LSC have a great contract opportunity for a QA Specialist to join a leading biotech company based in Cork!
If you have previous QA experience within the Pharmaceutical/Biotech industry then this could be the perfect contract for you!
This QA Specialist position is responsible for carrying out tasks and projects related to management of Quality Assurance activities as required by Good Manufacturing Practice (GMP). In this position you will provide support and direction to all departments in respect of specific quality system elements to ensure business, quality and compliance goals are met and partner with other departments to ensure that compliance systems are implemented in an efficient manner.
Key Responsibilities: In this QA Specialist role you will be responsible for:
o Batch Record Review & material release to ensure compliance with GMP requirements.
o Carries out tasks related to the administration of event management systems including Review & Approval of Event, Deviations, and Customer complaints.
o Carries out tasks related to the management of batch records design and approval.
o Carries out administration of the SAP Quality Management Module.
Are your skills a match for this QA Specialist position?
o Bachelor’s Degree in a scientific/technical discipline
o Experience in a quality role within the biological and/or pharmaceutical industry.
If you are interested in hearing more on this QA Specialist role, please contact Regina at [email protected], or apply directly through this advert.