Basic Role Summary:This is an opportunity to be part of a dynamic team within the Product Launch function. We are looking for individuals who will support and drive Chanelle Pharma's vision to be the most valued global provider of high‑quality, competitively priced pharmaceutical products and to provide excellent services and support to our customers.In this role, you will report into the Product Launch Team Leader.Location: Onsite at our facility in Loughrea.As our Product Launch Coordinator, your key responsibilities will be as follows:Project manage the introduction of new products into our manufacturing facility and 3rd‑party manufacturing partners for supply to customers worldwide.Coordinate and schedule product transfers from external sites to Chanelle's manufacturing plant.Liaise with customers before, during, and after product transfer/product introduction to ensure all requirements are captured and executed to the customer's satisfaction.Interact frequently with Artwork, Regulatory, Manufacturing, Operations, Engineering, QA, and Quality Control personnel as required.Plan, direct, and monitor launch projects against schedule within agreed costs and in accordance with company and customer deadlines.Identify with department managers the necessary requirements to successfully introduce new products and customers to Chanelle.Assess packaging requirements and determine the appropriate packaging strategy in conjunction with customers and internal departments.Travel to meet external customers on an ad‑hoc basis as required to strengthen business relationships.Suggest and implement improvements to existing Chanelle processes.Support the Product Launch Manager as required.Ensure all work is carried out in compliance with required standards, including GMP, Health & Safety, Environmental, and regulatory requirements.Use the Quality Management System (Q‑Pulse) daily to set up, monitor, and close out LCFs, Deviations, and CCFs.Qualifications and Experience:Third‑level qualification.Proficiency in Microsoft Word, Excel, and Outlook essential.Systems experience desirable.Experience in project coordination within a pharmaceutical cGLP environment, with knowledge of EU GMP and US FDA guidelines (preferable but not essential).Skills and Competencies:Excellent written and communication skills.Excellent attention to detail.Strong interpersonal, communication, and collaboration skills.Flexible and adaptable to new responsibilities and challenges.Excellent organisational skills with the ability to prioritise workload.Applicants from diverse backgrounds, including those returning after a career break or with transferable skills from non-traditional career paths, are encouraged to apply. We value varied experiences and are committed to fostering an inclusive environment that supports individuals with disabilities.