Support the execution of one or more processes that include Formulation, Filling (vial & syringe), Lyophilization, Capping, Visual Inspection & Primary Packaging
Support technical issue troubleshooting, resolution both during and post facility start-up.
Work with the cross functional departments to facilitate the implementation of the project design and validation of the SDP manufacturing facility.
Support all phases of Commissioning / Qualification and Validation during Start-up phase of state-of-the-art Drug Product Facility
Support all Capital / Tech Transfer / Operational Readiness activities to support Commercial Readiness
Support delivery of training to SDP team on day-to-day operations within area of responsibility
Right First-Time execution of commercial manufacturing processes according to established work instructions
Support the implementation of all key Operational Excellence initiatives (5S / Std Work / LSW / Kaizen / Problem Solving etc.)
Taking part in investigations and optimization of processes using scientific, engineering and lean principles
Proficient use of process automation systems
Assisting with review of batch and exception reports for manufacturing lots in conjunction with Quality Assurance representative
Engages in and supports culture of continuous improvement initiatives and safe working practices.
Designee for Senior DPA as required.
Support any other business deliverables as needed.
Qualifications & Experience
Experience in a high-speed manufacturing / regulated environment essential
Qualification in science, engineering, or related subject desirable.
Expertise in sterile drug product manufacturing along with demonstrated proficiency in technical troubleshooting and resolution is advantageous but not essential.
Ability to flexibly adapt to changing business needs in a start-up environment.
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
#LI-Onsite
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
Benefits
Vision insurancePerformance bonus
Additional Information
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. 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 Sterile Drug Product is seeking an experienced individual with manufacturing experience to provide on the floor technical support to our manufacturing teams within our new Sterile Drug Product (SDP) facility.
Reporting to the Senior Manager, Manufacturing Shift Lead, the Drug Product Associate will play a key role in the establishing our multi-product commercial Drug Product Facility with both vial and syringe fill finish technology. The Drug Product Associate will provide input and support all phases of the SDP project, such as, CQV, Site Operational Readiness, Technical Transfer, new product introduction and commercialization activities. Post start-up this role will be embedded within the shift teams charged with delivering the manufacturing plan for the facility.
The start-up nature of this project will require adaptability & innovation due to the multiple project phases and multiple products onsite. The role will be both challenging & rewarding and will thus ensure that the successful candidate can seize a wide range of development opportunities within BMS.
The position will commence on a day schedule, with a planned transition to shift work in the future
Bristol-myers Squibb · Cruiserath -, Ireland