Bristol Myers Squibb - Graduate CMC Technical Writing Programme

At Bristol Myers Squibb, we work every day to transform patients’ lives through science. In 2019, Bristol Myers Squibb acquired Celgene; we combine the reach and resources of an established pharmaceutical company and the agility of a biotech to create a global leading bio-pharma company powered by talented individuals who drive scientific innovation.

Our Graduate Programme:

If you have an undergraduate or post-graduate degree gained between 2022 to 2024, consider our graduate programmes. Get ready to learn, grow and share ideas that can bring hope to patients battling diseases. Our graduate offering is a major step towards a career you’ll find fulfilling, both professionally and personally. Our one-year and two-year programmes are designed to ensure you gain valuable industry and functional experience, work on challenging assignments, and network with our remarkable Bristol Myers Squibb employees, whilst learning about our company.

You possess a unique and fresh perspective with a passion for excellence. See just how far your talent will take you. Put your qualification to work at Bristol Myers Squibb where your skills and education can help patients prevail over serious diseases

What will I be doing on this role?

You will work in the Chemistry Manufacturing and Control (CMC) Documentation and Specifications Group within the Analytical Strategy and Operations Team at Moreton. You will support and/or author CMC sections of worldwide regulatory dossiers for clinical trials and marketing applications. In your role, you will gain understanding of how data from different functions within Product Development translates into regulatory content.

During your graduate programme, you will have the opportunity to:

• Learn about the coordination and preparation of small molecule and large molecule regulatory dossiers.
• Develop critical and analytical data and understand how data generated from other functional areas translates into regulatory dossiers.
• Learn about the importance of attention to detail when undertaking data verification of information withing filings.
• Interact with other critical functional areas such as drug product development, drug substance development, analytical testing and clinical supplies operations.  

What's on offer?

• The chance to join one of the top pharmaceutical companies where you can contribute to transforming patient's lives through science.
• The opportunity to embark on a unique role, with the ability to see all stages of a project and providing fantastic progression opportunities. 
• Great on-site benefits including an on-site gym, subsidised cafes and regular talks from various speakers.
• Social opportunities such as games nights, football teams, pride, family days and more. 
• Based in Moreton, under 20 minutes from Central Liverpool with hybrid working.
• A salary between £27k-30k 

What skills do I need?

• Degree (BSc or equivalent) in Biotechnology or a similar discipline.
• Excellent verbal and written communication skills with the ability to plan, organise and collaborate with other scientific disciplines effectively. 
• A higher degree (e.g. MSc, MChem, MPharm) and industry experience within a related environment is preferential, but not required. 

Wanting tips or advice on how to ace this application process? BMS are hosting a workshop on their advice for how you can make your application stand out. This will be taking place on the 13th March. Follow this link here to register: https://cvent.me/egwAlbrt=Acgzy4rrkWnedYt0a4qLg&locale=en&Refid=Student