Bench Scientist I

Job Description:

We are seeking a highly motivated, results-oriented, self-starter who demonstrates personal accountability for outcomes and thrives on increasing levels of responsibility, to join a dynamic team responsible for successful development and characterization of clinical-scale manufacturing processes for Chimeric Antigen Receptor T-cell (CART) therapies.

The successful candidate will help to develop and qualify analytical methods for the characterization, release and stability testing of CART products. An emphasis is on acquiring additional staff with experience in multipara metric immunophenotyping using flow cytometry.

• Actively contribute to successful development, qualification and execution of robust, state-of-the-art analytical methods for characterization of CART manufacturing processes and products

• Provide analytical support for clinical-scale non-GMP/ GMP IND-enabling manufacturing operations, including qualification of in-process and release methods and tech transfer internally and externally in support of GMP manufacturing and release of clinical material.

• Contribute to relevant and impactful innovation programs to enhance product characterization technologies.

• Contribute to project technical teams to ensure effective integration at all levels. Communicate and collaborate effectively.

• Demonstrate strong accountability as well as good organizational and interpersonal skills.

• Ensure high-quality, timely documentation in electronic laboratory notebooks and technical reports.

• Present data to scientists and management in internal venues (technical and project team meetings).

• Industry laboratory experience in a variety of analytical methods for the characterization and GMP release of cell-based or gene-therapies, especially cell-based and flow cytometry-related characterization/ release/ stability testing.

• Applied skills in molecular immunology/ T-cell biology and primary T cell culture/ expansion and characterization.

• Familiarity with cGMPs and relevant Regulatory Guidance documents.

• Laboratory work using qualified instrumentation, and technical analysis at provided work stations

Competency

• T-cell flow cytometry-

• Single-cell sequencing research

• T-cell biology

• Good laboratory practices (GLP)

• Responsible for general laboratory and operational support. Including providing logistical support for samples and compounds management, ordering supplies and carrying out general bench work activities.

Qualification:
BSc/ MSc degree in Immunology/ Molecular Biology with 3+ years of experience in biotech/ bio pharma industry (preferably in the development of analytical methods for the characterization of gene- or cell-based therapies).

Feel free to forward my email to your friends/colleagues who might be available. We do offer referral Bonus.

Thank you.

Kind Regards,

Harris Kaushik

Clinical Recruiter

Integrated Resources, Inc.

IT Life Sciences Allied Healthcare CRO

DIRECT # - (650)-399-0891

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