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Manufacturing Sciences and Technology (MSAT) Process Engineer (3rd Shift)

Improve the efficiency and safety of drug product manufacturing processes at a late-stage biotechnology company.

Location
Princeton, NJ
Compensation
Not disclosed
Level
mid
Type
full time · On-site

Posted by employer 1 month ago

First seen on Joblaze 1 week ago

Last verified on the company career page 1 day ago

Apply at Orca Bio → Save job Scanned from orcabio.com

Not disclosed in this posting: compensation, years of experience, visa sponsorship.

Joblaze summary

The MSAT Process Engineer at Orca Bio focuses on enhancing the efficiency and safety of the manufacturing processes for cell therapies. This role requires expertise in process monitoring, troubleshooting, and implementing improvements, alongside a strong background in life cycle management of clinical and commercial products. Ideal candidates are likely to have experience in biotechnology or pharmaceutical manufacturing, particularly at a mid to senior level. Orca Bio is in a critical phase of establishing its East Coast operations, aiming to support the delivery of innovative therapies.

Joblaze insights

Quick facts

Is the Manufacturing Sciences and Technology (MSAT) Process Engineer (3rd Shift) role remote?
No — this is an on-site role in Princeton, NJ.
Where is the role based?
Orca Bio is hiring for this position in Princeton, NJ.
What seniority level is this role?
Orca Bio targets mid-level candidates for this position.
Is this full-time or contract?
Full-time for this Manufacturing Sciences and Technology (MSAT) Process Engineer (3rd Shift) role at Orca Bio.

From the original posting

More than one million people in the United States today are fighting blood cancer. While a traditional allogeneic stem cell transplant has been the best hope for many, the transplant itself can prove fatal or lead to serious conditions, such as graft vs. host disease. Orca Bio is a late-stage biotechnology company redefining the transplant process by developing next-generation cell therapies with the goal of providing significantly better survival rates with dramatically fewer risks. With our purified, high-precision investigational cell therapies we hope to not only replace patients' blood and immune systems with healthy ones, but also restore their lives.   We are establishing manufacturing operations on the East Coast to ensure the consistent and reliable delivery of our high-precision cell therapy products. This site is essential to advancing our clinical pipeline and supporting future commercial availability of our life-saving therapies.   The MSAT Process Engineer works to improve the efficiency and safety of the drug product manufacturing process.  This role is responsible for life cycle management of clinical and commercial products including process monitoring and troubleshooting, implementation and validation of process improvements and changes, and supporting investigations and corrective/preventive actions.