Validation Scientist

Kelly Scientific Resources
November 14, 2020
Indianapolis, IN
Job Type


Validation Scientist - Indianapolis 
Direct Placement 
This is a professional mid-level technical position that will be responsible for the implementation and
maintenance of the QC analytical instruments and software systems, and writing, executing and
managing instrument qualification protocols.

  • Maintain QC analytical instruments and software systems.
  • Schedule PM and calibration of instruments with vendors. Maintain documentation of maintenance

performed for cGMP systems.

  • Initiate and manage Change Control requests for commissioning/decommissioning equipment and/or

software, new processes, and process improvements.

  • Initiate and oversee Capital Projects related to QC equipment, serving as Project Coordinator for

internal and external agencies.

  • Write, execute and summarize instrument IQ/OQ/PQ protocols.
  • Write/revise SOPs and ICMs for the use and maintenance of laboratory equipment and related

software, and conduct training as the Subject Matter Expert.

  • Perform periodic reviews of documents associated with equipment, to ensure they are kept up-to-date

and meet compliance requirements. Coordinates with analysts for timely investigation of out of specification
and non-conformance events related to instrumentation. Reviews investigation reports
for accuracy and completeness.

  • Perform weekly power cycling of all laboratory instrumentation.
  • Other duties as assigned.
  • As a part of the employee’s job requirements, the employee may be required to handle wastes

including hazardous wastes. The employee must attend mandatory annual hazardous waste training
meeting(s) and show a competency in that training by passing test

  • BS in chemistry or related discipline with a minimum of two years’ experience in the pharmaceutical


  • Demonstrated ability to perform analytical testing using the majority of the analytical equipment used

in the analytical laboratory including HPLC, GC, TLC, UV/VIS Spectroscopy, FTIR Spectroscopy,

  • Particle Size, Electrophoresis, etc.

  • Must have solid cGMP expertise in testing/manufacturing environments.
  • Technical knowledge of bio-analytical and chemistry analytical techniques: GC (Agilent), HPLC
  • (Waters, Wyatt), Chromatography Software (Waters Empower 3, Wyatt Astra), SDS-PAGE (GE, Bio-
  • Rad), TLC (Camag), UV/Vis Spectroscopy (Agilent, Thermo), FTIR Spectroscopy (Perkin Elmer),
  • Particle Size (Malvern), Osmometer (Wescor), Titration (Mettler Toledo, Metrohm)

Why Kelly®?

Kelly® Science & Clinical is your connection to premier scientific and clinical companies looking to hire talented people just like you. Every day, we match science professionals with dream jobs that fit their skills and interests—it’s the way we think job searching should be. Nearly 100 percent of our science recruiters have a professional background/education in science, so we know a thing or two about the science market and how to get you noticed.

About Kelly®

At Kelly, we’re always thinking about what’s next and advising job seekers on new ways of working to reach their full potential. In fact, we’re a leading advocate for temporary/non-traditional workstyles, because we believe they allow flexibility and tremendous growth opportunities that enable a better way to work and live. Connecting great people with great companies is what we do best, and our employment opportunities span a wide variety of workstyles, skill levels, and industries around the world.

Kelly is an equal opportunity employer committed to employing a diverse workforce and providing accommodations for people with disabilities in all parts of the hiring process as required under its Employment Accommodation Policy. Kelly will work with applicants to meet accommodation needs that are made known to Kelly in advance.

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