Drug Product QP Operations Cruiserath Intern at Bristol Myers Squibb

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! Key responsibilities will include: - Support the Qualified Person with the Batch Certification function - Prepare and review batch documentation packages for QP release as per SOP requirements - Liaise with BMS Supply Chain and Quality colleagues to ensure that disposition lead times are consistently met - Update SOPs, controlled documents i.e. FORMS and OJTs - Assist in new product introduction activities as required - Provide training to new team members - Support the site inspection readiness program for corporate and regulatory inspections - Identify and make recommendations for improvements to ensure continuous improvement - Participate in site activities associated with the QMS (e.g. Change Control, Self-Inspections, Quality Agreement updates, Customer Complaints, Product Quality Record Reviews) as required - Ensure that all work carried out follows the required standards conforming to SOPs, regulatory regulations and guidelines, and Quality Agreements - Perform additional team tasks as agreed to support effective running of the function - Provide support to QA Senior Specialists throughout their activities. Qualifications and Experience required: - Strong working knowledge of Microsoft Excel and PowerPoint - Ability to work on his/her own initiative in addition to working as part of a team - Good organizational skills and attention to detail - Ability to handle multiple assignments and changing priorities - Ability to learn and utilize computerised systems for daily performance of tasks - Ability to prioritize, manage multiple tasks, and meet deadlines - Employees are expected to display the BMS Biopharma Behavior’s, which enable them to be successful and perform at their highest level. 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 im