Technical Administrator

Job Description

About PSC Biotech

 

Who are we?

PSC Biotech is a leading Biotech Consultancy firm founded in 1996, headquartered in Pomona, California, USA, with Global operations in Ireland, India, Singapore, Australia and the US, serving 350 clients in more than 23 countries worldwide. We provide cloud-based software solutions for Quality Management and Regulatory Inspections, pharmaceuticals contract manufacturing professionals, and metrology services to our clients.

 

‘Take your Career to a new Level’

PSC Biotech disrupts the conventional consultancy model by aligning our EVP as one of the unique selling point which includes the opportunity to work with the most talented cohort of like-minded professionals operating in the Pharma/ Biotech Industry. We offer a permanent contract of employment giving exposure of working in Top Pharmaceutical client sites in a diverse-cultural work setting.

 

Employee Value Proposition

Employees are the “heartbeat” of PSC Biotech, we provide unparalleled empowering career development though Learning & Development in-house training mentorship through constant guidance to facilitate career progression. We believe in creating high performing teams that can exceed our client’s expectations with regards to quality of all scalable and business unit deliverables, staying under budget and ensuring timelines for our deliverables are being met.

Overview:
The Technical Administrator will work within the Maintenance Systems team to keep the Engineering Documentation and CMMS (Computerised Maintenance Management System) updated.

Requirements

Responsibilities:

• Manage documentation related to Maintenance Systems for the site handed over from Projects (e.g. P&IDs, OEM manuals, etc)
  
• Register new equipment and instrumentation on the CMMS (SAP & Procal) following change control procedures.
  
• Work with stakeholders on the approval and execution of the above.
  

 

Skills Required:

• Good organisational and data management skills.
  
• Experience / proficiency in document management systems and office applications. 
  
• Experience working in a GMP environment and quality management systems.
  
• Familiar with Maintenance Systems structure and applications.
  
• Analytical mindset, data driven with attention to detail on systems.
  

#LI-XA1

 

Requirements
Manage documentation related to Maintenance Systems for the site handed over from Projects (e.g. P&IDs, OEM manuals, etc) Register new equipment and instrumentation on the CMMS (SAP & Procal) following change control procedures. Work with stakeholders on the approval and execution of the above.

---