R&D OPS - Associate Specialist, Production Planning and Scheduling
Listed on 2026-07-01
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Manufacturing / Production
Manufacturing & Industrial Operations, Quality Engineering
Associate Specialist, Production Planning And Scheduling
Location:
Bothell, WA
Top
Skills:
- ERP experience
- Experience in GMP or regulated environment
- Strong computer skills with Microsoft Office
- Strong communication skills both written and oral.
- Knowledge of Manufacturing, Operations and Inventory Control
- Cross Functional Collaboration experience
Plans and schedules production related activities at the cell therapy manufacturing facility. Provides manufacturing operations with a plan that maximizes efficiency, resources, and capacity. Achieves on time delivery within budget. Work on projects/matters of moderate complexity. Evaluates and develops scheduling tools and provides technical expertise.
Required Competencies:
Education:
Bachelor's Degree in relevant science, engineering or similar discipline preferred.
Experience:
3-6 years preferred; 2+ years of scheduling experience in cGMP manufacturing environment desired. Experience in scheduling cell therapy manufacturing preferred. Experience in material planning and/or finite scheduling in a medium to high volume environment, knowledge of scheduling platforms preferred.
Duties And Responsibilities:
- Plans and schedules production schedules to meet product demand at the site.
- Plan and schedule all associated production and support activities including intermediates, product shipment, facility and equipment maintenance.
- Work with QA, QC and Material Management to ensure raw materials are tested, released, and available to support all manufacturing and support activities.
- Work with Document Control to ensure all documents (i.e. batch records and packaging records) are ready for Manufacturing.
- Build strong relationships and communication with all functions.
- Provide exceptional customer service.
- Advanced knowledge of forecasting, capacity planning, and production planning.
- Knowledge of cGMP regulations and FDA guidance applicable to biologics and cell therapy (or related) manufacturing.
- Ability to work independently on projects or problems of moderate scope to meet objectives. Troubleshoots and identifies causes and suggests solutions.
- Attention to detail and ability to perform with a high degree of accuracy.
- Source of imaginative, thorough, and innovative solutions to a wide range of difficult problems.
- Exhibits leadership behaviors including collaborating for results and developing/executing strategy.
- May serve as a resource to more junior members of the team.
- Experience in lean, operational excellence, six sigma, or continuous improvement, and process mapping preferred. Supports an environment that encourages continuous improvement, best practices and appropriate risk taking.
- Ability to influence key stakeholders of internal and external teams.
- Excellent communication and presentation skills as well as the ability to effectively communicate across all levels of the company.
- Strong analytical and problem-solving abilities.
- Expert in Microsoft Office programs.
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