3 Engineer III, Cell Therapy Process Engineering Jobs in Boston, MA
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Engineer III, Cell Therapy Process Engineering
$110k-134k (estimate)
Full Time | Contract Research
2 Days Ago
CRISPR Therapeutics is Hiring an Engineer III, Cell Therapy Process Engineering Near Boston, MA
Company OverviewSince its inception over a decade ago, CRISPR Therapeutics has transformed from a research-stage company advancing programs in the field of gene editing, to a company with a diverse portfolio of product candidates across a broad range of disease areas including hemoglobinopathies, oncology, regenerative medicine, cardiovascular and rare diseases. The Nobel Prize-winning CRISPR science has revolutionized biomedical research and represents a powerful, clinically validated approach with the potential to create a new class of potentially transformative medicines. To accelerate and expand its efforts, CRISPR Therapeutics has established strategic partnerships with leading companies including Bayer and Vertex Pharmaceuticals. CRISPR Therapeutics AG is headquartered in Zug, Switzerland, with its wholly-owned U.S. subsidiary, CRISPR Therapeutics, Inc., and R&D operations based in Boston, Massachusetts and San Francisco, California, and business offices in London, United Kingdom.
Position SummaryAs part of the Stem Cell Engineering Group, we are seeking an Engineer III to join an exciting team that is broadening the application of stem cells through gene editing. The successful candidate will be integral in developing stem cell-derived therapies for regenerative medicine. This role will be responsible for preparing early-stage cell therapy processes for clinical manufacturing by participating in process development and supporting technology transfer to manufacturing sites. A successful candidate will have strong process development skills and a robust understanding of cell therapy manufacturing processes. The position requires enthusiasm, passion, self-motivation, attention to detail, and a desire to create novel therapies for patients.
Responsibilities
CRISPR Therapeutics, Inc. is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law.
To view our Privacy Statement, please click the following link: http://www.crisprtx.com/about-us/privacy-policy
Position SummaryAs part of the Stem Cell Engineering Group, we are seeking an Engineer III to join an exciting team that is broadening the application of stem cells through gene editing. The successful candidate will be integral in developing stem cell-derived therapies for regenerative medicine. This role will be responsible for preparing early-stage cell therapy processes for clinical manufacturing by participating in process development and supporting technology transfer to manufacturing sites. A successful candidate will have strong process development skills and a robust understanding of cell therapy manufacturing processes. The position requires enthusiasm, passion, self-motivation, attention to detail, and a desire to create novel therapies for patients.
Responsibilities
- Develop robust, scaled platform for pluripotent stem cell expansion and directed differentiation.
- Develop protocols and technologies in support of all stages of product development, including upstream and downstream processing, from clinical to commercial scale.
- Design and execute experiments that support decision making.
- Facilitate technology transfer and clinical manufacturing through document preparation, technical support, and effective communication.
- B.S./B.E./M.S. in Life Sciences, bioengineering, chemical engineering, or related discipline with 4 to 7 years of relevant research experience or 2-5 years with advanced degree.
- Demonstrated experience with aseptic cell culture methods, including cryopreserving, thawing, and expanding cell lines.
- Process development experience in a bio-pharmaceutical setting working with interdisciplinary and cross-functional teams.
- Experience working with bioreactors.
- Ability to communicate effectively with a diverse range of scientists and engineers.
- Track record of intellectually challenging oneself to enhance scientific abilities.
- Ability to work independently as well as part of a results-oriented research team.
- Highly organized with significant attention to detail.
- Experience in maintenance and differentiation of human pluripotent stem cells.
- Prior experience in downstream processing, especially with cell processing systems.
- Experience with technology transfer.
- Experience supporting clinical manufacturing and/or regulatory filings.
- Collaborative – Openness, One Team
- Undaunted – Fearless, Can-do attitude
- Results Orientation – Delivering progress toward our mission. Sense of urgency in solving problems.
- Entrepreneurial Spirit – Proactive. Ownership mindset.
CRISPR Therapeutics, Inc. is committed to equal employment opportunity and non-discrimination for all employees and qualified applicants without regard to a person's race, color, gender, age, religion, national origin, ancestry, disability, veteran status, genetic information, sexual orientation or any characteristic protected under applicable law.
To view our Privacy Statement, please click the following link: http://www.crisprtx.com/about-us/privacy-policy
Job Summary
JOB TYPE
Full Time
INDUSTRY
Contract Research
SALARY
$110k-134k (estimate)
POST DATE
06/27/2024
EXPIRATION DATE
08/23/2024
WEBSITE
crisprtx.com
HEADQUARTERS
Cambridge, MA
SIZE
200 - 500
INDUSTRY
Contract Research
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