Analytical Scientist

PE Global; Carlow; On-site; EUR 42,000 - 62,000; Full time

Job summary

PE Global is recruiting for an Analytical Scientist to join a leading pharmaceutical company in Carlow on an 11-month contract. The role focuses on end-to-end lifecycle management of analytical methods, including transfers, validations, investigations, and data documentation to support pipeline and commercial products.

You will contribute to cGMP compliance, data integrity, and cross-functional collaboration with QC, Manufacturing and Validation teams, applying chromatography, ELISA, and

Qualifications

• Bachelor's degree in a scientific discipline (analytical chemistry, chemistry, biochemistry, biotech, pharmaceutical sciences).
• Minimum 2-3 years' experience in pharma/biotech/vaccine industry in a GMP-regulated lab.
• Experience with analytical testing, data review, and technical documentation.

Responsibilities

• Support/Lead analytical method transfers, validations, and compendial method verifications.
• Perform laboratory-based analytical testing and technical studies using various techniques and instrumentation.
• Generate, review, interpret, and verify analytical data and technical documentation.
• Support lifecycle management and continuous improvement of analytical methods.
• Assist with troubleshooting of analytical methods and laboratory equipment.
• Participate in investigations, deviations, CAPAs, and change controls.
• Collaborate with Quality Control, Manufacturing, Validation, Technical Operations, and Global Analytical teams.
• Ensure compliance with cGMP, data integrity, safety, and regulatory requirements.

Skills

HPLC/UHPLC

ELISA

Cell Based Assay

Data analysis

GMP documentation and data integrity

Education

Bachelor's Degree in Analytical Chemistry, Chemistry, Biochemistry, Biotechnology, Pharmaceutical Sciences, or related field

Tools

Empower Software

Job description

PE Global is currently recruiting for an Analytical Scientist on behalf of a leading pharmaceutical company based in Carlow. This is an initial 11-month contract role.

Description:

The Site Analytical Sciences Associate Specialist/Specialist role is responsible for supporting Analytical Procedure Life Cycle through end-to-end method lifecycle management including introduction of new analytical methods, analytical transfers, SME assessment for all analytical method & equipment performance qualification, investigations, product testing and technical rationale. This work will support pipeline and commercial products by utilizing expertise in the analytical areas of separations and biochemistry.

Responsibilities:

• Support/Lead analytical method transfers, validations, and compendial method verifications.
• Perform laboratory-based analytical testing and technical studies using a variety of analytical techniques and instrumentation.
• Generate, review, interpret, and verify analytical data and technical documentation.
• Support lifecycle management and continuous improvement of analytical methods.
• Assist with troubleshooting of analytical methods and laboratory equipment.
• Participate in laboratory investigations, deviations, CAPAs, and change controls.
• Collaborate with Quality Control, Manufacturing, Validation, Technical Operations, and Global Analytical teams.
• Ensure compliance with cGMP, data integrity, safety, and regulatory requirements.

Education and Experience:

• Bachelor's Degree in Analytical Chemistry, Chemistry, Biochemistry, Biotechnology, Pharmaceutical Sciences, or a related scientific discipline.
• Minimum 2-3 years' experience within the pharmaceutical, biotechnology, or vaccine industry.
• Experience working in a GMP-regulated laboratory environment.
• Experience with analytical testing, data review, and technical documentation.
• Experience with method validation, method transfer, compendial testing, chromatography, electrophoresis, ELISA or analytical troubleshooting is advantageous.

Desired Technical Skills:

• HPLC/UHPLC (Agilent/ Waters)
• Empower Software Competency
• ELISA
• Cell Based Assay
• Compendial testing and Method Verifications
• Data analysis and technical report writing
• Laboratory investigations and root cause analysis
• GMP documentation and data integrity practices

***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland***