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Senior Research Associate

TITLE:                Senior Research Associate
REPORTS TO:    Principal Scientist / Group Leader, Bioanalytical Services
LOCATION:       San Antonio Texas

 
The Company
Scorpion Biological Services is an innovation-driven contract research, development and biomanufacturing organization offering clients a customized, integrated, end-to-end solution for their large molecule discovery research, process and analytical method development, cGMP manufacturing, product characterization, release testing needs, and clinical trial support. Our approach enables us to forge collaborative client relationships that move beyond the traditional service outsourcing model into full product development collaborations.
 
Position Summary
ScorpionBio has an exciting opportunity for a Senior Research Associate to join the growing team of scientific staff in the Bioanalytical Services Group. This is a permanent, full-time role based in San Antonio, Texas.
 
Reporting directly to the Principal Scientist / Group Leader the candidate will work with the team to achieve the contract research and development milestones. The candidate will perform assay optimization, execution of assay qualification plans, and data analysis under the direction of Group Leader. The candidate will be involved in the execution of experimental protocols, and qualified assays in the GLP/ GMP setting. The employee will be involved in analytical work to support clinical trials as well as for CMC / biomanufacturing team. It is expected that up to 75% of the employee’s time will be spent at the bench.
 
The ideal candidate must be organized, motivated, and thrive in a fast-paced and dynamic biotech environment. She/he must be versatile and adapt to rapid change with a strong desire to make a significant impact.
Key Responsibilities:
●       Perform assays using conventional as well as spectral flow cytometers (capable of up to 40 parameter analysis). Perform data analysis using data analysis templates in FlowJo or FCS Express.
●       Perform multiplex ELISA using Luminex or MSD platforms.
●       Perform biochemical analysis using SPR/ Biacore, Maurice platforms.
●       Perform various tissue culture-based techniques (including magnetic cell separation/ enrichment, imaging) prior to flow cytometric or single cell proteomic analysis. 
●       Perform routine maintenance of flow cytometer, cell sorter, and other key instruments.
●       Execute method qualification plan, test method suitability plan, and test methods in GLP/GMP Quality System.
●       Records all data / procedures in the lab notebook / electronic lab notebook.
●       Execute laboratory workplans/schedules as per the client and / or company requirements.
●       Perform lot release testing, stability testing, and testing of clinical trial specimens.
●       Attend relevant training courses, meetings, and conferences.
Performs other work-related duties as assigned and directed by the Supervisor / Group Leader.
 
Education and Experience Requirements:

  • M.S or B.S. with 6+ years of relevant experience (Immunology/ virology/ cell biology / clinical research).
·      Experience of aseptic cell culture techniques is must. Experience in one or more area including flow cytometry, qPCR, SDS PAGE and Western Blotting, ELISA, multiplex ELISA is desirable.
  • Experience of working in Biotech/Biopharmaceutical industry/clinical research facility and following Good Laboratory Practices (GLP) and /or Good Manufacturing Practises (GMP) is plus.
 
Knowledge and Skills
●       Outstanding people skills, teamwork, ability to build strong relationships with cross-functional team members and lead by example.
●       Ability to take responsibility and “get the job done” in a high-energy, high-intensity, results-oriented environment.
●       Excellent verbal and written communication skills, strong presentation skills.
●       Must possess good to excellent writing and PC skills with a knowledge base in Microsoft Word, Excel, Power Point, and Project.
●       Working knowledge of FDA and other regulatory agency guidelines is preferred.
 
Working Hours
 
·      Full Time, 40 hours per week
·      Flexibility is required, some weekend work may be needed and earlier or later start, and finish times may also be required.