QC NPI Specialist

QCS Staffing; Dublin; On-site; EUR 60,000 - 85,000; Full time

Job summary

QCS Staffing in Dublin is seeking a QC NPI Specialist for an initial 12-month contract within the Life Sciences sector. The role focuses on supporting a pharmaceutical organisation through cGMP-compliant lab activities and NPI initiatives.

You will perform lab functions, follow transfer and validation protocols, troubleshoot new methods, and ensure training remains current while providing QC SME guidance to the NPI team.

Qualifications

• Deep knowledge of current regulatory requirements for Chemistry or Biochemistry methods in support of cGMP operations.
• Strong technical knowledge in Biochemistry or Chemistry.
• Experience in investigation methodology and method troubleshooting.
• Ability to follow written procedures with close attention to detail.
• Good report writing and technical writing skills.

Responsibilities

• Perform all lab functions in compliance with cGMP.
• Follow written protocols for Transfer and Validation activities.
• Troubleshoot new methods as required.
• Ensure training is current for all job functions performed.
• Provide QC SME and day to day technical guidance for NPI activities.
• Support the NPI management team as required.

Skills

cGMP knowledge

Analytical skills

Documentation accuracy

Technical writing

Education

Chemistry or Biochemistry degree

Job description

QC NPI Specialist – Ireland, Dublin – Initial 12-Month Contract – Life Sciences

Are you looking for the chance to support a life changing pharmaceutical organisation in their mission to continuously drive innovation? We are recruiting for a QC NPI Specialist to support a project in Dublin on an initial 12-month contract.

What You’ll Deliver

• Perform all lab functions in compliance with cGMP
• Follow written protocols for Transfer and Validation activities
• Troubleshoot new methods as required
• Ensure training is current for all job functions performed
• Provide QC SME and day to day technical guidance for NPI activities
• Support the NPI management team as required

Experience required:

• In depth knowledge of current regulatory requirements for Chemistry or Biochemistry methods in support of cGMP operations supporting clinical and commercial manufacturing
• Good technical knowledge in the area of Biochemistry or Chemistry.
• Good experience in investigation methodology and method troubleshooting
• Ability to follow written procedures with close attention to detail
• Good report writing and technical writing skills.