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:Reporting to the Digital Project Manager, specifically responsible for DeltaV Automation Systems delivery.This candidate will be required to work closely with the Digital teams responsible for the full Automation and IT scope and with vendors / partners with responsibility for delivery of systems. RequirementsRole Functions:As the DeltaV Lead Automation Engineer for the project, you will work with other Automation resources, Automation vendors and partners to deliver automation systems on time and within budget.Develop and/or review SDLC deliverables, compliant with standards, including but not limited to:Requirements SpecificationsRequirements Traceability MatrixFunctional SpecificationDesign SpecificationCode ReviewTest specification/test script Etc.Work closely with vendors of Automation equipment to ensure deliverables meet project requirements, including the interfacing of new Automation equipment with existing site systems, incl.
OEM automation systems, MES and PI HistorianWork closely with the DDQ and CSV functions and ensure their requirements are met in all deliverablesParticipate in Hardware and Software FATs and SATs to ensure requirements and standards are metFollow project schedules and document trackers to assist in the management and control of project deliverablesParticipate in Automation meetings and support relevant program meetingsLiaise with stakeholders on the overall project to ensure clear communication between all partiesEnsure Automation compliance with Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good Manufacturing Practices (cGMP) in the performance of dayto-day activities and all applicable job functions Knowledge, Skills, Education & Location RequirementsFluent in English, written and verbalMinimum of 5 years' experience in a similar role in the pharmaceutical industryStrong experience in the following systems: Emerson DeltaV incl.
core system implementation, base layer, batch layerKnowledge of and experience with the following systems would be advantageous; Siemens PLC/SCADA, OSISoft PI, Werum Pas-X, ABB DCS or other DCS systemsHybrid working option is a possibility.
The successful candidate may be required to attend periodic meetings or testing at vendor premises as requiredExcellent computer skills, proficient in the use of the following Microsoft tools: Excel, SharePoint, Word and PowerPoint.Strong interpersonal and communication skills (verbal and written)Relevant Computer Science or Engineering degree or equivalentPrevious experience of API or OSD manufacturing will be advantageousPrevious experience of high containment manufacturing will be advantageous#LI-AM1