Research Coordinator II

Job Purpose

The primary role for the candidate will be assisting in contract manufacturing management in a cleanroom GMP facility at the Center for Cell and Gene Therapy. The position would require training on GMP procedures.

Job Duties
  • Review and compile batch records. Make sure all the worksheets are turned in for review, results tuned in, such as sterility results, etc.
  • Provide documents to external client. Scan completed batch records, validation reports, de-identify information, if necessary.
  • Draft Standard Operating Procedures, validation plans and performing appropriate validations.
  • Assist with supply maintenance/ordering for third party protocol (e.g. keep track if critical supplies are available, for example Sepax kits and buffers, printer labels and ribbons, everything that is Tessa specific.
  • Assist with general external client requests, such as shipping and collecting the data.

Minimum Qualifications
  • Bachelor's degree in a related field. Four years of related experience may substitute for degree requirement.
  • One year of relevant experience is required.

  • Participate in conference calls with clients from oversea, therefore flexibility of work before 8 am and after 5 pm regular schedule will be occasionally required.
  • Regular interaction within internal laboratories in CAGT GMP and with external clients.

Baylor College of Medicine is an Equal Opportunity/Affirmative Action/Equal Access Employer.



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