317BR, Senior Scientist / Scientist, CMC Bioinformatics

Job Code 317BR

Description

Fate Therapeutics is seeking a self-motivated and enthusiastic individual with expertise in bioinformatics and data management to join the Process and Assay Development team. The successful candidate will be responsible for developing automated data analysis workflows and creating data analytics solutions to support the development of engineered iPSC-derived NK and T cell manufacturing processes. The individual will work closely with Process and Assay Development scientists to establish, implement, and maintain automated flow cytometry data analysis workflows to characterize Fate’s products. The individual will also partner with the Manufacturing and QC and MSAT teams to develop data QC, integration, and analysis strategies to characterize Fate’s manufacturing platform and products. This is a full-time position reporting to the Director, Process and Assay Development and is located at our corporate headquarters in San Diego.

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For consideration send cover letter and curriculum vitae to: careers@fatetherapeutics.com and reference job 317BR.

About Fate Therapeutics, Inc.

Fate Therapeutics is a biopharmaceutical company dedicated to the development of programmed cellular immunotherapeutics for the treatment of cancer and immune disorders. The Company’s cell-based product candidate pipeline is comprised of off-the-shelf immuno-oncology therapeutics, including NK- and T-cell-based candidates derived from induced pluripotent cells, and immuno-regulatory therapeutics, including hematopoietic cell-based candidates for protecting the immune system of patients undergoing hematopoietic cell transplantation and for suppressing auto-reactive T cells of patients with auto-immune disorders. Its adoptive cell therapy candidates are based on the Company’s novel ex vivo cell programming approach, which it applies to modulate the therapeutic function and direct the fate of immune cells.

316TL, Scientist / Associate Scientist, Protein Chemistry / Molecular Engineering

Job Code 316TL

Description

Fate Therapeutics is currently seeking a talented and motivated individual with expertise in protein chemistry and molecular biology to join a multidisciplinary team dedicated to discovery and productization of novel off-the-shelf cell-based immunotherapies. Initially the candidate will perform production and functional assessment of research-grade recombinant proteins to support Fate’s gene editing platform and preclinical pipelines. The position will evolve to include establishment of qualified protocols for expression, purification, and analytical assays for protein batches used in the manufacturing process of genetically engineered induced pluripotent stem cells (iPSCs). Candidate is highly desired to master the entire process of recombinant protein production and to independently design and deliver high quality results to meet Fate’s aggressive timelines. This is a full-time position that reports to the Director, Molecular Engineering and is located at the company’s corporate headquarters in San Diego.

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For consideration send cover letter and curriculum vitae to: careers@fatetherapeutics.com and reference job 316TL.

About Fate Therapeutics, Inc.

Fate Therapeutics is a biopharmaceutical company dedicated to the development of programmed cellular immunotherapeutics for the treatment of cancer and immune disorders. The Company’s cell-based product candidate pipeline is comprised of off-the-shelf immuno-oncology therapeutics, including NK- and T-cell-based candidates derived from induced pluripotent cells, and immuno-regulatory therapeutics, including hematopoietic cell-based candidates for protecting the immune system of patients undergoing hematopoietic cell transplantation and for suppressing auto-reactive T cells of patients with auto-immune disorders. Its adoptive cell therapy candidates are based on the Company’s novel ex vivo cell programming approach, which it applies to modulate the therapeutic function and direct the fate of immune cells.

315AM, Manager, Clinical Drug Supply

Job Code 315AM

Description

Fate is currently seeking a motivated Supply Manager to join our Technical Operations team. The successful candidate will be responsible for Investigational Product (IP) supply operations for multiple clinical trials and for managing the IP distribution process. The successful candidate will have excellent organizational and communication skills, a keen attention to detail and thrive in a team environment. This is a full-time position reporting to the Sr. Director of Manufacturing and QC and is located at our corporate headquarters in San Diego, California.

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For consideration send cover letter and curriculum vitae to: careers@fatetherapeutics.com and reference job 315AM.

About Fate Therapeutics, Inc.

Fate Therapeutics is a biopharmaceutical company dedicated to the development of programmed cellular immunotherapeutics for the treatment of cancer and immune disorders. The Company’s cell-based product candidate pipeline is comprised of off-the-shelf immuno-oncology therapeutics, including NK- and T-cell-based candidates derived from induced pluripotent cells, and immuno-regulatory therapeutics, including hematopoietic cell-based candidates for protecting the immune system of patients undergoing hematopoietic cell transplantation and for suppressing auto-reactive T cells of patients with auto-immune disorders. Its adoptive cell therapy candidates are based on the Company’s novel ex vivo cell programming approach, which it applies to modulate the therapeutic function and direct the fate of immune cells.

