Senior Specialist, Manufacturing Detailed Scheduler

4 weeks ago


Dublin, Dublin City, Ireland Bristol Myers Squibb Full time
Senior Specialist, Manufacturing Detailed Scheduler

Join to apply for the Senior Specialist, Manufacturing Detailed Scheduler role at Bristol Myers Squibb

Senior Specialist, Manufacturing Detailed Scheduler

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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.

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 .

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 on a Fixed Term Senior Specialist, Manufacturing Detailed Scheduler. Reporting to the Manager, Manufacturing Scheduler Planner, the ideal candidate will execute the detailed planning and scheduling for multiproduct manufacturing operations activities to ensure the safe and on-time delivery of manufactured drug substance products. The role will operate across functions to align key operations deliverables with network targets and planned output.

Key Duties And Responsibilities

  • Develop daily scheduling and assignment of activities in alignment with the Manufacturing schedule and priorities, with a Right First Time mindset.
  • Work with the Supply Chain organization, the Maintenance organization Planner, the 'New Product Introduction' programs and the Manufacturing Project Support Team, along with Sustaining Manufacturing on all aspects of batch planning to ensure alignment with high-level schedule
  • Develop detailed schedule scenarios for manufacturing activities, NPI's and Projects to manage plant and equipment conflicts and also operational capacity constraints.
  • Working directly with the Upstream operations manager, Downstream operations Manager and Manufacturing Projects Manager to endorse planning scenarios intended for the high-Level Schedule.
  • Working closely with Shift Manufacturing Leads to plan, assign and amend scheduled scenarios as required
  • Ensure coordination with Supply Chain to confirm raw materials and consumables are available for all planned work.
  • Ensure interaction with Reliability Maintenance team to ensure equipment is available for all planned work.
  • Review, plan and assign appropriate priority to facilitate stakeholder activities in the manufacturing schedule, to maximise efficiency and plant up-time
  • Maintaining a thorough knowledge of short-term and longer time business priorities and objectives through regular communication with leadership and other functions.

Qualifications, Knowledge and Skills Required:
  • A degree qualification in Science /Engineering or related discipline is preferred.
  • At least 5 years' experience in biopharmaceutical, pharmaceutical or medical device facility is required.
  • Strong communication, organizational and analytical skills are essential
  • Intermediate or advanced user skill of standard software applications eg. MS Word, MS Excel, Sharepoint.
  • Proficiency or working knowledge of scheduling software systems would be an advantage
  • Ability to work independently and also as part of a team.

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

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 a supportive culture, promoting global participation 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

Responsibilities

BMS has an 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.

Seniority level
  • Seniority levelAssociate
Employment type
  • Employment typeFull-time
Job function
  • Job functionManagement and Manufacturing
  • IndustriesPharmaceutical Manufacturing

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