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QC Method Analyst

QC Method Analyst

Cytovance Biologics IncOklahoma City, OK, US
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Job Description

Job Description

General Summary :

The QC Method Analyst will participate in the assay performance, qualification / validation of assays and laboratory equipment, and transfer of standard protein characterization methods. Duties will be carried out in accordance with quality standards and procedures set by the company and applicable government agencies.

Essential Duties and Responsibilities :

  • Participate in qualification / validation of analytical methods.
  • Assist in preparation of method qualification / validation protocols, reports, and test method SOPs.
  • Author / execute method transfer protocols for various analytical methods for the characterization of biopharmaceutical protein products.
  • Work on developing and improving assays for various projects as needed.
  • Work under general supervision of QC Scientist / Senior Scientist to meet project goals in a timely manner.
  • Specify and source new analytical equipment as required to expand the testing capabilities of the QC Analytical Laboratory.
  • Assist with the overall maintenance and calibration of the QC laboratory analytical equipment as needed.
  • Analyze laboratory data for trending.
  • Support the training of new and existing laboratory personnel.
  • Evaluates technology transfers associated with new products or processes.
  • Other duties as assigned.

Job Requirements :

  • B.S. in Life Sciences / Chemistry.
  • 3-4 years of industry experience is expected. Higher educational qualification and relevant laboratory experience will also be considered for this position.
  • Working experience with a range of protein analytical / biomolecular / bioanalytical techniques including HPLC, UPLC, ELISA, Spectrophotometric analysis of proteins, enzymatic activity assay, and electrophoretic analysis of proteins (SDS-PAGE, Western blots, IEF and CE) procedures.
  • Working knowledge of ICH, ISO and GMP regulatory compliance requirements related to product testing and stability testing will be preferred.
  • Should have demonstrated leadership qualities within a team working environment.
  • Ability to work on a project independently.
  • Experience in a GMP Laboratory / environment is plus.
  • Organizational, multitasking, problem-solving, math, statistical, interpersonal, written, and oral communication skills. Detail-oriented and ability to prioritize work.
  • Must be able to work within multifunctional teams.
  • Ability to function well in a fast-paced multiple project environment.
  • Communicates openly with development, production & quality personnel to resolve problems before or as they arise.
  • Physical Demands :

    While performing the duties of this job, the employee is frequently required to stand; sit and talk or hear. The employee is occasionally required to walk; use hands to finger, handle, or feel; reach with hands and arms; climb or balance and stoop, kneel, crouch, or crawl.

    Work Environment :

    While performing the duties of this Job, the employee is occasionally exposed to fumes or airborne particles and toxic or caustic chemicals. The noise level in the work environment is usually moderate.

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    QC Method Analyst • Oklahoma City, OK, US