Planner, Global Planning

Alnylam Pharmaceuticals • Cambridge, MA

1d • Hybrid

About The Position

The Global Planning Planner is a member of the Supply Chain organization responsible for the planning and oversight of Drug Substance and Drug Product manufacturing for the early-stage pipeline, focusing primarily on pre-clinical and phase 1 programs. This position works closely with key stakeholders including Program Teams, Process Sciences, CMC, Internal and External Manufacturing, Quality Assurance, Regulatory Affairs and Supply Chain to ensure seamless supply of Clinical Trial Material. A successful candidate will be skilled at understanding Supply and Operations Planning Process and the challenges/timelines of early-stage development. They will excel in a collaborative work environment and exhibit strong attention to detail and the strong ability to manage multiple priorities. Reporting to the Associate Director of early-stage global planning, you'll be tasked with maintaining and developing complex planning strategies, while also leveraging SAP and other ERP planning systems.
This position is hybrid and will be primarily located in Cambridge, MA.

Requirements

• B.S. in Business, Supply Chain, Engineering or science-related discipline.
• A minimum 2 years of relevant experience in a Manufacturing or Supply Chain role with experience in Production, Planning, or Scheduling.
• Excellent math and computer skills required, including Microsoft Office/Excel/PowerPoint.
• Good knowledge of computerized production and inventory control systems (SAP) and documentation practices.
• Demonstrated ability to manage multiple priorities against ambitious timelines. Strong project management ability.
• Attention to detail and ability to perform with a high degree of accuracy
• Ability to work independently on projects or problems of short-term scope to meet objectives. Troubleshoots and identifies causes and suggests solutions
• Exceptional communication skills and ability to communicate to multiple levels within company.
• Strong problem-solving skills and ability to work cross-functionally as critical member of site team.
• Solid understanding of pharmaceutical manufacturing processes, GMP principles, and new product introduction.

Nice To Haves

• ERP planning experience a plus.
• Relevant industry certifications are a plus (APICS CSCP/CPIM).

Responsibilities

• Supports Early-Stage Clinical Supply and Operations Planning Process (CS&OP)
• Collaborate with external partners to ensure drug substance and drug product supply needs are met in line with contractual obligations
• Partner with CMC, Process Sciences, Program Team, QA, QC, Finance and Material Management to ensure material availability in line with clinical program timelines and budget
• Execute planning and procurement activities based on manufacturing schedules and Material Requirements Planning (MRP) principles
• Maintain and update master data entry as directed
• Set and maintain safety stock and replenishment strategies for production materials
• Works Cross Functionally to Develop Scenario Plans and Strategies that result in production plans that meet program, capacity and budget requirements
• Develops annual long range manufacturing plans based on available information, highlighting areas of constraint
• Supports annual budget review to ensure manufacturing plans are timely and accurate for financial planning purposes.

Benefits

• comprehensive benefits including medical, dental, and vision coverage, life and disability insurance, a lifestyle reimbursement program, flexible spending and health savings accounts and a 401(k)with a generous company match
• Eligible employees enjoy paid time off, wellness days, holidays, and two company-wide recharge breaks.
• We also offer generous family resources and leave.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level