About PSC Biotech

Who we are?

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 points 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.

Job Title: QC Analyst in Analytical Testing

An amazing opportunity has arisen for a QC Analyst in Analytical Testing at our site. 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.

Requirements

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.

What skills you will need:

• 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 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