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.