Manager, Upstream Manufacturing Technical Lead

3 weeks ago

County Dublin, Ireland Bristol Myers Squibb Full time

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 Ireland

Bristol Myers Squibb has been in operation in Ireland since 1964, employing over 650 people across a range of activities and business units

Located in Dublin, Cruiserath Biologics Campus, a one billion Multi-Product Cell Culture Biologics Manufacturing facility plays a central role in the Global Product Development and Supply (GPS) network as the company's first European biologics manufacturing facility. This state of the art facility will produce multiple therapies for the company's growing biologics portfolio. Global Biologics Laboratory (GBL) responsible for the release testing of Biologics Drug product for the network, is also based on the Cruiserath Biologics Campus.

BMS Cruiserath has been awarded "Biopharma Company of the Year 2019" in the Irish Pharma Industry Awards and is certified as a Great Place to Work since 2017, including as a Great Place to Work for Women in 2020, 2021 and 2022.

The Role

BMS Cruiserath Biologics is seeking to recruit an Upstream Technical Lead within the Manufacturing Operations group. The Technical Lead will support Upstream Manufacturing activities and also be a key role in investigation resolution.

This is a 24/7 shift role.

Key Duties and Responsibilities:

Manufacturing SME for technical issue trouble shooting/resolution during/post start-up. Provide expertise and training to Bioprocess Associates in relation to the day to day operations. Working with the cross functional departments to facilitate the implementation of the project design and validation of the MPCC manufacturing facility. Working with Bioprocess Associates to generate the Procedures & Training documentation required to enable Manufacturing to start-up and complete training on time. Work in conjunction with the Shift Lead to establish and lead a team of Bioprocess Associates within the Multi Product Cell Culture facility. Assist in the execution of commercial manufacturing processes according to established electronic work instructions and production records. Support and lead key meetings on behalf of Operations. Lead and implement Lean Manufacturing principles. Support process related investigations and QA audit activities. Creating and approving operating procedures. Lead operational readiness activities.

Qualifications, Knowledge and Skills Required:

The candidate will hold a minimum BSc. or B.Eng qualification. At least 3 years' experience in a GMP manufacturing environment with at least 1 years' experience in Upstream Manufacturing within the Biologics drug substance operations A history of functional and operational accomplishments is essential A Good understanding of systems such as Delta V and SAP is required The successful candidate will be a proven subject matter expert in relation to Upstream Biologics processes and have a proven ability to lead a team of Bioprocess Associates.

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, 27 days of annual leave, life assurance and on-site gym

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