Exciting Chemist opening with a Pharma company near the Milwaukee, WI area.

SUMMARY:

The incumbent demonstrates proficiency through a wide exposure to pharmaceutical analyses and has a firm grasp of scientific principles and skill in applying this knowledge. The incumbent has practical experience in pharmaceutical analyses and routinely performs analysis in two of the functional areas (HPLC, GC, or Wet Chemistry).The incumbent performs and trains on routine chromatographic analyses. The incumbent works independently.

ESSENTIAL DUTIES AND RESPONSIBILITIES :

• Provides analytical support for production.
• Performs GC, HPLC and/or wet chemistry analyses on raw material, in process, stability and finished lot samples.
• Supports Analytical and Chemical Development by testing samples.
• Provides quick turnaround of in-process samples to production.
• Thoroughly documents all results in a laboratory notebook as well as compile all data into an ancillary.
• Empties HPLC and organic waste containers.
• Material sampling
• Performs daily equipment calibration on QC instrumentation
• Support laboratory investigation through testing.
• Performs all tasks in accordance with cGMP compliance.
• Assists in writing of SOPs, testing standards, protocols and reports.
• Assists in training of lab personnel on instrumentation, methods, and cGMP.
• Shares in the responsibilities of housekeeping (i.e. glassware, waste, retains, etc.)
• Provides ideas/feedback for areas where efficiency can improve.
• Has in-depth understanding of most analytical methods.
• Ability to troubleshoot most methods and equipment.
• Reviews and releases analytical results.
• Performs any other laboratory tasks deemed necessary by the manager.
• Adheres to personal moral, ethical, legal, and behavioral conduct that complies with the Code of Conduct.
• Adheres to all applicable SHE and cGMP regulations.

EDUCATION AND EXPERIENCE:

• A BA or BS in chemistry or related science and 1-5 years of work experience in a QC laboratory of a pharmaceutical batch plant is required.
• In-depth knowledge of cGMP is necessary.