Social network you want to login/join with: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 LevelPSC Biotech disrupts the conventional consultancy model by aligning our Employee Value Proposition as a key differentiator, offering the opportunity to work with talented professionals in the Pharma/Biotech industry. We provide permanent employment contracts with exposure to top pharmaceutical client sites in diverse cultural settings.Employee Value PropositionEmployees are the "heartbeat" of PSC Biotech. We support career development through in-house training, mentorship, and guidance to facilitate growth. We aim to create high-performing teams that exceed client expectations in quality, stay within budget, and meet deadlines.Overview:We have an exciting opportunity for an Analytical Scientist R&D at our Dunboyne facility. This role involves working with the Enabling Technology and Engineering group to leverage Process Automation and with the Analytical group to adopt Process Analytical Technology (PAT). The Microbiology Lab Operations team will collaborate with Operations to understand facility requirements and adapt resources accordingly.This is a shift-based role (4 days on / 4 days off, 7-day rolling shifts from 7 am to 7 pm).RequirementsResponsibilities:Manage laboratory operations, including equipment qualification (PQ), documentation, SOP review, and process establishment.Review and lead trending and reporting of laboratory data to support batch release and generate reports.Maintain and order laboratory stock and consumables.Participate in functional, departmental, and cross-functional meetings.Support internal and external audits and inspections to ensure readiness.Promote safety and a positive working culture respecting diverse populations.Perform GMP activities, troubleshooting, and execute in-process and drug substance analysis studies.Support the introduction of innovative solutions and lean lab methodologies.Organize testing schedules and meet deadlines.Foster team effectiveness and promote success through actions and training.Support changing business needs, including occasional out-of-hours testing.Skills & Qualifications:Degree in Biological Sciences, Engineering, or related field; MSc preferred.3+ years of relevant industry experience.Ability to work well in a team and independently.Knowledge of biologics manufacturing and microbiological testing techniques.Logical thinking and proactive under pressure.
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