LSC are current looking for a Validation Engineer for a 12 month contract position with our Orthopaedics Manufacturing client in Cork
The Validation Engineer will:
o Responsible for Design for Manufacture, ensuring conformance with current equipment, process, and systems validation regulations
o Responsible for determining the implications of validations upon; Product Quality, Patient Safety, and Data Integrity
o Responsible for completing Equipment Lifecycle documentation, URS, FS etc
o Participate in equipment, process, and software development and design review
o Responsible for determining and implementing control measures to reduce the occurrence and possible impact of failures
o Responsible for determining process inputs and factors for variation where process capability is required
o Responsible for calculating process capability
o Maintain, complete and accurate documentary evidence concerning Qualification and Validation exercises
The Validation Engineer requires:
o Degree level qualification in Engineering/Science or Equivalent
o Minimum 2-5 years post qualification experience as a Validation Engineer within a medical device, pharmaceutical, or similar regulated industry
o Experience in aspects of QA, validation and ISO 13485.
For more information on this Validation Engineer role, please call Ruth at LSC on 021 4777329, or apply directly via this ad.