Analytical Science Associate/Specialist — Lab & Validation

Life Science Recruitment; Carlow; On-site; EUR 42,000 - 54,000; Full time

Job summary

Life Science Recruitment is recruiting for an award-winning pharmaceutical organization in Carlow for Analytical Science Associate & Specialist roles. This onsite role is based in Carlow and initially for 11 months.

You will lead method transfers, validations, and testing, generate and review data, ensure cGMP compliance, and collaborate with QA, Manufacturing and Global Analytical teams to drive method improvements.

Qualifications

• Bachelor’s degree in Analytical Chemistry, Chemistry, Biochemistry, Biotechnology, Pharmaceutical Sciences, or related field.
• 2–3 years for Associate level and 3–5 years for Specialist level in pharmaceutical/biotech/vaccine industry.
• GMP-regulated laboratory experience; experience with analytical testing, data review, and documentation.

Responsibilities

• Support/Lead analytical method transfers, validations, and compendial verifications.
• Perform laboratory-based analytical testing and technical studies using a variety of techniques.
• 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.
• Support PQ activities and involve 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.
• Support digital method development.

Skills

Analytical Chemistry

GMP experience

Data interpretation

Method transfer

Education

Bachelor's Degree in Analytical Chemistry / related field

Job description

Life Science Recruitment is recruiting for an award-winning pharmaceutical organization in Carlow for Analytical Science Associate & Specialist roles. This onsite role is based in Carlow and initially for 11 months.

You will lead method transfers, validations, and testing, generate and review data, ensure cGMP compliance, and collaborate with QA, Manufacturing and Global Analytical teams to drive method improvements.