Oruka Therapeutics logoOruka Therapeutics logo

Associate Director, Downstream, Manufacturing Sciences and Technology (Biologics)

Oruka TherapeuticsWaltham, Massachusetts, United States
Hybrid Full-time $175K/yr - $200K/yr

Clicking Apply Now takes you to AutoApply where you can tailor your resume and apply.


Experience Level

Senior Level Manager

Qualifications

Key Responsibilities:Oversee the transfer of manufacturing processes from late-stage development to large-scale production at contract development and manufacturing organizations (CDMOs) across multiple programs. Collaborate with CDMOs to identify gaps and implement enhancements to optimize processes.

About the job

About Us:

Oruka Therapeutics (Nasdaq: ORKA) is at the forefront of developing innovative biologics aimed at revolutionizing the treatment of chronic skin disorders. Our mission is to empower patients suffering from conditions such as plaque psoriasis by providing opportunities for significant disease clearance with minimal dosing frequency, potentially just once or twice a year. Leveraging a unique portfolio of advanced antibodies engineered by Paragon Therapeutics, we target the fundamental mechanisms contributing to plaque psoriasis and other dermatologic and inflammatory conditions. Learn more about our vision at www.orukatx.com.

As we expand our core team, we are seeking passionate professionals who aspire to be part of a transformative journey, not just a job. If you are eager to make a positive impact and contribute to a vibrant, inclusive company culture, we want to hear from you.

Job Title: Associate Director, Downstream, Manufacturing Sciences and Technology (Biologics)

Location: Hybrid – Waltham, MA, with a requirement to be in-office 3 days a week.

Position Overview:

We are looking for a dynamic and skilled leader in Manufacturing Science and Technology (MSAT) to spearhead downstream late-stage and pivotal optimization, scale-up, and transfer of manufacturing processes. In this role, you will be responsible for process development, troubleshooting production challenges, data analysis, and ensuring adherence to regulatory standards to uphold product quality. The successful candidate will play a critical role in late-stage drug substance manufacturing and process validation activities to support BLA submissions. This position requires adaptability in a fast-paced environment, along with the ability to draft high-quality reports, finalize source documents, and actively participate in regulatory submissions. Join us as a vital member of a growing team dedicated to advancing best-in-class biotherapeutics.

About Oruka Therapeutics

Oruka Therapeutics is committed to setting a new benchmark in the treatment of chronic skin diseases through cutting-edge biologics. Our innovative approach is designed to provide lasting relief to patients and redefine standards of care in dermatology.

Similar jobs

Browse all companies, explore by city & role, or SEO search pages. View directory listings: all jobs, search results, location & role pages.

Tailoring 0 resumes

We'll move completed jobs to Ready to Apply automatically.