Senior Manufacturing Bioprocess Associate

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 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 PropositionEmployees 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.Overview:An amazing opportunity has arisen for a Manufacturing Bioprocess Associate to provide operational support for manufacturing operations of the Late Stage and Launch Pipeline products at our new state of the art single use biotechnology facility .Responsibilities:The Senior Manufacturing Bioprocess Associate will support end-to end production operations for both Fed Batch and Continuous Manufacturing.Primary activities/responsibilities: Operate equipment according to electronic batch records, sampling plans and standard operating procedures.Work as part of a dedicated process team where flexibility and teamwork are a key requirement.Ability to solve problems with a desire to continuously learn, improve and develop.Support weekend or out of hours work on select time frames to support manufacturing activities.Conduct all work activities with a strict adherence to the safety and compliance culture on siteSupport the Authoring of electronic batch records, sampling plans, work instructions and standard operating procedures.Required Education, Experience and Skills:Level 7 qualification in a science or engineering discipline desired.A level 6 with a minimum of 3+ years’ experience in a GMP Manufacturing requirement shall be deemed equivalentCompetent in troubleshooting and show practical problem-solving capabilities.Ability to work independently and within a cross-functional team.Familiarity with contamination control and batch release requirementsFamiliarity with Emerson DeltaV, Pas X, and the use of Automation in a manufacturing Process.Proficiency in various SingleUse technologies in a manufacturing environmentPreferred Experience and Skills: Commissioning and Qualification experienceUnderstanding of Upstream and Downstream Unit Operations for mAb manufacturingUnderstanding of both continuous and batch fed manufacturing processesReports to: Drug Substance Process Operations Manager