Specialist - QA (Sterile)

Julphar
United Arab Emirates
Workplace: OnsiteFull timeFunction: QA, Test & Release EngineeringExperience: 3-5 yearsEducation: bachelorsSkills: ["Accountability","Attention to detail","Communication","Collaboration","Task management"]

Ensure adherence to cGMP and maintain quality control across in-process production and packaging of biotech and sterile products. Investigate deviations, support CAPA, participate in media fills, and conduct line clearance checks while reviewing procedures with a quality mindset. Perform in-process inspections and equipment calibration verification, maintain accurate batch and QA records, input quality data into SAP, and contribute to internal and external regulatory audits and APQR reporting.

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Julphar
Julphar
3 hours ago

Specialist - QA (Sterile)

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Source: Company careers pageValidated by: Fursa AI
Last checked: 3 hours agoStatus: Live
Reposted: similar role first listed 4 weeks ago

Job Summary

Ensure adherence to cGMP and maintain quality control across in-process production and packaging of biotech and sterile products. Investigate deviations, support CAPA, participate in media fills, and conduct line clearance checks while reviewing procedures with a quality mindset. Perform in-process inspections and equipment calibration verification, maintain accurate batch and QA records, input quality data into SAP, and contribute to internal and external regulatory audits and APQR reporting.
Location: United Arab Emirates
Workplace: Onsite
Employment Type: Full time
Job Function: QA, Test & Release Engineering
Seniority: Mid level

Key Responsibilities

  • •Adhere to and enforce cGMP principles across in-process quality checks for production and packaging.
  • •Investigate deviations and support corrective and preventive actions (CAPA).
  • •Participate in media fills and ensure process compliance during production and packaging.
  • •Perform in-process quality checks, inspect incoming materials, and maintain accurate QA documentation including batch records.
  • •Input quality data into SAP, support APQR reporting, verify calibration of in-process check equipment, and participate in regulatory audits.

Key Requirements

  • •Bachelor’s or Master’s degree in Pharmacy.
  • •Knowledge of EU Annex-1 and cGMP requirements for sterile manufacturing.
  • •Minimum 3–5 years of experience in quality operations within sterile manufacturing.
  • •Proficiency with computer applications and QMS systems such as Agile, Trackwise, and Ampelogic.
  • •Strong command of English (written and spoken) and familiarity with risk assessment and quality compliance practices.
Experience:3-5 yearsSterile manufacturingBiotech
Education:Bachelor's in Pharmacy
Skills:AccountabilityAttention to detailCommunicationCollaborationTask management
Languages:English
Tech Stack:CGMPEU Annex-1SAPAgileTrackwiseAmpelogicQMSBatch recordsAPQR

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