Project Engineer

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:

Provide project engineering services in support of the
commissioning and qualification of a drug substance and drug product
manufacturing facility. The job -holder works within the Global Engineering Team
to act as client representative to deliver integrated project engineering
services to meet the Project Objectives.

The Project Engineer will assist in the management of
cross functional teams to deliver a portfolio of assigned projects . 

Requirements

Responsibilities:

• Preparation of project related deliverables such as
  schedules, work plans, equipment cost tracking
  
• Coordination of project activities between stakeholders
  
• Manage installation / start -up / testing of key equipment
  systems through OQ completion.
  
• Interface with cross -functional team to ensure systems’
  post -OQ (PQ, PPQ) readiness.
  
• Monitor costs and progress of process suite team
  milestones with all team members and provide status reports to project Tiers
  and stakeholders.
  
• Support cross -functional project teams to ensure project
  and site stakeholder inputs and requirements are clear and reflected in design
  deliverables.
  
• Liaise with stakeholders, equipment vendors, business
  partners, and SMEs at other sites within the  Network as required to support Project.
  

Education/Experience Requirements:

• Minimum qualification B.Sc. or M.Sc./ M.Eng Degree in
  Engineering.
  
• Minimum of 6 years post academic engineering experience
  in relevant aseptic/sterile processing design and start -up environment.  
  
• Demonstrated ability to be a team player
  
• Excellent communication/presentation/organizational
  skills
  

Notes:

• This is a contract position. Estimated assignment
  duration is approx. 24 months, with initial 12 month contract.
  
• The position is based fulltime onsite at the Site The
  role may require small periods of travel to support vendor reviews. Flexibility
  is required in this regard.