Scientist -Cell Culture

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:

Reporting through the site Process Sciences Lead,
Manufacturing Science and Technology and based at the  the Scientist’s responsibilities include, but
are not limited to the following:

Requirements

Responsibilities:

• Supporting and executing experimental design, data
  analysis and interpretation to resolve complex cell culture deviations.
  
• Supporting process improvement and troubleshooting with
  end -to -end product focus.
  
• Provide technical support investigations, new process
  introduction or change implementation in commercial manufacturing operations.
  
• Authoring and reviewing development operating procedures
  and technical reports.
  
• Supporting global regulatory submissions as needed.
  
• Applying LeanSixSigma tools in the Process Sciences group
  by:
  
• Securing continuity of an appropriate LSS/CEM level of
  knowledge.
  
• Facilitating problem solving & risk assessment (FMEA)
  projects/meeting.
  
• Making problems visible and strive for continuous
  improvement.
  
•  
  What skills you will need:
  
• A master’s degree (or higher) in Biological
  Sciences/Chemistry /Chemical Engineering/Biological Engineering.
  
• 0 -3 years’ experience in the Biopharmaceutical industry
  (preferably practical experience of cell culture processing).
  
• Experience in drug substance process development, process
  characterisation studies, mammalian cell technology, biochemistry, cell
  biology, fluid mechanics and process modelling.
  
• Experience in executing experimental programs in the
  laboratory.
  
• Working knowledge of statistical methods for DOE design
  and data analysis (e.g., JMP or Design Expert software)
  
• Experience with technology transfer, regulatory filing,
  and commercial drug substance manufacturing of biologics is a plus.
  
• Knowledge of and experience in applying Six Sigma and
  Lean methodologies
  
• Desirable evidence of Continuous Professional Development