Manager, Manufacturing Scheduler Planner
Bristol-Myers Squibb operates a state-of-the-art multi-product biologics manufacturing facility in Cruiserath, Dublin 15. The facility is a key part of BMS’s global biologics manufacturing network.
We are seeking a permanent Manufacturing Planner to lead a team of Detailed Manufacturing Schedulers and cultivate strong cross‑functional partnerships with key stakeholders, including Supply Chain, Engineering, Project Management, Maintenance Planning, New Product Introduction (NPI) programs, and Sustainability teams.
Key Responsibilities
Leading and overseeing a team of Detailed Manufacturing Schedulers to ensure effective coordination and execution of production plans.
Own and facilitate the daily production meeting, ensuring effective coordination among all attending stakeholders and alignment on operational priorities in the MPCC.
Collaborate with all stakeholders including the Supply Chain organization, Maintenance Planning, NPI programs, the Manufacturing Project Support Team, and Sustaining Manufacturing to ensure comprehensive alignment of batch planning activities with the overarching production schedule.
Develop comprehensive scheduling scenarios for manufacturing operations, NPIs, and strategic projects to proactively manage equipment utilization conflicts and address operational capacity constraints.
Take ownership of annual costing and spend tracking for Kanban materials used within the MPCC facility and provide weekly updates to stakeholders during the Manufacturing Tier 2 meeting.
Partner directly with the Upstream Operations Manager, Downstream Operations Manager, and Manufacturing Projects Manager to validate and endorse planning scenarios for integration into the high‑level production schedule.
Collaborate closely with Shift Manufacturing Leads to plan, assign, and adjust scheduling scenarios as needed to support dynamic production requirements.
Ensure that Detailed Manufacturing Schedulers coordinate effectively with the Supply Chain team to verify the availability of raw materials and consumables for all scheduled production activities.
Partner with the Manufacturing Technical Training team and shift managers to ensure smooth and effective onboarding experiences, including comprehensive "door‑to‑floor" training for new hires.
Ensure that Detailed Manufacturing Schedulers maintain close coordination with the Reliability Maintenance team to confirm equipment readiness for all scheduled production activities.
Review, prioritize, and assign stakeholder activities within the manufacturing schedule to optimize operational efficiency and maximize plant uptime.
Maintain a strong understanding of both short‑term priorities and long‑term business objectives through consistent engagement with leadership and cross‑functional teams.
Demonstrate proficiency in all scheduling software utilized on site, including Excel, Bio‑G, Kinaxis, and other relevant planning tools, to support efficient and accurate production scheduling.
Coach and mentor the Detailed Manufacturing Scheduling team to foster continuous development, ensure future success, and support succession planning initiatives.
Requirements
A degree qualification in Science, Engineering, or related discipline is preferred.
At least 5 years’ experience in a 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 (e.g., MS Word, MS Excel, SharePoint).
Proficiency or working knowledge of scheduling software systems would be an advantage.
Ability to work independently and 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 receive 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.
On‑Site Protocol
Site‑essential roles require 100% of shifts onsite at the assigned facility. BMS is committed 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 accommodation prior to accepting a job offer.
All employees are strongly recommended to be fully vaccinated for Covid‑19 and keep up‑to‑date with Covid‑19 boosters. BMS will consider qualified applicants with arrest and conviction records, pursuant to applicable laws in your area.
Equal Opportunity Employment
BMS is an equal opportunity employer and encourages applications from all backgrounds. For our complete Equal Employment Opportunity statement, visit careers.bms.com/eeo‑accessibility.
Location & Compensation
Dublin, County Dublin, Ireland
€70,000.00 – €75,000.00 per year (subject to change)
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