Performs chemical analysis on purchased raw materials, in-process preparations, pure drug substances and finished pharmaceutical products to determine that they meet official compendial and/or Pfizer requirements.
+ Perform standard qualitative and quantitative analysis on purchased raw materials, in-process products, pure drug substances, finished pharmaceutical preparations, stability samples, and contract manufacturing samples utilizing accepted gravimetric and spectrophotometric procedures, in accordance with approved testing procedures Pfizer, the National Formulary (NF), and the United States Pharmacopeia (USP).
+ Utilizes standard analytical chemistry techniques.
+ Prepare and standardize volumetric solutions, test solutions and reagents used in USP, NF and Pfizer monograph analysis.
+ Maintain records of all analysis information of assigned products for permanent file and proper entry of information on laboratory forms.
+ Evaluate all data obtained from analysis; if discrepancy or deviation occurs, consult with supervisor.
+ Review completed data for accuracy before forwarding data to QA filing in the batch record.
+ Participate in employee involvement team(s).
+ Any other duties as assigned by supervisor.
Bachelor’s Degree in Chemistry, Biochemistry or related science
0-1 years of experience in a laboratory setting
Considerable mental/visual concentration, coordinating manual dexterity with mental/visual attention – including alternating sitting/standing to perform tasks and strict documentation requirements.
**Other Job Details:**
+ **Last Date to Apply for Job: May 9, 2020** Eligible for Relocation PackageEligible for Employee Referral Bonus
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**EEO & Employment Eligibility**
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