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
An amazing opportunity has arisen for a QC Analyst in Analytical Testing for one of our clients
our new state of the Art single use Multiproduct Biotech facility. In our start -up site the role will be
responsible for Quality Control testing and all associated laboratory activities related to
Biochemistry and Analytical Methods.
What you will do:
Bring energy, knowledge, innovation and influence to carry out the following:
· Perform a variety of routine Analytical
techniques and associated documentation; including but not limited to Capillary
Electrophoresis, UPLC, HPLC, GC, Wet Chemistry methods in compliance with GMP
requirements
· Support activities including general lab
readiness, audit readiness, laboratory equipment qualification and analytical
method technical transfer, verification and validation
· Drive the development of technical skills
through coaching and motivate a high performing culture across the team
· Foster a continuous improvement environment and
bring strong problem solving and troubleshooting capabilities
· Consistently deliver on specific area Key
Performance Indicators
· Operate to the highest standards of Safety,
Quality and Compliance
· Demonstrate a commitment to learning and
personal development that supports Quality,EHS, L&D and continuous
improvement
Requirements
What skills you will need:
In order to excel in this role, you will more than likely have:
· Degree qualification (Science/Quality/Technical)
· 2 -3 years’ experience in the biotechnology and/or pharmaceutical industry, particularly in
relation to Capillary Electrophoresis, UPLC, HPLC or GC testing
· Preferably Lean Six Sigma experience
· Ability to think logically and be proactive under pressure
· Ability to work as part of a team and on own initiative in a constructive manner
· Flexible and self -motivated