Formulations Scientist

At Editas Medicine, we are pioneering the possible. Our mission and commitment is to translate the power and potential of the CRISPR/Cas12a and CRISPR/Cas9 genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world.  Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for a broad class of diseases.  

Why Choose Editas?

At Editas Medicine, we’re a team of courageous problem solvers, harnessing the power and potential of CRISPR gene editing to transform the future of medicine. Driven by a shared purpose to serve people living with serious diseases, we succeed together through collaboration, mutual respect, and innovation. If you want to be part of a team where your voice is heard and respected, where you can operate at the forefront of gene editing, and push the boundaries of what’s possible in medicine, come join us and...

US Remote (US East Coast Hours are required)

Essential Duties:

• Lead and execute the development of oral and sublingual formulations for peptides and other small molecules.
• Design and optimize formulations to improve drug stability, efficacy, and delivery.
• Review and interpret scientific literature to identify new approaches and innovative formulation strategies.
• Conduct formulation testing, stability studies, and analytical method development to support product development.
• Collaborate with cross-functional teams including process development, analytical, and manufacturing to ensure smooth project progression.
• Document and present formulation development findings and progress reports to stakeholders.
• Maintain up-to-date knowledge of current trends, advancements, and best practices in the field of formulation science.
...

US Remote (US East Coast Hours are required)

Essential Duties:

• Lead and execute the development of oral and sublingual formulations for peptides and other small molecules.
• Design and optimize formulations to improve drug stability, efficacy, and delivery.
• Review and interpret scientific literature to identify new approaches and innovative formulation strategies.
• Conduct formulation testing, stability studies, and analytical method development to support product development.
• Collaborate with cross-functional teams including process development, analytical, and manufacturing to ensure smooth project progression.
• Document and present formulation development findings and progress reports to stakeholders.
• Maintain up-to-date knowledge of current trends, advancements, and best practices in the field of formulation science.
...

Job Title: Senior Scientist/Principal Scientist, Formulation Development

Department: Formulation Development

Reporting To: Director, Pharmaceutics

Classification: Exempt

Salary Range: $110,000-$155,000/yr, depending on experience

What We Do

BioDuro-Sundia is one of the premier Contract Research, Development and Manufacturing Organizations (CRDMO) globally, with more than 2,200 employees.  Our US operations are US headquartered in Irvine, CA. Our 7 global facilities provide integrated solutions and exceptional services to our clientele for challenging preclinical and clinical trial projects. With capabilities spanning Drug Discovery, Development, and Manufacturing, it is no surprise that BioDuro-Sundia is a leading partner of choice.

Why BioDuro-Sundia?

Take the...

HYBRID with at least 3x/office/week in Malvern, PA is REQUIRED.

Essential Duties:

• Lead and execute the development of oral and sublingual formulations for peptides and other small molecules.
• Design and optimize formulations to improve drug stability, efficacy, and delivery.
• Review and interpret scientific literature to identify new approaches and innovative formulation strategies.
• Conduct formulation testing, stability studies, and analytical method development to support product development.
• Collaborate with cross-functional teams including process development, analytical, and manufacturing to ensure smooth project progression.
• Document and present formulation development findings and progress reports to stakeholders.
• Maintain up-to-date knowledge of current trends, advancements, and best practices in the field of...

At Editas, we’re driven by a collective purpose, to bring transformative and life changing therapies to people living with serious diseases with the greatest unmet needs. This fuels our drive to excel in scientific innovation, allowing us to harness the power and potential of CRISPR/Cas9 and CRISPR/Cpf1 (Cas12a) gene editing.

We believe our people are at the core of everything we do, and we’re committed to cultivating a culture where every individual feels valued and included. To do this, we strive to integrate belonging, inclusivity, diversity, and equity into every aspect of our organization.

Together, we are leading the way towards a healthier and more equitable future.

Position Summary

The Delivery and Editing Technologies Team optimizes current and new editing and delivery technology formats to provide the best in vivo delivery and gene editing solutions for current and future therapeutic programs and is looking to add highly...

Job Title: Scientist I, Formulation Development

Department: Formulation Development

Reporting To: Director, Formulation Development

Classification: Exempt

 Range: 80k-97k

What We Do

BioDuro-Sundia is one of the premier Contract Research, Development and Manufacturing Organizations (CRDMO) globally, with more than 2,200 employees.  Our US operations are US headquartered in Irvine, CA. Our 7 global facilities provide integrated solutions and exceptional services to our clientele for challenging preclinical and clinical trial projects. With capabilities spanning Drug Discovery, Development, and Manufacturing, it is no surprise that BioDuro-Sundia is a leading partner of choice.

Why BioDuro-Sundia?

Take the next step in your career and join BioDuro-Sundia today to change lives through the products we...

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