Quality Operations API Intern at Bristol Myers Squibb in Dublin

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 This position involves working with the Quality Operations Global API team and providing support in documentation management. This role includes assisting in all stages of the document workflow, streamlining documentation management systems, supporting VPT associated operations, and interdepartmental communications. Responsibilities • Initiate, revise and evaluate change controls in respect of contract manufacturers • Support all activities associated with uploading and approval of protocols, reports, memos and other quality relevant documents in the Document Management System • Support preparation of Quality Agreements and purchase specs. • Support Annual Product Reviews submitted by the CMO’s and prepare for approval. • Support in providing information for quality council meeting • Follow corporate policies and directives. • Support audit observation closure. • Review and update CMO Bona Fides as required. • Support the update of annual risk assessments for CMOs as required. • Support the update of stability protocols as necessary. • Support quality related projects as required. • Manage the annual Batch Record Review-Requalification of CMOs. • Meet all targets related to BMS metrics. Required Competencies Minimum 2 years of relevant academic experience and knowledge in a science discipline (e.g., chemistry, pharmacy, micro-biology, or a related pharmaceutical degree). • Technical knowledge in chemical, biological and/or pharmaceutical operations which enables first-hand knowledge of manufacturing, quality control, quality assurance, regulatory affairs/sciences, and interface with research & development. • Knowledge of current Good Manufacturing Practices regulations. • Ability to build relationships and partnerships at external manufacturers. • Negotiation, communication and presentation skills across all levels both internal and external to BMS. • Analytical and problem-solving skills. 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