Career Opportunities

Position Description

QA Associate I
Job ID 11220
Location Athlone, IRE
Field Locations
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Applications are invited for a permanent role for a QA Associate I/II within the Quality Assurance Department reporting to the QA Manager. The key responsibilities of the role will cover both manufacturing and development areas and will include the following:

KEY RESPONSIBILITIES

  • Perform line clearance and GMP monitoring activities for pharmaceutical manufacturing and packaging processes ensuring compliance to cGMP standards.
  • Perform batch record review according to company procedures ensuring compliance to cGMP standards.
  • Adherence to, and ownership of, all cGMP, training and safety standards.
  • Making decisions specific to their area of work in a timely manner.

REQUIREMENTS

  • Third level qualification (Diploma Level 7 FETAC or higher) in Science related discipline with experience in a pharmaceutical environment, preferably in a Quality related role is desirable. 
  • Knowledge and experience of SAP, Sample Manager, Trackwise, Veeva, Ebr and Valgenesis or similar quality systems would be beneficial.
  • Conscientious and enthusiastic attitude.
  • Excellent attention to detail is an essential competency for this role.
  • Good written, verbal and interpersonal communication skills and the ability to effectively interact cross functionally.
  • Self-motivated with ability to handle changing priorities.
  • Availability to work shifts and overtime is essential.
  • Motivated, team orientated, flexible and quality focused.
  • Proven track record in your current role is essential.

 

 

 

 

Experience Level:
Associate
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