My client, a leading pharmaceutical company in Carlow, is expanding and seeking an Associate Quality Control Specialist to join their Incoming Quality team on a contract basis.
This role offers the opportunity to work in a fast-paced environment, supporting key quality processes and collaborating with global teams
Key Responsibilities:
Support the New Material Introduction process and supplier qualificationCoordinate and manage quality standards for raw materials and componentsCollaborate with external testing laboratories to ensure complianceSupport internal/external investigations and auditsContribute to lab capability improvements and efficiency projectsEnsure adherence to cGMP, cGLP, and company safety policiesWhat You'll Need:2-4 years' experience in a cGMP laboratory environmentStrong knowledge of New Material Introduction processesExcellent problem-solving and communication skillsBachelor's degree in Chemistry, Analytical Chemistry, or a related science disciplineExperience in method validation and transfer (a plus)This is an exciting opportunity to join a growing site, gain valuable industry experience, and contribute to high-quality pharmaceutical production.