Production Planning and Scheduling Associate W/GMP

Bothell, WA

Posted: 08/01/2022 Job Number: 21316730

Job Description

PRODUCTION PLANNING AND SCHEDULING ASSOCIATE W/GMP
BOTHELL, WA
Required Skills:
  • Bachelor's Degree in relevant science, engineering or similar discipline preferred.
  • 2+ years of scheduling experience in cGMP manufacturing environment desired; 3-6 years preferred.
  • 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.
  • Ability to work independently on projects or problems of moderate scope to meet objectives.
  • Attention to detail and ability to perform with a high degree of accuracy.
  • Exhibits leadership behaviors including collaborating for results and developing/executing strategy.
  • Experience in lean, operational excellence, six sigma, or continuous improvement, and process mapping preferred.
  • 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.

Project Description:
  • 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.
  • 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.
  • Troubleshoots and identifies causes and suggests solutions.
  • Source of imaginative, thorough, and innovative solutions to a wide range of difficult problems.
  • May serve as a resource to more junior members of the team.
  • Supports an environment that encourages continuous improvement, best practices and appropriate risk taking.

This 12+ month position starts ASAP.

Please E-MAIL your resume (attachment to email) with rate and availability to Cindi: cindi@alphaconsulting.Com

ALPHA'S REQUIREMENT #22-02303
MUST BE ELIGIBLE TO WORK IN THE U.S. AS AN HOURLY W2 EMPLOYEE

Meet Your Recruiter

Cindi Pisnoy

Apply Online

Send an email reminder to:

Refer A Friend

Share This Job:

Related Jobs:

Login to save this search and get notified of similar positions.