QC Microbiology EM Intern

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 to 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!

During your placement as QC Microbiology Environmental Monitoring Intern you will get experience of working with our team and you will get exposure to various Quality Control activities such as:

• Data entry in laboratory electronic systems e.g. LIMS/MODA/LES
• Support QC Investigations and change controls
• Participate in the OpEx strategy and support process improvements
• Prepare and process QC documentation in quality documentation management system
• Performing Environmental Monitoring in Classified Areas (including lot related monitoring), Utility Sampling (Including WFI, Clean Steam and Compressed Gas), associated testing of samples and completion in a timely and accurate manner of laboratory documentation.
• Issuance, receipt, and testing of biological indicators.
• Reading and reporting of environmental monitoring, BIs, and aseptic qualification sample results.
• Ensuring that any alert/action limit excursions are investigated according to site procedures.
• Receipt and processing of drug substance and drug product samples.
• Adherence to and improvement upon lean lab and 6S practices.
• Ensuring a high standard of housekeeping and safety is maintained in the laboratory.
• Provide support to other departments to ensure qualification and production schedules are adhered to.
• Paperwork review, and reconciliation of analysis performed in laboratory. Ensuring that any out of specification results are investigated according to site procedures.
• Compliance with Standard Operating Procedures and Registered Specifications.
• Assisting in authoring and reviewing documentation, including SOPs, as required.

What Qualities Are We Looking For?

We are looking for highly motivated individuals who can collaborate in teams and have the willingness to learn.

• Biotechnology, Microbiology, Science / Biology, Chemistry or related discipline of study
• Passionate about the biopharma sector and innovation in healthcare
• Strong communication skills
• Ability to work as a member of a team
• Energetic, collaborative and dedicated .

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.