Job Description

Reference # : 17-07160Title : Research Associate
Location : South San Francisco, CA
Experience Level : Start Date / End Date : 09/04/2017 / 03/03/2019
Assignment Detail
Industry:Biotech/Pharma
Description

Research Associate

Be part of a company that delivers life-changing healthcare solutions. Eclaro is looking for a Research Associate for our client in South San Francisco, CA.
Eclaro’s client is among the world’s largest pharmaceutical companies, trusted by billions to provide superior, cutting-edge, and inexpensive medicine that improves health and well-being. If you’re up to the challenge, then take a chance at this rewarding opportunity!

Our Client is seeking a highly motivated, results-oriented, self-starter who demonstrates personal accountability for outcomes, to join a new and 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 contribute to the development, implementation and characterization of state-of-the-art processing technologies to deliver scalable and robust manufacturing processes, and support successful tech transfer for GMP manufacturing and release at a CMO. This position will also contribute to the development of Client technologies and approaches to meet future CART manufacturing needs and will work in close collaboration with key stakeholders including the CART Research and Bioprocess R&D groups.

RESPONSIBILITIES:
  • Actively contribute to development, implementation, characterization and successful execution of robust, state-of-the-art CART manufacturing processes.
  • Support clinical-scale non-GMP/ GMP IND-enabling manufacturing operations, including Tech Transfer to CMO and support of successful GMP manufacturing of clinical material.
  • Contribute to relevant and impactful innovation programs to enhance CART manufacturing technologies/ capabilities and work-processes (such as alternate transfection/ cell engineering strategies, media development, disposable/ closed production systems and automation), aligned with emerging business drivers and Regulatory expectations.
  • Contribute to Project Technical Teams and communicate and collaborate effectively to ensure effective interactions with all stakeholder groups
  • Demonstrate strong “personal leadership”/ accountability and technical and interpersonal skills, and apply scientific and technical experience to ensure safe, high-quality lab practices
  • Ensure high-quality, timely documentation in electronic laboratory notebooks and Technical Reports and contribute to Regulatory Filings and responses to Regulatory questions as appropriate.
  • Present data/ strategy to scientists (and management) in internal venues (technical meetings, Project Team meetings) as appropriate
  • Process development for manufacturing of cell or gene therapies
  • Culture and characterization of primary T cells, T cell molecular biology/ engineering
  • Molecular virology/ engineering and/ or production of recombinant viruses

EXPERIENCE/SKILLS REQUIRED:
  • Familiarity with cGMPs and relevant Regulatory Guidance documents a plus
  • Routine laboratory bench work involving prolonged standing and frequent walking
  • Occasional weekend and after-hour work is expected
  • Handling of biohazardous materials, including human blood samples (screened) and lentivirus is expected

If hired, you will enjoy the following Eclaro Benefits:
  • 401k Retirement Savings Plan administered by Merrill Lynch
  • TransitChek Pretax Commuter Benefits
  • Eligibility to purchase Medical, Dental & Vision Insurance through Eclaro

Interested in applying?
Contact Karyn Suayan at Karyn@eclaro.com now.



Equal Opportunity Employer: Eclaro values diversity and does not discriminate based on Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

Application Instructions

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