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Quality Assurance Analyst

  • ... Posted on: Apr 22, 2026
  • ... Apsida Life Science
  • ... Flemish Region, Alberta
  • ... Salary: Not Available
  • ... Full-time

Quality Assurance Analyst   

Job Title :

Quality Assurance Analyst

Job Type :

Full-time

Job Location :

Flemish Region Alberta United States

Remote :

No

Jobcon Logo Job Description :

Apsida Life Science have partnered with a leading global pharmaceutical organization to present the following role:Company OverviewA global pharmaceutical organization specializing in the development and manufacture of active pharmaceutical ingredients (APIs), with a strong focus on quality, compliance, and supply chain excellence. The company operates within highly regulated environments, ensuring the highest standards across manufacturing, quality systems, and product release.Job Title – QA Analyst IILocation – Geel, BelgiumFunction – Supply Chain Quality (SCQ)Small Molecules experienceKey ResponsibilitiesReview and approve non-conformances and CAPAs in support of commercial QA operationsReview and approve GMP documentation including procedures, work instructions, protocols, and reportsProvide quality support to manufacturing and operational teams within the plantEnsure timely processing and compliance of quality records such as Change ControlsParticipate in QA check rounds and support ongoing compliance activitiesSupport continuous improvement and optimization projects within the QA functionCollaborate cross-functionally with Quality and Business stakeholders to ensure compliance and efficiencyRequirementsMaster’s degree in a scientific discipline (e.g., Chemistry, Pharmaceutical Sciences, Bioengineering)Proven experience within pharmaceutical or chemical quality assurance and/or supply chain environmentsStrong experience in non-conformance handling and CAPA managementSolid understanding of GMP regulations, ICH guidelines, and quality systemsKnowledge of end-to-end pharmaceutical processes including manufacturing, testing, release, and distributionAbility to work independently while effectively engaging with cross-functional teamsStrong analytical mindset with the ability to make risk-based decisions under pressureFluency in English and Dutch (both written and spoken)If you are interested in learning more, please reach out to Mufaro Life Science is a specialist recruitment business based in London (UK), Redhill (UK), Boston (USA) & Pretoria (South Africa) that is dedicated to delivering the best talent to the Life Science industry. We believe there is a gap in the market for a cost effective, high quality and trusted recruitment service that puts the candidate journey at the heart of the recruitment process.

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Jobcon Logo Position Details

Posted:

Apr 22, 2026

Reference Number:

25975_4401952557

Employment:

Full-time

Salary:

Not Available

City:

Flemish Region

Job Origin:

APPCAST_CPC

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Apsida Life Science have partnered with a leading global pharmaceutical organization to present the following role:Company OverviewA global pharmaceutical organization specializing in the development and manufacture of active pharmaceutical ingredients (APIs), with a strong focus on quality, compliance, and supply chain excellence. The company operates within highly regulated environments, ensuring the highest standards across manufacturing, quality systems, and product release.Job Title – QA Analyst IILocation – Geel, BelgiumFunction – Supply Chain Quality (SCQ)Small Molecules experienceKey ResponsibilitiesReview and approve non-conformances and CAPAs in support of commercial QA operationsReview and approve GMP documentation including procedures, work instructions, protocols, and reportsProvide quality support to manufacturing and operational teams within the plantEnsure timely processing and compliance of quality records such as Change ControlsParticipate in QA check rounds and support ongoing compliance activitiesSupport continuous improvement and optimization projects within the QA functionCollaborate cross-functionally with Quality and Business stakeholders to ensure compliance and efficiencyRequirementsMaster’s degree in a scientific discipline (e.g., Chemistry, Pharmaceutical Sciences, Bioengineering)Proven experience within pharmaceutical or chemical quality assurance and/or supply chain environmentsStrong experience in non-conformance handling and CAPA managementSolid understanding of GMP regulations, ICH guidelines, and quality systemsKnowledge of end-to-end pharmaceutical processes including manufacturing, testing, release, and distributionAbility to work independently while effectively engaging with cross-functional teamsStrong analytical mindset with the ability to make risk-based decisions under pressureFluency in English and Dutch (both written and spoken)If you are interested in learning more, please reach out to Mufaro Life Science is a specialist recruitment business based in London (UK), Redhill (UK), Boston (USA) & Pretoria (South Africa) that is dedicated to delivering the best talent to the Life Science industry. We believe there is a gap in the market for a cost effective, high quality and trusted recruitment service that puts the candidate journey at the heart of the recruitment process.

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