REQUIREMENTS:

• Bachelor’s degree in a physical science, preferred.
• A minimum of three years in a quality control analytical lab required without a bachelor’s degree.
• Preferred experience with analytical chemistry, instrumental analysis, data compilation, and USP/NF procedures and knowledge of cGMPs.
• Must have good organizational skills, decision-making skills, and communication skills.
• Strong technical writing skills.
  Location:
  3702 E. 21st St.
  Indianapolis, Indiana, 46218
  United States
  Colorcon participates in E-Verify and will provide the federal government with your Form I-9 information to confirm that you are authorized to work in the U.S. If E-Verify cannot confirm that you are authorized to work, this employer is required to give you written instructions and an opportunity to contact Department of Homeland Security (DHS) or Social Security Administration (SSA) so you can begin to resolve the issue before the employer can take any action against you, including terminating your employment. Employers can only use E-Verify once you have accepted a job offer and completed the Form I-9.
  E-Verify Works for Everyone
  For more information on E-Verify, or if you believe that your employer has violated its E-Verify responsibilities, please contact DHS.

RESPONSIBILITIES & DUTIES:

• Analyzes raw materials, intermediates and products by physical, chemical and instrumental techniques in accordance with established procedures with some supervision.
• Ensures the laboratory is in working order, which includes but is not limited to keeping inventory of chemicals and consumables needed in the lab and calibrating equipment when needed.
• Submits accurate, precise and complete analytical reports in a timely fashion; Communicates OOS results.
• Reviews the work of colleagues and other departments as needed.
• Exhibits a working knowledge of Colorcon’s Oracle database applications to maintain accuracy of records.
• Aware of cGMPs and cGLPs and maintains compliance with those regulations; Documents all activities associated with cGMP compliance (i.e. instrument calibration, OOS investigations etc.)
• Demonstrates the ability to set priorities, with some supervision, based on Operation’s schedules and deadlines.
• Interdepartmental communication with operations (Operators and Shift Leaders) concerning the use of materials evaluated.
• Performs special analyses and special project testing on a request basis as needed.
• Assists with OOS investigations as needed.
• Maintains good housekeeping, order, and safety in the laboratory.