Specialist - QC

Julphar
United Arab Emirates
Full timeFunction: Quality & Regulatory (Non-Software)Experience: 3-6 yearsEducation: bachelorsSkills: ["Accountability","Communication","Interpersonal skills","Problem-solving","Attention to detail"]

Ensure GLP/GMP compliance in the QC laboratory, performing chemical and physical testing for raw, semi-finished, and stability samples. Operate QC equipment, record and enter analysis data in SAP, and verify final products meet specifications and regulations. Support audits, close observations, manage CAPAs/AMS/change controls in the Ample logic system, uphold data integrity and documentation practices, and execute daily lab activities aligned with EMS/EHS standards.

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Julphar
Julphar
2 days ago

Specialist - QC

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Source: Company careers pageValidated by: Fursa AI
Last checked: 14 hours agoStatus: Live
Reposted: similar role first listed 2 months ago

Job Summary

Ensure GLP/GMP compliance in the QC laboratory, performing chemical and physical testing for raw, semi-finished, and stability samples. Operate QC equipment, record and enter analysis data in SAP, and verify final products meet specifications and regulations. Support audits, close observations, manage CAPAs/AMS/change controls in the Ample logic system, uphold data integrity and documentation practices, and execute daily lab activities aligned with EMS/EHS standards.
Location: United Arab Emirates
Employment Type: Full time
Job Function: Quality & Regulatory (Non-Software)
Seniority: Mid level

Key Responsibilities

  • •Ensure and follow GLP/GMP, safety procedures, and maintain hygienic conditions in the QC lab.
  • •Carry out chemical and physical analysis for semi-finished/raw materials and stability studies, ensuring correct performance per procedures.
  • •Operate QC equipment for the relevant section and record all working data.
  • •Enter analysis data into SAP and ensure final products adhere to specifications and applicable regulations.
  • •Support audits, close observations on time, manage QC quality system actions (CAPAs, AMS, change controls), and uphold data integrity and documentation practices.

Key Requirements

  • •Bachelor’s degree in pharmacy or science.
  • •3–6 years of experience in QC/analytical testing in the pharmaceutical field.
  • •Proficiency with QC analytical instruments and techniques including HPLC, GC, and UV-Vis spectrophotometry.
  • •Strong knowledge of GMP, GLP, and regulatory guidelines (USP, EP, BP), including analytical method validation and transfer.
  • •Ability to maintain data integrity and good documentation practices (ALCOA+ compliance) and accurately document test results.
Experience:3-6 years
Education:Bachelor's in pharmacy/science
Skills:AccountabilityCommunicationInterpersonal skillsProblem-solvingAttention to detail
Tech Stack:SAPHPLCGCUV-Vis spectrophotometryAmple logicALCOA+

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