About PSC BiotechWho 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 PropositionEmployees 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 in 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 improvementRequirementsWhat skills you will need:In order to excel in this role, you will more than likely
have:Degree qualification (Science/Quality/Technical)1-3 years’ experience in the biotechnology
and/or pharmaceutical industry, particularly in relation to Capillary
Electrophoresis, UPLC, HPLC or GC testingPreferably Lean Six Sigma experienceAbility 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