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 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.
What you’ll be working with:
Wonderware Intouch 9.5 SCADA – development, configuration, and support
Siemens S7 PLC programming and commissioning
APT software development and full project rollout
System integration across production and process control platforms
What you’ll be doing:
Managing and coordinating automation projects in a live 24/7 facility
Owning change control for automation and SCADA systems within a medical device regulated environment
Supporting Computer System Validation (CSV) and audit readiness activities
Troubleshooting and resolving automation faults to protect production continuity
Collaborating with Quality, Manufacturing, IT, and Validation teams
What we’re looking for:
Proficiency with Intouch 9.5, Siemens S7, and APT software – development through to deployment
Thorough knowledge of change control in a GMP/medical device regulated environment
Proven ability to manage projects in a high-volume, fast‑paced production setting
A self‑starter who takes ownership and works independently
Strong communication skills – comfortable engaging with technical and non‑technical stakeholders at all levels.
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