Qc Bioanalytical Analyst

Details of the offer

Industry: Pharma/Biotech/Clinical ResearchWork Experience: 1-3 yearsCity: DublinState/Province: DublinCountry: IrelandJob DescriptionAbout PSC Biotech Ltd Who we are? 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 client's expectations regarding 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 QC Bioanalytical Analyst.
RequirementsRole Functions: Perform and carry out a variety of routine analytical techniques including but not limited to DNA PCR and Bioassay ELISA testing in compliance with GMP requirements.Follow up-to-date practices with reference to pharmacopoeias, specifications, regulations, and industry standards.Support the laboratory testing schedule to achieve an efficient QC system.Receive and manage samples that come into the lab for stability, in-process, and release testing.Reagent preparation, cleaning, and routine equipment maintenance.Maintain good housekeeping and hygiene within the laboratory.Calibrate and maintain all designated laboratory instruments.Participate in risk assessments, inspections, audits, incident investigations, etc., and implement and follow up on corrective/preventative measures.Ensure training is current for all job functions performed.Order, stock, and receive laboratory supplies.Maintain data integrity and ensure compliance with company SOPs, specifications, and cGMP regulations.Ensure that cGMP standards are always maintained.Promote and participate in the implementation and maintenance of the relevant safety programs.Experience, Knowledge & Skills: 1 - 5 years laboratory testing experience in the pharmaceutical industry.Relevant experience and skill set in their area of expertise that adds value to the business; ideally in a manufacturing, preferably in a GMP setting.Experience and critical skills in the area of expertise that add value to the business, ideally bioassay and DNA tests.Knowledge of regulatory/code requirements to Irish, European, and International Codes, Standards, and Practices.Knowledge of cGMP & Laboratory Quality Systems.Effective communication, presentation, and interpersonal skills, to interface effectively with all levels of colleagues and with external customers in a team-oriented manner.Qualifications & Education: Qualification in Science/Chemical Engineering/Biological Engineering
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