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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.
Qualifications:
Applications are invited from candidates who have a degree in Science (Chemistry Physics or related Life Science) and/or relevant experience.
Responsibilities:
Maintaining Analytical Laboratory instrumentation in validated state to support testing activities in accordance with site schedules and company policies procedures and guidelines.
The Instrumentation Specialist will review instrument calibrations to ensure uptime for all instruments supporting testing activities.
Provides a preventative maintenance service to ensure functionality and a calibration service to maintain the instruments according to their working specifications.
Ensures that all instruments are maintained in a validated state through a PM/PV schedule and ensuring that this schedule is adhered to by the Instrument group and contract vendors.
Be part of a dynamic team responsible for Data Integrity requirements for all computerised and noncomputerised systems across all the laboratories.
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