Analytical / QC Technology Transfer Specialist

Fastnet; Munster; On-site; EUR 55,000 - 75,000; Full time

Job summary

Fastnet is seeking an experienced Analytical / QC Technology Transfer Specialist for a 12-month contract in Tralee, Co. Kerry.

The role centers on owning the analytical workstream for product transfers, with emphasis on method transfer and verification, ensuring QC collaboration and timely delivery. The successful candidate will have 4+ years in QC/Analytical within a GMP pharmaceutical setting, with hands-on transfer/verification experience and knowledge of ICH Q2; a related Chemistry/Pharma

Qualifications

• 4+ years' QC/Analytical experience in GMP pharmaceutical environment.
• Experience in analytical method transfer or verification.
• Knowledge of validation/transfer principles such as ICH Q2.

Responsibilities

• Own analytical method transfer/verification protocols and reports.
• Liaise with sending-site analytical teams for method packages, reference standards and data.
• Plan and track analytical method transfer activities with the product transfer schedule.
• Support analytical investigations and provide input into risk assessments.

Skills

QC/Analytical

Method Transfer

GMP Experience

ICH Q2

Education

Degree in Chemistry/Pharma

Job description

Analytical / QC Technology Transfer Specialist | 12-Month Contract | Tralee, Co. Kerry

Summary:

A 12-month contract opportunity in Tralee, Co. Kerry for an experienced QC/Analytical professional supporting a sterile pharmaceutical Technology Transfer programme. You'll take ownership of the analytical workstream for product transfers, with a particular focus on analytical method transfer and verification.

Key Responsibilities:

• Own analytical method transfer/verification protocols and reports, working closely with QC.
• Liaise with sending-site analytical teams to secure method packages, reference standards and comparator data.
• Plan and track analytical method transfer activities alongside the wider product transfer schedule.
• Support analytical investigations and provide analytical input into FMEA/risk assessments.

Requirements:

• Typically 4+ years' QC/Analytical experience within a GMP pharmaceutical environment.
• Experience in analytical method transfer or verification, with knowledge of analytical method validation/transfer principles such as ICH Q2.
• Degree in Chemistry, Biochemistry, Pharmaceutical Science or a related discipline; sterile fill-finish analytical experience is advantageous.