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.

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 and 2021.  

For more information about Bristol Myers Squibb, visit us at BMS.com/ie

The Role

BMS Cruiserath Biologics is seeking to recruit a permanent Manufacturing Engineer.
Reporting to the Downstream Senior Manufacturing Engineering Manager, the
Manufacturing Engineer will be the System Owner for Downstream Process Equipment
providing engineering support for Manufacturing systems and equipment.
 

Key Duties and Responsibilities:

Support for Downstream Manufacturing Equipment performance within the Multi-Product Cell Culture (MPCC) building.Engineering owner for specific manufacturing areas and systems, focused on acquiring an in-depth knowledge of process design and equipment operation to support Manufacturing, Maintenance, Quality, and Automation.Primary System Engineer for Column Pack and UFDF Unit Operations.Provide support to Manufacturing Operations on troubleshooting equipment, process, and automation issues.Supporting/leading manufacturing/process equipment investigations and continuous improvement projects.Ensuring system compliance with all Regulatory requirements including Quality (cGDP/GMP’s), and EHS requirements & procedures.Supporting internal and external audits as the Manufacturing Engineering Technical resource.Responsible for Clean in Place (CIP), Sanitisations and Steam in Place (SIP) changes, optimisations, and performance.

Accountable for redlining, reviewing, and approving of Automation Design Specifications in support to implementation of software changes to the Process Automation System (PAS).Manufacturing engineering equipment lead for new product introduction with support for equipment capability assessments, new equipment requirements and recipe design.Develop goals into appropriate scope and deliverables with demonstrated ability to meet agreed timelines.  Plan and execute work assignments with ability to interpret results and report out to peers and stakeholders.Have a systematic approach to completing work activities, be willing to take on new activities, look to improve and contribute to building a sense of purpose within the team.Champion the use of new methods/technologies, continuous improvement, and data analytics (OSI PI and SEEQ).

Qualifications, Knowledge and Skills Required:

The successful candidate will preferably have a BS in Engineering (Chemical, Bioprocessing or Mechanical preferred) with 2-3 years plus experience (or equivalent) with manufacturing equipment support in the Biotechnology manufacturing industry.Understanding of process design, construction, and qualification in accordance with Bio-Pharmaceutical Engineering principles.Knowledgeable and experienced in engineering principles related to typical biopharmaceutical downstream processing and support equipment including, but not limited to, Filtration, CIP, SIP, and Chromatography.Candidates must be effective in both a team environment and an individual contributor role with minimal supervision.Ability to work extended hours or a modified work schedule as required for coverage of 24/7 manufacturing operation.  The position is Monday through Friday, first shift, but requires on-call availability.The job requires levels of technical knowledge, and the candidate should have the ability to proactively troubleshoot.Knowledge of Delta V, or other process automation software required; ability to use process historian and analyze data to assist troubleshooting.

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, but not only, an annual bonus, pension contribution, family health insurance, 27 days annual leave, access to BMS Cruiserath on-site gym and life assurance.

BMSBL

#LI-Hybrid

If you come across a role that intrigues you but doesn’t perfectly line up with your resume, we encourage you to apply anyway. You could be one step away from work that will transform your life and career.

Uniquely Interesting Work, Life-changing Careers
With a single vision as inspiring as “Transforming patients’ lives through science™ ”, every BMS employee plays an integral role in work that goes far beyond ordinary. Each of us is empowered to apply our individual talents and unique perspectives in an inclusive culture, promoting diversity in clinical trials, while our shared values of passion, innovation, urgency, accountability, inclusion and integrity bring out the highest potential of each of our colleagues.

On-site Protocol

BMS has a diverse occupancy structure that determines where an employee is required to conduct their work. This structure includes site-essential, site-by-design, field-based and remote-by-design jobs. The occupancy type that you are assigned is determined by the nature and responsibilities of your role:

Site-essential roles require 100% of shifts onsite at your assigned facility. Site-by-design roles may be eligible for a hybrid work model with at least 50% onsite at your assigned facility. For these roles, onsite presence is considered an essential job function and is critical to collaboration, innovation, productivity, and a positive Company culture. For field-based and remote-by-design roles the ability to physically travel to visit customers, patients or business partners and to attend meetings on behalf of BMS as directed is an essential job function.

BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles. Applicants can request a reasonable workplace accommodation/adjustment prior to accepting a job offer. If you require reasonable accommodations/adjustments in completing this application, or in any part of the recruitment process, direct your inquiries to adastaffingsupport@bms.com. Visit careers.bms.com/eeo-accessibility to access our complete Equal Employment Opportunity statement.

BMS cares about your well-being and the well-being of our staff, customers, patients, and communities. As a result, the Company strongly recommends that all employees be fully vaccinated for Covid-19 and keep up to date with Covid-19 boosters.

BMS will consider for employment qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.

If you live in or expect to work from Los Angeles County if hired for this position, please visit this page for important additional information: https://careers.bms.com/california-residents/

Any data processed in connection with role applications will be treated in accordance with applicable data privacy policies and regulations.