QC NPI Analyst: Pharma Analytical Launch Specialist

PSC Biotech Corporation

Galway

Hybrid

EUR 42,000 - 62,000

Full time

14 days+
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Job summary

PSC Biotech Corporation in Ireland is seeking a QC Analyst to join the Quality Control New Product Introduction function. You will support analytical testing of raw materials, APIs and excipients, ensuring GMP compliance and timely delivery of methods and data.

The role requires a bachelor’s degree in a chemistry-based discipline, 3+ years in a pharma cGMP environment, and strong documentation and collaboration skills to work with R&D, QA and regulatory teams.

Qualifications

  • Bachelor’s degree in chemistry-based discipline.
  • 3+ years of experience in an R&D/QC analytical role in pharma.
  • Experience in a cGMP/cGLP environment and regulatory familiarity.
  • Experience with analytical method transfers and validations.

Responsibilities

  • Perform analytical testing of Raw Materials, API and Excipients using approved procedures.
  • Carry out testing in GMP-compliant laboratory with proper documentation and safety practices.
  • Plan, prioritise and execute analytical activities to meet R&D and NPI timelines.
  • Prepare ECPs and support Vendor Approval processes.
  • Maintain GLP standards and ensure accurate data recording and filing.
  • Communicate results to R&D, QA, Regulatory and Purchasing teams.

Skills

Analytical chemistry
Laboratory testing
Documentation
Team collaboration

Education

Bachelor's degree in chemistry-based discipline

Tools

HPLC
GC
Analytical method transfer
Method validation

Job description

PSC Biotech Corporation in Ireland is seeking a QC Analyst to join the Quality Control New Product Introduction function. You will support analytical testing of raw materials, APIs and excipients, ensuring GMP compliance and timely delivery of methods and data.

The role requires a bachelor’s degree in a chemistry-based discipline, 3+ years in a pharma cGMP environment, and strong documentation and collaboration skills to work with R&D, QA and regulatory teams.

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