Senior QC Analyst in Analytical Testing

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 cloudbased 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 likeminded 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 diversecultural work setting.

Employee Value Proposition
Employees are the heartbeat of PSC Biotech we provide unparalleled empowering career development though Learning & Development inhouse 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 Description:

An amazing opportunity has arisen for a Senior QC Analyst in Analytical Testing at our client facility. In our startup site the role will be responsible for Quality Control testing and all associated laboratory activities related to Biochemistry and/or 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.
  
• Review and approve Analytical Testing data.
  
• 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).
  
• 35 years experience in the biotechnology and/or pharmaceutical industry particularly in relation to Capillary Electrophoresis UPLC HPLC CE and or raw materials testing.
  
• 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 selfmotivated.
  
• Problem solving abilities and change agile.
  

#LIXA1

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. Review and approve Analytical Testing data. 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). 3-5 years experience in the biotechnology and/or pharmaceutical industry, particularly in relation to Capillary Electrophoresis, UPLC, HPLC, CE and or raw materials testing. 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. Problem solving abilities and change agile.