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Solid Biosciences

Manufacturing Project Coordinator

301 - Manufacturing – Cambridge, Massachusetts
Department 301 - Manufacturing
Employment Type Full-Time
Minimum Experience Mid-level


In this new role for Solid you will be responsible for the coordination of manufacturing and MS&T projects. Support the manufacturing team through maintenance of internal and external schedules, resources, budgets, and meetings ensuring that the team is on time and on budget.

To be successful as a Project Coordinator, candidate will need to be able to work on tight deadlines, be competent in using Microsoft Office applications such as Word and Excel, and have exceptional verbal, written, and presentation skills

Key Duties & Accountabilities:

  • Assist in the planning and execution of manufacturing projects and production runs while adhering to budget, scope, and schedule requirements 
  • Helps ensure consistent practices throughout all phases of the project and production life cycle 
  • Organize, attend, and participate in stakeholder meetings
  • Execute high quality, integrated, cross-functional project plans 
  •  Applies best practices in the development, initiation, planning, execution, control, and shutdown of projects
  • Facilitate meetings where appropriate, and distribute minutes to all project team members
  • Document and follow up on important actions and decisions from meetings.
  • Provide administrative support as needed
  • Interact with process development, quality assurance, quality control, and regulatory teams
  • Publish reports and present to leadership as appropriate
  • Management of Solid GMP inventory including critical raw materials
  • Perform of other related duties and ad hoc projects as required by position

Competencies Required:

  • Project Management
  • Attention to Detail
  • Organization
  • Communication – oral, written, & presentation
  • Ability to work with changing priorities in a dynamic environment
  • Knowledge of MS Office suite and the ability to learn additional software as required
  • Proficiency in MS Project and MS Visio

Knowledge: Education, Experience, & Skills:

  • BS degree in biology or related field required
  • 3+ years’ experience with GMP production
  • Familiarity with FDA regulations and Quality Assurance a plus
  • Strong organizational skills and attention to detail, including the ability to handle a variety of tasks in a fast-paced environment
  • Excellent written, and oral communication skills required
  • Proficiency in database management and software implementation preferred

Travel Commitment:

  • Manufacturing Project Coordinator
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  • Location
    Cambridge, Massachusetts
  • Department
    301 - Manufacturing
  • Employment Type
  • Minimum Experience
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