QC Sample Management Intern at Bristol Myers Squibb in Cruiserath

Job description

At Bristol Myers Squibb, our employees often ask, “Who are you working for?”—a question that fuels collaboration, accountability, and urgency in our work. Our purpose-driven culture inspires us to discover, develop, and deliver innovative medicines to prevail over serious diseases. We offer uniquely interesting and meaningful work, opportunities for growth, and a supportive environment that values inclusion, wellbeing, flexibility, and comprehensive benefits. This is work that transforms the lives of patients, and the careers of those who do it. Inspire and be inspired. We offer a variety of opportunities for undergraduate and post-graduate students to use your talent, skills, education and passion to help make an impact on patient’s lives – all while growing your career and earning academic credit. Our Internship Programme gives you a real opportunity to gain practical ‘hands-on’ experience, training and shadow the experts of your chosen field. It also provides you with insight into what it’s like to work with us. We will place you in a six, nine or twelve month Internship Programme depending on the requirements of your degree course. So, are you ready to embark on a new adventure? We can’t wait to see what you’re made of! Bristol-Myers Squibb is seeking to recruit a QC Sample Management Intern to join the QC Materials team at its Multi-Product Cell Culture Drug Substance Facility in Cruiserath, Dublin. Reporting to the QC Sample Management Manager, they will be responsible for supporting site activities related to the Sample Management Laboratory, in-process samples, retains and laboratory duties in accordance with cGMP regulations. The main responsibilities for this position include; · Liaise with manufacturing to ensure all Drug Substance samples are processed and delivered to the appropriate destination in an appropriate timeframe. · Liaise with Engineering Stores to ensure all Drug Product samples are processed and delivered to the appropriate destination in an appropriate timeframe. · Manage TempTales and shipping documents when receiving samples from external sites. · Logging of samples to LIMS/CIMS or logbooks, and label accordingly. · Storage of backups and reserve samples. · Perform monthly reconciliation and report deviations to Sample Management Manager, if any. · Support buffer preparation for the QC Separations lab · Generate and update SOPs and other relevant documents as required. · Maintain a high standard of GMP compliance including the completion and provision of training as required. · Keeps abreast of current corporate and industry requirements and compliance trends as they pertain to laboratory operations and aseptic manufacturing. · Support continuous improvement initiatives across the department and within the team · Performing any other activities as indicated by the Lab Manager. The successful candidate must demonstrate excellent written and verbal communication skills and the ability to work in a team based collaborative environment. The ideal candidate should hold a minimum of a third level qualification (Degree) in Chemistry/Biology or related discipline along with at least 1 year of experience in a pharmaceutical / healthcare labora. We hire for skills and capabilities, not just credentials – if this role excites you, but doesn’t perfectly match your resume, we encourage you to apply anyway. Compensation Overview: €14.94 per hour Pay for this internship/co‑op position is provided in accordance with local market practices and applicable laws. Pay may be offered as an hourly rate and/or monthly stipend, or other locally compliant structure. Pay is determined based on objective factors such as academic level, relevant experience, skills, and work location. Interns and co‑op participants may be eligible for limited benefits depending on program structure, work location, and local requirements. Eligibility and offerings are governed by applicable policies and employment regulations. This is a temporar