QC NPI Senior Associate

QCS Staffing Ltd; Dublin; On-site; EUR 52,000 - 75,000; Full time

Job summary

QC NPI Senior Associate in Dublin, Ireland, for an initial 12-month contract within Life Sciences, supports NPI activities and QC project tasks across site operations. Responsibilities include representing QC in NPI meetings, planning tests, managing sample logistics, creating SOPs and documentation, and ensuring regulatory compliance.

The ideal candidate holds a Bachelor’s degree in science and has extensive biopharmaceutical QC or GMP laboratory experience, with experience in HPLC, rCE-SDS and

Qualifications

• Bachelor’s degree in a science discipline is required.
• Extensive biopharmaceutical QC or related GMP lab experience needed.
• Experience with cGMP manufacturing and testing of pharmaceutical products is essential.

Responsibilities

• QC Representative for NPI activities and routine Product meetings.
• Assist with QC projects or QC tasks within Site projects.
• Plan and perform non-core testing related to NPI activities.
• Manage all sample management activities related to NPI activities throughout the site.
• Create/own sample plans, SOPs and documentation related to NPI.

Skills

Data Integrity

GMP compliance

HPLC

rCE-SDS

Analytical technologies

Education

Bachelor’s degree in a science discipline

Tools

HPLC

rCE-SDS

Protein content

Job description

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

Our client, a globally recognised pioneer in Biotechnology, are recruiting for the contractual position of QC NPI Senior Associate. A leader in the industry, our client focuses on areas of high unmet medical need and leverages its expertise to stride for solutions. This is your chance to support them on their global mission to better the lives of those affected by disease and illness.

What you’ll deliver:

• QC Representative for NPI activities and routine Product meetings
• Assist with activities related to QC projects and/or QC tasks within Site projects
• Plan and perform non-core testing related to NPI activitiesManage all sample management activities related to NPI activities throughout the site
• Create/own sample plans, SOP’s and documentation related to NPI

Experience required:

• Bachelor’s degree in a science discipline.
• Extensive biopharmaceutical QC experience or related quality control or GMP laboratory experience in the pharmaceutical

Professional requirements:

• Demonstrated experience with current Good Manufacturing Practices, Data Integrity and sound analytical technologies (HPLC, rCE-SDS, Sub-Vis Particles, Protein Concentration/Protein Content)
• Experience with regulatory compliance in cGMP manufacturing and testing of pharmaceutical products.