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Senior Production Planner

CellaresSouth San Francisco, California, United StatesOnsite
This job is no longer open
We are seeking a highly motivated Senior Production Planner who will contribute significantly to the growth of Cellares and our mission to accelerate access to life-saving cell therapies. 
The primary focus of this position will be leading the planning and scheduling process for the Integrated Development Manufacturing Organization (IDMO) in South San Francisco.  As the Senior Production Planner, you will be responsible for facilitating and leading management of material planning, resource planning, demand planning, supply planning, supporting sales and operations planning (S&OP), and the master production schedule. The incumbent is responsible for setting goals and objectives that ensure overall integration of manufacturing and planning policies, processes, programs, and operational efficiencies for the IDMO.  This individual will have the highly impactful role of developing a world-class planning and scheduling process from the ground up.

Your strategy, processes, and planning skills will ensure operational success for the company. This is a multidisciplinary role and this individual will interface across many parts of the company (with MSAT, PD, AD, Operations, Materials Management, Quality, Facilities, and R&D) to develop the best plans and schedules possible. The successful candidate will be driven, motivated, and self-sufficient. The successful candidate should enjoy working in a fast-paced, mission-driven environment, and be prepared to tackle a broad selection of challenges as the company grows. You will also be able to quickly contribute and create structure, processes, planning and modeling tools from the ground up.

Responsibilities


  • Inventory Management: Leverage SAP, monitor inventory levels of raw materials, consumables, intermediates, and Finished Drug product to prevent shortages or overstock situations
  • Optimize inventory levels while considering factors like shelf life, lead times, and production schedules is essential
  • Production Planning: develop production schedules and plans based on demand forecasts, inventory levels, and manufacturing capacities
  • Coordinate with production teams to ensure timely manufacturing and availability of cell therapy products
  • Supply Chain Coordination: Collaborate with Procurement and Logistics teams, suppliers, distributors, and logistics partners to maintain an efficient supply chain to ensure timely delivery of critical materials and products
  • Process Improvement: Continuously review and optimize processes to improve efficiency, reduce costs, and enhance overall performance
  • Implement new technologies or methodologies to streamline operations
  • Compliance and Regulation: Ensure that all activities adhere to regulatory requirements and quality standards imposed by regulatory bodies like the FDA (Food and Drug Administration) or other relevant agencies
  • Maintain accurate records and documentation
  • Sales and Operations Planning: Key business partner for monthly S&OP including demand planning, supply/capacity planning, assumptions, reporting of actuals and KPIs

Requirements


  • 2+ years of experience in the cell therapy or related industry with experience in production planning/scheduling, supply chain, warehouse operations, and/or manufacturing operations
  • Strong understanding of ERP/MRP systems and processes (SAP is preferred)
  • Demonstrated ability to work cross-functionally and partner with other functional groups to achieve business objectives required
  • Skillful application of KPIs and metrics to manage business processes and support strong team performance
  • Cell/Gene Therapy and CDMO experience preferred
  • Knowledge of cGMP/GDP/Pharmaceutical regulations
  • Knowledge of Quality and Compliance systems
  • Must be able to manage shifting priorities to meet critical deadlines in a fast paced and dynamic, growing environment, while providing clear direction to team members
  • Excellent organizational and communication skills
  • Self-motivated and passionate about advancing the field of cell therapy
  • Self-awareness, integrity, authenticity, and a growth mindset

$90,000 - $210,000 a yearCellares total compensation package contains competitive base salaries, highly subsidized Medical, Dental, and Vision Plans, 401(k) Matching, Free EV Charging, Onsite lunches, and Stock options. All displayed pay ranges are approximate, negotiable, and location dependent.Apply for this job

This job is no longer open

Life at Cellares

Cellares is revolutionizing cell therapy manufacturing. We are developing a one-of-a-kind solution, The Cell Shuttle, to overcome the challenges associated with manufacturing so these life-saving therapies are affordable and widely available to patients who can benefit. The clinical impact of cell therapy in treating cancer has been proven, but this therapeutic approach has several limitations, especially in manufacturing, leaving extremely sick patients waiting for treatment and desperate for hope. Since cell therapy is currently produced for a single patient at a time, it is expensive to manufacture, requiring significant time and resources, and is difficult to scale. Preclinical and clinical scientists, as well as commercial cell therapy manufacturers also lack the options to fully automate their manufacturing process quickly, safely, cost-effectively and at the scale they need. The Cell Shuttle is an automated and closed end-to-end manufacturing solution that is flexible and scalable, enabling customers to run exact processes specified for their cell therapy. Compared with the current manual manufacturing processes for cell therapy, the Cell Shuttle’s next-generation automated manufacturing solution has 10 times the scalability (meaning 10 times more patient doses can be produced simultaneously), enables a three-fold reduction in process failure rates and will reduce the per-patient manufacturing cost by up to 70 percent for most processes.
Thrive Here & What We Value- Fastpaced, mission-driven environment- Collaborative and knowledge-sharing environment- Total patient demand for cell therapies at global scale- Industry 4.0 approach to mass manufacturing living drugs of the 21st century- Integrated Development and Manufacturing Organization (IDMO) with flexible, high-throughput platform- Accelerating access to life-saving cell therapies- WalkAway, end-to-end automation
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