QC Chemistry Analyst

Company description: Use Your Power for Purpose Every day, our unwavering commitment to quality ensures the delivery of safe and effective products to patients. Our flexible, innovative, and customer-oriented culture is rooted in science and risk-based compliance. Whether you are engaged in development, maintenance, compliance, or research analysis, your contributions have a direct impact on patient care. Our dedication to quality and safety drives everything we do, fostering a dynamic environment where your role is crucial in advancing healthcare solutions. What You Will Achieve In this role, you will: You will be a member of Pfizers dedicated and highly effective quality control team. You will be responsible for activities involved in developing and maintaining quality programs, processes and procedures that ensure compliance with established standards and agency guidelines. Your contribution in quality risk management will help us in commitment tracking, interpreting policies, manage site complaints and work directly with operating entities to provide process analyses oversight. Thanks to you, we will be prepared for all upcoming audits and inspections. You will be relied on to ensure that the quality assurance programs and policies are maintained and modified regularly. You will make sure that there are uniform standards worldwide and best practice sharing, which will help in fostering the achievement of company's mission globally. You will be recognized as a subject matter expert with specialized knowledge and skills in procedures, techniques, tools, materials, and equipment. You will be entrusted with adapting standard methods and procedures by applying your knowledge, prior work experience and requirements. Your business awareness of cross-organizational impact on project delivery will elevate the quality of project deliverables. You will arrive at decisions on which methods and procedures are the best fit for different work situations. You will train others and reinforce behaviours that will help us achieve our goal of providing the best to patients. Job description: How You Will Achieve It: Perform analysis of quality control samples including, raw materials, In-process , intermediates, stability and finished product in line with Current Good Manufacturing Practices {part of GxP}. Write up and execute Analytical Method Transfer Exercises for products being transferred to the Grange Castle site, ensuring compliance with site, Pfizer Quality Standards (PQS), International Conference on Harmonization guidance and Filing requirements. Adhere to good laboratory practices and housekeeping standards. Assist in the generation and maintenance of Quality procedures and reports. Facilitate laboratory investigations and support associated product investigation. Analyse both wet chemistry and the use of analytical equipment including but not limited to, UV, HPLC, FTIR, KF, iCE, ICP, CE and compendial assays. Participate, and seek opportunities, in the areas of Right First Time, Continuous Improvement and unburdening activities to facilitate Lean/Agile implementation. Required profile: Here Is What You Need (Minimum Requirements) Third level Qualification in Science, Engineering or equivalent is preferred though not essential. Strong knowledge of analytical techniques both theoretical and practical Two years prior experience working in a GMP QC Laboratory environment. Excellent interpersonal and communication skills Detail oriented, quick at decision making, self-motivated with good trouble shooting and problem-solving abilities. What we offer: Work Location Assignment: Hybrid Additional Information In order to be considered for this position in Ireland you need to be legally eligible to work in Ireland. Please note there is no relocation support available for this position ? How to apply Make a difference today, all suitable candidates should apply with CV below. We are looking forward to hearing from you Skills: delivery manager Solution Delivery