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Analytical Chemist I

NEPHRON SC, LLC
Posted a day ago, valid for a month
Location

West Columbia, SC, US

Salary

Competitive

Contract type

Full Time

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Sonic Summary

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  • The position involves supporting quality control testing and research and development activities through routine laboratory testing of various materials.
  • Candidates must possess a BS or MS in Chemistry, Biochemistry, or a related field, with 0-3 years of pharmaceutical experience preferred.
  • The role requires strong analytical skills, knowledge of cGMP regulations, and experience with analytical techniques such as FT-IR and UV/Vis spectroscopy.
  • The job entails data analysis, peer review, and compliance with laboratory guidelines while working under supervision.
  • Salary information is not explicitly stated, but the position is aimed at candidates with limited experience in the pharmaceutical industry.

Description

  

Job Purpose: The purpose of this position is to support quality control testing and research and development activities as needed by conducting routine laboratory testing for raw materials, in-process materials, finished product, and stability samples in accordance with approved analytical methods. 

   

Essential Duties and Responsibilities:

  • Conduct routine laboratory testing for raw materials, in-process materials and samples, finished product samples, and      stability samples in accordance with approved analytical methods. 
  • Conduct and execute laboratory work and testing using best-practice analytical techniques and follow laboratory GDP and cGMP requirements
  • Accurately analyze and interpret data using appropriate specifications and test methods. 
  • Accurately peer review notebooks and verify raw data to support sample release, including data generated in electronic      software systems.
  • Accurately enter data using appropriate reporting systems and release forms. 

Supplemental Functions: 

  •  Relies on instructions and pre-established guidelines to perform job functions.
  • Performs other similar duties as required.
  • Works under supervision.

Requirements

  

Knowledge & Skills: 

  • Strong analytical skills, problem-solving ability, and attention to detail.
  • An understanding of cGMP regulations pertaining to laboratory controls and knowledge of USP standards.
  • Ability to read, understand, review, and update Standard Operating Procedures, Forms, and Specifications and assist in      designing new procedures as necessary under management guidance.
  • Ability to perform testing for laboratory investigations for OOS and atypical QC test results under management guidance. 
  • Ability to effectively communicate within Chemistry Laboratory Staff and Management. 
  • Acknowledge and identify continuous improvement opportunities in all work activities. 
  • Ability to effectively use a multitude of resources to perform job functions accurately. 

Education/Experience: 

  • BS or MS in Chemistry, Biochemistry, or related field required with 0-3 years of pharmaceutical experience preferred.      Experience outside of pharmaceuticals in chemistry quality control or R&D will be considered for the highly qualified candidate.
  • Experience with conducting analysis by FT-IR, UV/Vis spectroscopy, and wet chemistry techniques is required. 
  • Experience in more advanced techniques such as HPLC and GC is preferred. 

    

Working Conditions / Physical Requirements:

  • This position requires bending, typing, lifting (up to 40 lbs.), standing, sitting and walking throughout the facility.
  • This position encounters the following environmental factors: hazardous materials including HPLC solvents, chemical reagents, acids, and other non-specified hazardous materials that are project specific.
  • This position requires safety glasses and other non-specified personal protective equipment to be worn as necessary. 



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