314BR, Associate Director / Senior Manager, Analytical Development

Job Code 314BR

Description

Fate Therapeutics is seeking a highly-motivated individual with a breadth of analytical development expertise to provide scientific and technical leadership to the analytical and assay development team. The successful candidate will be responsible for establishing analytical strategies and techniques in support of process and product development of engineered iPSC-derived NK and T cell therapies and the development and implementation of best-in-class analytical testing strategies to control and characterize Fate’s products. Operating in a cross-functional and dynamic environment, the individual will partner with Process Development, Quality Control, Manufacturing Sciences and Technology, Product Development, Regulatory Affairs, and Manufacturing teams. The ideal candidates should have experience managing daily operations of a team, a proven track record of providing leadership to accelerate clinical product development, and implementing analytical testing methods that are compliant with regulatory requirements. This is a full-time position reporting to the Director, Process and Assay Development and is located at our corporate headquarters in San Diego.

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For consideration send cover letter and curriculum vitae to: careers@fatetherapeutics.com and reference job 314BR.

About Fate Therapeutics, Inc.

Fate Therapeutics is a biopharmaceutical company dedicated to the development of programmed cellular immunotherapeutics for the treatment of cancer and immune disorders. The Company’s cell-based product candidate pipeline is comprised of off-the-shelf immuno-oncology therapeutics, including NK- and T-cell-based candidates derived from induced pluripotent cells, and immuno-regulatory therapeutics, including hematopoietic cell-based candidates for protecting the immune system of patients undergoing hematopoietic cell transplantation and for suppressing auto-reactive T cells of patients with auto-immune disorders. Its adoptive cell therapy candidates are based on the Company’s novel ex vivo cell programming approach, which it applies to modulate the therapeutic function and direct the fate of immune cells.

313LS, Senior Manufacturing Associate / Manufacturing Associate

Job Code 313LS

Description

Fate Therapeutics is seeking an experienced and highly motivated manufacturing technician to join our manufacturing team to support operation of the cGMP clean room suite in a variety of production activities related to Fate’s cell therapy clinical trials. The successful candidate will develop and adhere to written procedures (SOPs) related to housekeeping, monitoring of equipment and facilities, and manufacturing of cell therapies internally at Fate. This person demonstrates cGMP compliance and support for manufacturing activities across multiple programs. This is a full-time position initially reporting to the Associate Director, Manufacturing, and is located at our corporate headquarters in San Diego, CA.

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For consideration send cover letter and curriculum vitae to: careers@fatetherapeutics.com and reference job 313LS.

About Fate Therapeutics, Inc.

Fate Therapeutics is a biopharmaceutical company dedicated to the development of programmed cellular immunotherapeutics for the treatment of cancer and immune disorders. The Company’s cell-based product candidate pipeline is comprised of off-the-shelf immuno-oncology therapeutics, including NK- and T-cell-based candidates derived from induced pluripotent cells, and immuno-regulatory therapeutics, including hematopoietic cell-based candidates for protecting the immune system of patients undergoing hematopoietic cell transplantation and for suppressing auto-reactive T cells of patients with auto-immune disorders. Its adoptive cell therapy candidates are based on the Company’s novel ex vivo cell programming approach, which it applies to modulate the therapeutic function and direct the fate of immune cells.

312MW, Quality Assurance Associate, Product Manufacturing / cGMP

Job Code 312MW

Description

Fate’s Quality Assurance (QA) group is seeking a motivated and talented individual to support operational QA for drug substance/drug product manufacturing. The successful candidate will assure adherence to standard operating procedures, GXP guidelines, and applicable regulations. The ideal candidate will have experience working in a cGMP environment and have hands-on experience in operational QA a.k.a person-in-plant (PIP). Candidates must thrive in a fast-paced team environment and must have excellent attention to detail, communication, organizational abilities, and independent problem-solving skills. This is a full-time position reporting to the Senior Manager, Quality Assurance, and is located at our company’s headquarters in San Diego, California.

Download a PDF of the job description for more details:

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For consideration send cover letter and curriculum vitae to: careers@fatetherapeutics.com and reference job 312MW.

About Fate Therapeutics, Inc.

Fate Therapeutics is a biopharmaceutical company dedicated to the development of programmed cellular immunotherapeutics for the treatment of cancer and immune disorders. The Company’s cell-based product candidate pipeline is comprised of off-the-shelf immuno-oncology therapeutics, including NK- and T-cell-based candidates derived from induced pluripotent cells, and immuno-regulatory therapeutics, including hematopoietic cell-based candidates for protecting the immune system of patients undergoing hematopoietic cell transplantation and for suppressing auto-reactive T cells of patients with auto-immune disorders. Its adoptive cell therapy candidates are based on the Company’s novel ex vivo cell programming approach, which it applies to modulate the therapeutic function and direct the fate of immune cells.

311MW, Document Control Associate, Quality Assurance

Job Code 311MW

Description

Fate’s Quality Assurance (QA) group is seeking a motivated and talented individual to support development and implementation of the Document Control program. The successful candidate will assure adherence to standard operating procedures, GXP guidelines, and applicable regulations. The ideal candidate will have experience working in a cGMP environment, and have hands-on experience in document management, change control, and training. Candidates must thrive in a fast-paced team environment and must have excellent attention to detail, communication, organizational abilities, and independent problem-solving skills. This is a full-time position reporting to the Senior Manager, Quality Assurance, and is located at our company’s headquarters in San Diego, California.

Download a PDF of the job description for more details:

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For consideration send cover letter and curriculum vitae to: careers@fatetherapeutics.com and reference job 311MW.

