The Process Improvement and Validation Engineer provides support to the Operations group, primarily in relation to process equipment/systems and remanufacturing validation matters. Support is provided as requested by staff within the group, and may generally be in the form of the following types of activity: Routine and emergency maintenance/calibration/troubleshooting Equipment modification/improvement projects, New equipment Preparing and reviewing validation documentation and other GMP documentation Completing routine, general activities within the Operations group as required Duties Contributing to incident investigations, risk assessments, and similar activities that may require input from multiple perspectives, including an engineering perspective; Reviewing maintenance calibration and other records of routing Devising and implementing modifications/improvements to equipment/systems, Selecting, procuring and installing new equipment, and completing pertinent Change Control activities, Preparation and/or review of documentation, e.g. procedures, records and reports About You! Must come from a Pharmaceutical Industry and have recent experience GMP Certified is essential Hold a Mechanical or Maintenance Engineer qualification MUST be a Permanent Resident or Australian Citizen Able to be hands on and be on the tools On Offer Permanent position, Frenchs Forest location Work with a reputable long standing pharmaceutical brand $100K Super, onsite parking Great staff incentives 6am - 2pm Mon - Fri Apply NOW! For a call back to discuss further if you meet the above requirements.
