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Magenta Therapetuics
Cambridge, Massachusetts, United States
12 days ago
Frederick National Laboratory
Frederick, MD, US
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Brooks Automation
Chelmsford, MA, US
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Magenta Therapetuics
Cambridge, Massachusetts, United States
12 days ago

Description

Are you looking for a role with impact?

Magenta Therapeutics is a clinical-stage biotechnology company developing therapeutics to reset the immune system to cure more patients with devastating and life-threatening diseases. This immune reset approach can be applied through stem cell transplant to multiple diseases, including autoimmune diseases, such as multiple sclerosis and systemic sclerosis; blood cancers, such as acute myeloid leukemia; and genetic diseases, such as sickle cell disease.

Magenta’s comprehensive approach to precision immune system reset will transform many aspects of the transplant process, aiming to make it safer and more effective.  Our culture is fueled by a driven, passionate group of people committed to making a difference, seizing opportunities for maximum impact, and pursuing progress for the patients we seek to serve.

We are seeking an experienced leader to head our on-going pre-clinical and clinical manufacturing efforts of drug product development and manufacturing across our entire multi–modality portfolio.  We are seeking someone that is highly motivated to help Magenta therapeutics successfully navigate the challenges drug product development and manufacturing from pre-clinical through phase 3 and post commercialization.  The incumbent will report to the Chief Technical Officer and will be responsible for development and execution of all areas related to the successful drug product development, manufacturing, and filing.  Our team is a place where the autonomy to chase an idea and drive innovative solutions are not just encouraged and supported but expected. If you are looking for a place where you can impact the strategy of your company while remaining involved with the technical data-driven day to day decisions, we would like to hear from you.

You are perfect for this role if you are engaged by and want to be responsible for:

  • Support the development and oversight of drug product process and manufacturing and eventual commercial manufacturing across multiple modalities.
  • Ability to provide technical oversight of CMDOs through batch record review, and PIP.
  • Own process validation-related quality systems (CAPA, Change Control)

We would be thrilled if you brought the following with you:

  • Advanced degree in a relevant scientific discipline with at least 5 years of industry experience in drug product manufacturing and development.
  • Experience working with external CDMOs
  • Experience in both ADCs and large peptides

Successful leaders and contributors within Magenta are: 

  • Driven.  You will be focused on the achievement of Magenta’s mission and major corporate goals.
  • Results-focused.  Demonstrated record of exceeding stretch goals, and willing to bring creative problem-solving skills to challenges along the way
  • Intuitive. You will enjoy learning and being involved in the content of our whole business, thriving on a very fast-paced and growing business
  • Collaborative.  You will have demonstrated the ability to achieve objectives across complex projects and organizational structures
  • Process-oriented, yet flexible. You will appreciate and be able to create and drive process, while also recognizing when flexibility is needed.
  • Transparent and Articulate.  You will have the ability to communicate clearly and concisely with all stakeholders
  • Independent. You will be able to self-organize and operate effectively without significant day-to-day oversight, while staying tightly connected to key leaders and teams across the company
  • A role model for the company’s cultural pillars; Courage, Commitment & Excellence

At Magenta, we celebrate our differences. We value the power of a diverse array of folks who bring all of themselves to their work. We embrace cultural, cognitive, social, and professional diversity because we know the only way we’re going to make new cures possible is by working together.



Job Information

  • Job ID: 58137233
  • Location:
    Cambridge, Massachusetts, United States
  • Position Title: Associate Director/Director, Drug Product Development and Manufacturing
  • Company Name: Magenta Therapetuics
  • Job Function: Drug Development,
    Manufacturing,
    Scientist
  • Job Type: Full-Time
Biotechnology

Headquartered in Cambridge, Mass., Magenta Therapeutics (Nasdaq:MGTA) is a clinical-stage biotechnology company developing therapeutics to reset the immune system in order to cure more patients with devastating and life-threatening diseases. This immune reset approach can be applied through stem cell transplant to multiple diseases, including autoimmune diseases, such as multiple sclerosis and systemic sclerosis; blood cancers, such as acute myeloid leukemia; and genetic diseases, such as sickle cell disease. Magenta’s compr...

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