About Fate Therapeutics, Inc.

Fate Therapeutics is a biopharmaceutical company dedicated to the development of programmed cellular immunotherapeutics for the treatment of cancer and immune disorders. The Company’s cell-based product candidate pipeline is comprised of off-the-shelf immuno-oncology therapeutics, including NK- and T-cell-based candidates derived from induced pluripotent cells, and immuno-regulatory therapeutics, including hematopoietic cell-based candidates for protecting the immune system of patients undergoing hematopoietic cell transplantation and for suppressing auto-reactive T cells of patients with auto-immune disorders. Its adoptive cell therapy candidates are based on the Company’s novel ex vivo cell programming approach, which it applies to modulate the therapeutic function and direct the fate of immune cells.

310MW, Manager, Quality Assurance

Job Code 310MW

Description

Fate Therapeutics is seeking an experienced and motivated Manager of Quality Assurance to support Fate’s internal and external cGMP manufacturing operations. The successful candidate must thrive in a fast-paced team environment, have excellent communication, planning and organizational skills, and manage quality assurance activities to meet Fate’s priorities and timelines. The candidate must have experience and a proven track record of establishing and maintaining a quality management system to support GXP-compliant manufacturing operations and will be expected to effectively follow Fate’s SOPs and policies. This is a full-time position reporting to the Quality Assurance Senior Manager and is located at our corporate headquarters in San Diego, California.

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For consideration send cover letter and curriculum vitae to: careers@fatetherapeutics.com and reference job 310MW.

About Fate Therapeutics, Inc.

Fate Therapeutics is a biopharmaceutical company dedicated to the development of programmed cellular immunotherapeutics for the treatment of cancer and immune disorders. The Company’s cell-based product candidate pipeline is comprised of off-the-shelf immuno-oncology therapeutics, including NK- and T-cell-based candidates derived from induced pluripotent cells, and immuno-regulatory therapeutics, including hematopoietic cell-based candidates for protecting the immune system of patients undergoing hematopoietic cell transplantation and for suppressing auto-reactive T cells of patients with auto-immune disorders. Its adoptive cell therapy candidates are based on the Company’s novel ex vivo cell programming approach, which it applies to modulate the therapeutic function and direct the fate of immune cells.

309MD, Clinical Trial Manager

Job Code 309MD

Description

Fate’s Clinical Operations team is currently seeking a talented and motivated clinical operations professional to support our clinical trials. The successful candidate must have experience managing Phase I-III trials and a good knowledge of clinical operations, GCP and FDA regulatory environment. Oncology trial experience preferred. This is a full-time position reporting to the Associate Director, Clinical Operations, and is located at our Company’s headquarters in San Diego, California.

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For consideration send cover letter and curriculum vitae to: careers@fatetherapeutics.com and reference job 309MD.

About Fate Therapeutics, Inc.

Fate Therapeutics is a biopharmaceutical company dedicated to the development of programmed cellular immunotherapeutics for the treatment of cancer and immune disorders. The Company’s cell-based product candidate pipeline is comprised of off-the-shelf immuno-oncology therapeutics, including NK- and T-cell-based candidates derived from induced pluripotent cells, and immuno-regulatory therapeutics, including hematopoietic cell-based candidates for protecting the immune system of patients undergoing hematopoietic cell transplantation and for suppressing auto-reactive T cells of patients with auto-immune disorders. Its adoptive cell therapy candidates are based on the Company’s novel ex vivo cell programming approach, which it applies to modulate the therapeutic function and direct the fate of immune cells.

307GH, Senior Facilities Technician, Calibration and Equipment Management

Job Code 307GH

Description

Fate Therapeutics is seeking a talented and highly motivated individual to work with our Manufacturing, Process Sciences, and R&D teams to provide hands-on Calibration and Metrology support. The successful candidate will schedule and perform maintenance of equipment utilized by end-users, in conjunction with third party resources. The successful candidate will support the Facilities Department complying with cGMP SOPs and applying GDP (Good Documentation Practices). This individual will oversee that contractors are trained on our SOPs and complete the tasks in a compliant manner, ensuring that the necessary documentation is completed accurately. This is a full-time position reporting to the Director, Facilities and is located at our corporate headquarters in San Diego, California.

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For consideration send cover letter and curriculum vitae to: careers@fatetherapeutics.com and reference job 307GH.

About Fate Therapeutics, Inc.

Fate Therapeutics is a biopharmaceutical company dedicated to the development of programmed cellular immunotherapeutics for the treatment of cancer and immune disorders. The Company’s cell-based product candidate pipeline is comprised of off-the-shelf immuno-oncology therapeutics, including NK- and T-cell-based candidates derived from induced pluripotent cells, and immuno-regulatory therapeutics, including hematopoietic cell-based candidates for protecting the immune system of patients undergoing hematopoietic cell transplantation and for suppressing auto-reactive T cells of patients with auto-immune disorders. Its adoptive cell therapy candidates are based on the Company’s novel ex vivo cell programming approach, which it applies to modulate the therapeutic function and direct the fate of immune cells.