- Establish robust operational readiness plans to transition to full-scale production,
- Develop and execute a project quality plan with audit readiness components,
- Lead the hiring, training, and development of a high-performing Quality Operations team,
- Collaborate with cross-functional teams in a matrixed environment,
- Drive continuous improvement initiatives and operational efficiency,
- Bachelor of Science degree in relevant field,
- Minimum 8 years of experience in aseptic drug product manufacturing,
- Strong leadership and project management skills,
- Excellent knowledge of cGMP regulations and cleanroom operations,
- Ability to work cross-functionally and manage complex projects,
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BioSpace, Inc. Norwood, United StatesJob Details The Role As the Director of Drug Product Operations (Formulation and Filling) at Moderna, you have a key leadership role responsible for overseeing the formulation and filling of aseptically manufactured drug products at a new state-of-the-art Drug Product (Fill Finis ...
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Modernatx Norwood, United StatesTheRoleReporting to the Sr. Director of Sterility Assurance, the Associate Director of Sterility Assurance is tasked with leading the development and management of an aseptic and sterility assurance program for a state-of-the-art Drug Product (Fill Finish) cGMP manufacturing faci ...
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BioSpace, Inc. Norwood, United StatesJob Details · The Role · Reporting to the Sr. Director of Sterility Assurance, the Associate Director of Sterility Assurance is tasked with leading the development and management of an aseptic and sterility assurance program for a state-of-the-art Drug Product (Fill Finish) cGM ...
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Moderna, Inc. Norwood, United States Full timeThe Role · Reporting to the Director, QA Drug Product, the Associate Director, QA Operations is responsible for leading the quality and compliance readiness for a state-of-the-art Drug Product (Fill Finish) cGMP manufacturing facility. This role involves ensuring operational read ...
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Moderna, Inc. Norwood, United States Full timeThe Role · The Manufacturing Operations Support team is responsible for the day-to-day operational support of clinical and commercial drug substance processing and release through batch record review and continuous improvement projects. A Sr. Technical Specialist, Manufacturing u ...
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Moderna, Inc. Norwood, United States Full timeThe Role · Reporting to the Sr. Director of Sterility Assurance, the Associate Director of Sterility Assurance is tasked with leading the development and management of an aseptic and sterility assurance program for a state-of-the-art Drug Product (Fill Finish) cGMP manufacturing ...
Associate Director, QA Operations, Drug Product - Norwood, United States - Moderna Theraputics
Description
Job Title: Associate Director, QA Operations at Moderna
Company: Moderna
The Associate Director, QA Operations at Moderna plays a crucial role in overseeing the quality and compliance readiness for a cutting-edge Drug Product manufacturing facility. In this role, you'll be leading the operational readiness for the production of clinical and commercial drug products, ensuring adherence to industry best practices and regulatory standards.
Here's the breakdown of what you'll be doing:
To qualify for this role, you'll need:
If you're ready to make an impact in a high-growth environment, Moderna offers a comprehensive benefits package including medical, dental, vision coverage, flexible spending accounts, family care benefits, paid time off, and more. Join us in our mission to revolutionize medicine and change the world. Apply now!