QC Raw Materials 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! Position Summary Cruiserath Biologics are seeking to recruit an Intern for the QC Materials, QC Raw Materials team to support the QC teams at its Multi-Product Cell Culture Drug Substance Facility. Reporting to the QC Materials Manager, they will support the activities in the Projects team as defined below. Key Responsibilities Performing QC testing (TOC, pH Conductivity) of water samples. Performing analysis of Raw Materials using wet chemistry techniques. Completion in a timely and accurate manner of laboratory documentation as directed by the QC Material Management Supervisor. Compliance with Standard Operating Procedures and Registered Specifications. Assisting in authoring and reviewing documentation, including SOPs, as required. Batch paperwork review, and reconciliation of analysis performed in laboratory. Ensuring that any out of specification results are investigated according to site procedures. Assisting with out of specification investigations and deviations using the Infinity system. Sample management activities- ensuring chain of custody is maintained using CIMS and LIMS. Keeps abreast of current corporate and industry requirements and compliance trends as they pertain to laboratory operations and aseptic manufacturing. Performing any other activities as indicated by the Lab Supervisor. Qualifications & Experience Currently undertaking a third level qualification (Degree) in Science or related discipline. Experience with basic laboratory practices, such as use of pipettes, balances and pH meters. Demonstrate excellent written and verbal communication skills. Experience of working as part of a team and ability to work on own initiative. 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 temporary, time‑bound position intended for the duration of the internship or co‑op program and does not guarantee continued or permanent employment following program completion. How We Work Where you work matters – because collaboration, innovation and patient impact happen in many settings. Our roles are s