Molecular Cell Biology QC Scientist (GMP)

Eurofins Biopharma Product Testing Ireland; Dungarvan; On-site; EUR 40,000 - 60,000; Full time

Benefits offered by this job

Private Medical Insurance

Income protection

Life assurance

Free parking onsite

Additional annual leave

Work-life balance

Sports and Social events

Job summary

Eurofins Biopharma Product Testing Ireland in Dungarvan is seeking an Associate Scientist to join the Molecular Cell Biology Team. The role focuses on quality control testing of pharmaceutical and biopharmaceutical products to ensure compliance with predefined quality and safety standards.

You will perform routine and non-routine analyses, maintain accurate test records, and contribute to continuous improvement while adhering to GMP guidelines.

Qualifications

• Degree in molecular cell biology or related discipline.
• At least 2 years experience with Cell Based Potency assays in GMP.
• Strong documentation skills and GMP understanding.
• Ability to work independently and in a team.

Responsibilities

• Carry out quality control testing of pharmaceutical and biopharmaceutical products to ensure compliance with predefined quality and safety standards.
• Perform routine and non-routine analyses with accuracy and efficiency.
• Complete test records on time, ensuring compliance with SOPs and regulatory standards.
• Identify opportunities for quality and service improvement; contribute to continuous improvement projects.
• Adhere to GMP guidelines and internal quality standards; ensure all activities are documented and traceable.

Skills

Detail-oriented

Excellent communication

GMP awareness

Team player

Independent worker

Education

Degree in molecular cell biology or related

Job description

Eurofins Biopharma Product Testing Ireland in Dungarvan is seeking an Associate Scientist to join the Molecular Cell Biology Team. The role focuses on quality control testing of pharmaceutical and biopharmaceutical products to ensure compliance with predefined quality and safety standards.

You will perform routine and non-routine analyses, maintain accurate test records, and contribute to continuous improvement while adhering to GMP guidelines.