Biopharma QC Scientist – GMP & HPLC Expert

Eurofins; Dungarvan; On-site; EUR 36,000 - 56,000; Full time

Benefits offered by this job

Private medical insurance

Income protection

Life assurance

Free parking

Additional leave days

Work-life balance

Sports & social events

Career progression

Job summary

Eurofins Biopharma Product Testing in Dungarvan, Co. Waterford is seeking an Associate Scientist to join the biopharma team. The role focuses on quality control testing of pharmaceutical and biopharmaceutical products to ensure safety and compliance with GMP.

You will perform routine and non-routine analyses, document test results, support continuous improvement, and train colleagues as needed. Weekend rota, overtime and on-call duties may be required.

Qualifications

• 1 to 3 years GMP experience.
• Strong attention to detail.
• Excellent documentation and record-keeping skills.
• Ability to work independently and in a team.
• Good communication skills and client focus.

Responsibilities

• Perform routine and non-routine analysis with accuracy and efficiency.
• Complete test records on time, ensuring SOPs and regulatory standards.
• Identify opportunities for quality and service improvement; contribute to CI projects.
• Adhere to GMP guidelines and internal quality standards; ensure all activities are documented and traceable.
• Participate in Root Cause Analysis and prepare Exception reports.
• Gain proficiency in assigned tests/areas of testing; maintain training records.
• Provide training to colleagues in techniques/tests where competency is proven.
• Provide cover for colleagues as required.
• Participate in weekend rota, overtime, and On-Call/Call-out schedules.
• Ensure customer requirements.

Skills

GMP experience

Attention to detail

Documentation skills

Teamwork

Communication skills

Proactive

Tools

HPLC

Biologics testing

Job description

Eurofins Biopharma Product Testing in Dungarvan, Co. Waterford is seeking an Associate Scientist to join the biopharma team. The role focuses on quality control testing of pharmaceutical and biopharmaceutical products to ensure safety and compliance with GMP.

You will perform routine and non-routine analyses, document test results, support continuous improvement, and train colleagues as needed. Weekend rota, overtime and on-call duties may be required.