• Scientist II and III Biophysical Characterization AR&D

    Location US-NJ-Piscataway
    Posted Date 7 months ago(4/16/2018 12:35 PM)
    ID
    2018-2146
    Company
    Adello Biologics, LLC
  • Overview

    Adello Biologics is a privately held, U.S.-based biotechnology company that leads with science to accelerate development and drive manufacturing efficiency. The company's aim is to provide high-quality, affordable biosimilars to patients worldwide. Headquartered in Piscataway, NJ and driven by a team of highly skilled industry veterans, Adello is advancing a strategic pipeline of proteins and complex monoclonal antibodies with lead candidates in oncology and immunology. For more information, visit www.Adellobio.com

     

    Our vision is to make biosimilar medications affordable. We are seeking candidates interested in contributing to a bourgeoning field that has the potential to help millions of patients. As a growing company, Adello Biologics offers real development opportunities for candidates excited to take on responsibility, make an immediate impact and help us achieve our vision. As part of a close knit team, you’ll have the opportunity to work in a unique, high science industry while expanding your career. We are seeking a Scientist II Biophysical Characterization AR&D to be based out of our HQ in Piscataway, NJ.

    Responsibilities

    SUMMARY:

    We are seeking candidates interested in contributing to a bourgeoning field that has the potential to help millions of patients. As a growing company, Adello Biologics offers real development opportunities for candidates excited to take on responsibility, make an immediate impact and help us achieve our vision. As part of a close knit team, you’ll have the opportunity to work in a unique, high science industry while expanding your career. We are seeking a Scientist II-AR&D to be based out of our HQ in Piscataway, NJ.

     

    Essential Duties and Responsibilities:

    • Provide guidance to team members with respect to HPLC/UPLC troubleshooting, method development, method validation, etc.
    • Ensure adherence to highest quality and efficiency standards in laboratory operations (cGLP, cGMP)
    • Develop, optimize and validate new chromatography methods using literature references and scientific principles.
    • Implement and when necessary, optimize compendial test methods.
    • Independently write experiment summaries, development reports, technical reports, operation and test method procedure documents, and review documents comprising, but not limited to batch records, standard operating procedures, standard test methods, validation protocols and reports, etc.
    • Foster morale and teamwork

    Qualifications

    PREREQUISITES:

    Education:

    • Minimum B.S. degree in Analytical Chemistry, Biophysical/biochemical sciences, pharmaceutical sciences with 8-12 years industry experience
    • Or Master’s Degree in Biochemistry, Biotechnology, Biology with 6-10 years industry experience
    • Or Ph.D. in Biochemistry, Biotechnology, Biology with 2-5 years’ experience.

    Experience:

    • Experience with a wide variety of peptide mapping, HPLC and UPLC techniques including RPLC, SEC, HIC, IEX, at a minimum
    • Experience in the isolation and enrichment of product- and process-related impurities
    • Demonstrated leadership skills
    • Experience in method development, as well as method qualification/verification/validation in a GLP/GMP environment

     

    SPECIALIZED KNOWLEDGE AND SKILLS:

    • Excellent communication and technical writing skills
    • Ability to multitask technical responsibilities in a fast-paced, dynamic environment is required
    • Proficiency with the following software is required: Microsoft Word, Excel, PowerPoint, and Outlook.
    • Experience with Empower and/or ChemStation HPLC software programs is required.
    • Experience with any or all of the following is considered advantageous: spectroscopy (UV-Vis, CD, and fluorescence), mass spectrometry, DOE software, strong knowledge of statistics.

     

     WORK ENVIRONMENT AND PHYSICAL DEMANDS:

    General Work Environment:

    • Laboratory and controlled cleanroom space.
    • Cleanroom gowning required.

     

    Noise:

    • Standard noise levels expected with laboratory and manufacturing equipment.

     

    Standing/Lifting:

    • Extended periods of standing and walking while working in the manufacturing areas
    • Must be able to lift 15 lbs.

     

    Visual:

    • No special requirements

     

    Stress:

    • High paced demanding environment to meet manufacturing schedules

     

    Travel:

    • Travel not expected.

     

    Adello Biologics, LLC provides equal employment opportunities (EEO) to all employees and applicants for employment without regard to race, color, religion, sex, national origin, age, disability or genetics. In addition to federal law requirements, Adello Biologics, LLC complies with applicable state and local laws governing nondiscrimination in employment in every location in which the company has facilities. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, and transfer, leaves of absence, compensation and training.

     

    Notice To Agency And Search Firm Representatives  

    Adello Biologics is not accepting unsolicited resumes from agencies and/or search firms for this job posting. Resumes submitted to any Adello employee by a third party agency and/or search firm without a valid written & signed search agreement, will become the sole property of Adello. No fee will be paid if a candidate is hired for this position as a result of an unsolicited agency or search firm referral. Thank you.

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