Specialist Engineering & Compliance Services

As one of Synertec's longest industry presence, Synertec is recognised as an industry leader within the Life Sciences for engineering as well as compliance and validation services.

Synertec’s Quality & Validation team comes with extensive consulting experience within cGMP-regulated departments of pharmaceutical companies. Clients benefit from the efficiencies of Synertec as a partner, who can deliver outcomes in all cGMP critical systems in-house, under the one management, quality and validation system.    

Synertec's engineering teams have been involved in major projects around the world delivering state of the art pharmaceutical manufacutring facilities.

Specialist expertise is offered in

  • Process & Mechanical Engineering
  • Construction Management
  • Production Modelling
  • Compliance & Validation

Core Capabilities


  • Pharmaceutical Manufacturing Facilities
  • Clean Room Environments
  • Research Laboratories
  • Storage Facilities
  • BioSecurity / AQIS Facilities

  • Computer System Validation
  • Utilities design, commissioning and validation
  • FDA, EMEA, ICH, and PIC/S Good Manufacturing Practices (GMP) with their regional interpretation by TGA, Medsafe, HAS and NPCP
View pharmaceutical case studies