under GMP/GLP and pharmacopoeial standards, and maintain complete laboratory documentation with strong data integrity (ALCOA+). Enter results into SAP, support method validation/transfer, and assist QMS activities (CAPA, AMS, change controls) and audits.
Location: United Arab Emirates
Workplace: Onsite
Employment Type: Full time
Job Function: Quality & Regulatory (Non-Software)
Seniority: Mid level

Key Responsibilities

  • •Perform chemical and physical analysis of raw materials, semi-finished products, and stability samples according to approved methods, specifications, and SOPs.
  • •Operate QC laboratory equipment (including HPLC, GC, UV-Vis spectrophotometers, dissolution apparatus) and ensure results are accurate and on time under GMP/GLP and regulatory requirements.
  • •Verify products meet quality specifications and pharmacopoeial standards (USP, EP, BP).
  • •Maintain complete records of analytical results and observations according to GDP, and enter results into SAP accurately and on time.
  • •Support QMS activities (CAPA, AMS, change controls) via AmpleLogic, participate in audits, and support closure of audit observations.

Key Requirements

  • •Bachelor's degree in Pharmacy, Chemistry, or a related Science discipline.
  • •3–6 years of relevant experience in pharmaceutical Quality Control.
  • •Hands-on experience with HPLC, GC, UV-Vis spectrophotometry, dissolution testing, and other analytical techniques.
  • •Strong knowledge of GMP, GLP, SOPs, and regulatory guidelines including USP, EP, and BP.
  • •Experience with analytical method validation, method transfer, and assay analysis with ALCOA+ data integrity and GDP documentation practices.
Experience:3-6 yearsPharmaceuticalQuality ControlGMPGLP
Education:Bachelor's in Pharmacy, Chemistry, or related Science
Skills:AnalyticalTroubleshootingProblem-solvingAttention to detailCommunication
Tech Stack:HPLCGCUV-Vis spectrophotometersDissolution apparatusUSPEPBPSAPAmpleLogicALCOA+GMPGLPSOPsCAPAQMSQMS activitiesAMSChange controls

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