Jr. Specialist - QC

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

Ensure cGMP/GLP/GMP compliance within the Quality Control division by performing chemical and physical analyses for finished products, raw materials, and stability samples. Operate QC equipment, create and process HPLC/GC methods and analytical data, and maintain accurate records in SAP. Support investigations, CAPA/deviation/OOS actions via Amplelogic, and contribute to audits by reviewing/approving validation and stability documentation while training QC personnel and qualifying analysts.

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Julphar
Julphar
15 hours ago

Jr. Specialist - QC

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Last checked: 15 hours agoStatus: Live

Job Summary

Ensure cGMP/GLP/GMP compliance within the Quality Control division by performing chemical and physical analyses for finished products, raw materials, and stability samples. Operate QC equipment, create and process HPLC/GC methods and analytical data, and maintain accurate records in SAP. Support investigations, CAPA/deviation/OOS actions via Amplelogic, and contribute to audits by reviewing/approving validation and stability documentation while training QC personnel and qualifying analysts.
Location: United Arab Emirates
Workplace: Onsite
Employment Type: Full time
Job Function: Quality & Regulatory (Non-Software)
Seniority: Mid level

Key Responsibilities

  • •Adhere to and maintain cGMP principles, including following GLP/GMP/safety procedures and maintaining hygienic lab conditions.
  • •Perform chemical and physical analysis for finished products, raw materials, and stability samples, and support process validation.
  • •Operate QC equipment (by QC section) and ensure correct execution of analyses as per applicable procedures.
  • •Enter, record, review, and approve working data and analytical results in SAP, including locking results and managing audit trail checks for instruments.
  • •Create and process HPLC/GC analytical methods and outcomes, investigate lab incidents/OOS/OOT/deviations, and support audits by closing observations on time.

Key Requirements

  • •Bachelor’s degree in pharmacy or science.
  • •Minimum 3–6 years of experience in Quality Control within the same field.
  • •Adhere to cGMP principles and ensure GLP/GMP/safety compliance in lab operations.
  • •Conduct chemical and physical analysis for raw materials, finished products, and stability samples using QC equipment.
  • •Proficient in computer applications and capable of maintaining accurate data entry/recording (SAP).
Experience:3-6 yearsPharmaceuticalsQuality controlGxP
Education:Bachelor's in pharmacy/science
Skills:AccountabilityAttention to detailsCommunicationInterpersonal skillsProblem-solving
Tech Stack:SAPHPLCGCAmplelogicGLPGMPCGMPHygieneMethod validationMethod transferProcess validationStability

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