Quality Control Analyst I Albany Molecular Research Rensselaer

Title Quality Control Analyst I
Date 16 May 2020
Company Albany Molecular Research
City Rensselaer

Short Description :

Related discipline OR equivalent combination of relevant education and experience may be substituted as appropriate Maintain compliance with all regulations at the federal, state, and local levels, as well as appropriate SOPs Develop and maintain working knowledge ,…

Full Description :

QC Analyst I in Rensselaer, NY Inc. provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries.
The principal responsibility of the QC Analyst I is the analysis of chemical intermediates and target compounds. The QC Analyst I is expected to demonstrate expertise in both the theoretical and practical aspects of analytical chemistry. A major component in the scientist’s performance rating will be based on productivity.
  • Conduct laboratory operations in a safe manner. Maintain familiarity with the Chemical Hygiene Plan. Exhibit safety awareness and safe work practices.
  • Follow responsible actions regarding chemical disposal. Maintain compliance with all regulations at the federal, state, and local levels, as well as appropriate SOP’s.
  • Develop and maintain working knowledge of commonly used spectroscopic and chromatographic procedures. Establish a demonstrated expertise in at least one technique.
  • Write analytical method procedures to establish format.
  • Write analytical validation reports.
  • Use sound judgment and previously acquired knowledge and experience to develop new procedures for new compounds.
  • Process samples with the standard procedures effectively and independently. Analyze experimental data for validity before reporting results.
  • Use and maintain equipment in a neat and orderly manner. Report any malfunction immediately to supervisor. Repair minor problems. Maintain service and calibration records.
  • Keep contemporary, accurate, legible, and complete experimental records in accordance with GMP and GLP practices.
  • Use technical and regulatory knowledge and judgment to validate procedures to comply with internal SOPs and regulatory needs with minimal supervision.
  • Submit complete, documented, and legible reports of analytical testing. Ensure that data is properly filed and accessible for review in accordance with appropriate SOP’s.
  • Recommend and implement methods to increase the quality of products and/or services.
  • Establish new and improved ways to perform job by challenging established procedures.
  • Discuss routinely with supervisor the status of assigned programs and potential problems.
  • Organize work time so that multiple activities run concurrently. Use time efficiently to accomplish immediate task and perform other needed activities.
  • Manage workload and time to enable the incumbent to perform multiple projects effectively, and ensure all necessary paperwork is completed on a timely basis.
  • Volunteer to assist with other tasks in the analytical function not directly related to specific projects.
  • Participate in self-development activities. Provide orientation and train new personnel on operating procedures and policies.
  • Perform other related duties as may be reasonably assigned in the course of business.

Qualifications Required:
  • Bachelor’s with major in a Natural Science or related discipline OR equivalent combination of relevant education and experience may be substituted as appropriate

Preferred:
  • Chromatography experience
  • Chemical Hygiene training
  • Other pertinent training/courses

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