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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 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.
An amazing opportunity has arisen for a Laboratory Systems Specialist
The Analytical Development and Commercialisation (ADC) department is responsible for all analytical support to the site. This involves testing of raw materials Excipients Components intermediates Drug Substance and Drug product.
The position reports to the Laboratory Systems Lead.
The position offers the opportunity to work with a team of professionals in a modern analytical laboratory using the most up to date technology and quality assurance procedures. The laboratory operates under Lean principles and employees the use of a wide variety of analytical techniques.
Responsibilities:
Compilation and completion of Analytical regulatory requests and data audits.
Management of the site reference standard and comparison system.
Maintenance of the site retain sample program and retain stores.
Support for the site stability program.
Oversight of the Vendor Manager inventory system for the ADC Laboratories.
Active member of the laboratory systems group and providing support and leadership to the group in team building safety compliance and improvement objectives.
Participate in assigned improvement projects.
What skills you will need:
In order to excel in this role you will more than likely have:
Applications are invited from candidates who have a degree in Science (Chemistry Physics or related Life Science) and/or relevant experience.
Have knowledge of GMP standards
Have knowledge Laboratory safety standards
Must have good communication skills both written and verbal.
Strong documentation skills are required.
Must be motivated focused and technically strong.
To maintain accurate records in compliance with GMP expectations
To understand and internalise procedures relevant to GMP operations
Communication written oral
Team and interpersonal skills
Full Time