THE ROLE
Designing, executing and reporting on periodic qualification program.
Designing, executing and reporting on periodic requalification studies for equipment, systems and processes.
Ensuring periodic qualification studies are managed in conjunction with all required Sanofi standards and legal requirements (Health & Safety, cGMP, construction, environmental etc.)
Providing technical interpretation and guidance of current US FDA and EU validation requirements for aseptic processing, lyophilisation, sterilisation and depyrogenation.
Ensuring that the validation status of equipment and systems are in compliance with cGMP at all times.
Participation in external regulatory inspections.
Support Site Change Control process.
REQUIREMENTS
Degree in Science (Chemistry, Micro. or Pharmacy preferred) or Engineering Chemical/Mech/Elec).
Experience: 3-5 years’ experience working in a Healthcare manufacturing environment – ideally part of which would be in the pharmaceutical sector.
Capable of troubleshooting validation issues associated with projects, process development etc.
Competent technical knowledge of pharmaceutical plants.
Previous validation/product development experience would be highly advantageous for the role.
Knowledge of requirements for of GAMP, ISPE Baseline guides.
Knowledge of steam and dry heat validation publications such as AAMI/ANSI, PDA and ISO guidelines.
please call Louise Mulligan today for further information on 0949003979 or email: lmulligan@careerwise.ie
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