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.
A fantastic and exciting opportunity has arisen for a Manufacturing Biotech The Manufacturing BioTech Associate will work in amanufacturing self -directed shift team to deliver batch operationssuccessfully, identify and resolve issues in order to allow the site to deliverfor our patients in a culture that supportsQuality, EHS, Learning and Continuous improvement.What you will do:Bring your energy, knowledge, and innovation to:· The production ofbiologic drug substance on their designated shift team and will be responsiblefor the preparation, operation and monitoring of equipment, use ofbusiness systems and carrying out tasks including but not limitedto the cleaning, validation, in -process testing.· The progression of anautomated recipe using paperless technology in order to generate the drugsubstance through inoculation and cell culturing activities directing tofiltration and purification of the product.· Setting up the singleuse equipment between runs, carrying out the production process according toworld class GMP and EHS standards and driving to optimiseand improve the processing activities through use of standard work and leanprocessing techniques.· Focusing on deliveryto the patient through living the Dunboyne culture including a commitment tosafety, focusing on right first time in everything we do and concentrating onthe engagement and development of self and peers.
RequirementsWork ExperienceWhat skills you will need: A sciencequalification in a technical, engineering or science -based discipline orequivalent. to 3 years'experience in the biotechnology and/or pharmaceuticalindustry or equivalent. Experience ina highly regulated pharmaceutical manufacturing environment Goodunderstanding in the production of biologic drug substance and experiencean advantage. Ability to workas part of a shift team and on own initiative in a constructive manner. Abilityto think logically and be proactive under pressure. Flexible andself -motivated