Industry: Pharma/Biotech/Clinical Research Work Experience: 4-5 years City: Cork State/Province: Cork Country: Ireland Job DescriptionAbout PSC Biotech 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 points, 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 to 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 through Learning & Development in-house training mentorship through constant guidance to facilitate career progression. We believe in creating high-performing teams that can exceed our clients' expectations with regards to quality of all scalable and business unit deliverables, staying under budget and ensuring timelines for our deliverables are being met.
Job Description: An amazing opportunity has arisen for a Technical Support Analyst. They will provide validation (utilities PQ, equipment PQ, cleaning validation) and technical support to the Vaccines IPT team. The role will be reporting to the Vaccines IPT Associate Director.
RequirementsWhat you will do: Execute cycle development, cleaning validation, and PQ of equipment.Write and adhere to validation strategies, coordinate with outside vendors, write protocols independently, submit samples, analyze test results, and prepare technical reports.Execute business activities e.g. equipment periodic reviews, cleaning periodic review, CAPAs and deviations, change control, risk assessments.Provide support during commissioning phase by reviewing and approving documents. Ensure documentation complies with standards.Participate in cross-functional problem-solving teams for troubleshooting and investigations within Vaccines IPT.Technical report writing, statistical analysis of data.Adhere to the latest regulatory guidelines.Represent the IPT on cross-functional project teams.Provide technical input and support and present as an SME on relevant topics during regulatory inspections.Ensure compliance with the highest standards for Quality and Safety.Ensure compliance with site EHS policy, cGMP, and other business regulations and support Technical IPT input to risk assessments, audits, regulatory inspections, and incident investigations.Ensure the highest Quality, Compliance, and Safety standards by participating and complying with our Manufacturing Division Quality Management System (QMS) requirements, including ownership, as relevant.What skills you will need: 3-5 years' experience as a validation specialist in a pharmaceutical or a highly regulated environment and a B.Sc. Degree or other qualification in Chemical Engineering, Biochemistry, Microbiology, Chemistry, or a related field.Experience in at least three of the following areas: C&Q validation, Cleaning Validation, Equipment validation, Process operations or manufacturing, Process Engineering.A working knowledge of the GxP systems associated with this role would be advantageous. These include, but are not limited to: GLIMS and eVAL, electronic batch records.
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