Specialist, Upstream Manufacturing

at  BristolMyers Squibb

WORKING WITH US

Challenging. Meaningful. Life-changing. Those aren’t words that are usually associated with a job. But working at Bristol Myers Squibb is anything but usual. Here, uniquely interesting work happens every day, in every department. From optimizing a production line to the latest breakthroughs in cell therapy, this is work that transforms the lives of patients, and the careers of those who do it. You’ll get the chance to grow and thrive through opportunities uncommon in scale and scope, alongside high-achieving teams rich in diversity. Take your career farther than you thought possible.
Bristol Myers Squibb recognizes the importance of balance and flexibility in our work environment. We offer a wide variety of competitive benefits, services and programs that provide our employees with the resources to pursue their goals, both at work and in their personal lives. Read more: careers.bms.com/working-with-us .

BMS Cruiserath Biologics is seeking to recruit a 12 month fixed term contract Upstream Bioprocess Associate within the Manufacturing Operations group. Reporting to the Shift Lead, the Upstream Bioprocess Associate will support the ongoing manufacturing operations within the facility, as well as commissioning and qualification activities for the process equipment. This is a 12/7 and/or 24/7 shift role

A typical day might include the following:

• Execution of commercial manufacturing processes according to established work instructions
• Creation and update of operating procedures & other relevant documentation for large scale manufacturing
• Operating production equipment within the assigned functional area
• Adhering to Good Manufacturing Practices and Standard Operating Procedures
• Taking part in investigations and optimisation of processes using scientific, engineering and lean principles
• Proficient use of process automation systems (i.e. Delta V and Syncade Interactions, OSI/Pi Historian) and some supporting business systems (i.e. SAP, Infinity, Maximo etc.)
• Assisting with review of batch and exception reports for manufacturing lots in conjunction with Quality Assurance representative and provide input to related investigations and QA audit activities
• Working with the manufacturing operations group, the project design team, the CQV team, & the Automation/Computer Systems Validation teams to facilitate the implementation of the project design, validation and operation of the MPCC manufacturing facility
• Engaging in and supporting a culture of continuous improvement and operational excellence through ownership of improvement for work processes, equipment, and a safe working environment

This job might be for you if:

• You possess a minimum of Level 6 qualification in an Engineering/Science related discipline; however, relevant experience in a similar regulated industry will also be considered (e.g. cGMP, ISO or similar cleanroom industry experience strongly preferred)
• You have 3+ years’ working experience in a large-scale biopharmaceutical manufacturing facility
• You have experience with Delta V and MES or similar control and data acquisition systems
• You can demonstrate an ability to work independently and as part of a team.
• You have a demonstrated problem-solving ability and the ability to adhere to scheduled timelines
• You have excellent communication skills and the ability to work in a cross-functional, collaborative, and fast-paced environment.

Due to the nature of the manufacturing role, shift work will be required as the site operates a 24/7mode of operations.

Why you should apply

• You will help patients in their fight against serious diseases
• You will be part of a company that encourages excellence and innovation, respects diversity, develops leaders and values its employees.
• You’ll get a competitive salary and a great benefits package including an annual bonus, pension contribution, family medical allowance, life assurance and on-site gym