Analytical Chemist I

Company Info

Job Description

We are currently seeking an Analytical Chemist to join the Teva team on a contractual basis.

The Quality Control Laboratory Analytical Chemist 1, under the supervision of the QC Laboratory Manager/Analytical Chem V, is responsible for the preparation and reconciliation of test kits, testing reagents and volumetric solutions used in the analysis of QC samples associated with commercial production and stability samples. As an Analytical Chemist 1, responsibilities also extend to performing simple analytical testing and maintenance of inventory databases of analytical supplies.

Prepares analytical testing kits associated with commercial production and stability samples.

• Follows the QC Laboratory sample priority workload/plan generated by the Lab Operations Control Group to ensure the preparation of analytical testing kits in an efficient, safe and compliant (GMP) manner following all applicable Standard Operating Procedures and Analytical Testing Monographs.
• Retrieves and assembles in a timely manner laboratory materials and supplies required to carry out the testing specified in analytical monographs including reference standards, chromatographic columns, reagents, chemicals, volumetric solutions etc.
• Maintains the cleanliness and organization of all analytical supplies and materials in their designated locations in the QC Laboratory.
• Maintains the internal supply of testing reagents, chemicals and LIMS for tracking availability and location of laboratory materials, supplies, standards and HPLC/UPLC columns used in the QC Laboratory.
• Accounts for the return of all testing kits and contents once testing is completed and expedites retrieval of missing contents.
• Notifies other QC Laboratory service sections to ensure laboratory materials, chemicals and reference standards are ordered and available for subsequent test kit assembly.

Assists the supervisor with the execution and completion of analytical investigations carried out by QC Laboratory as required.

• • Performs the analytical investigation process ensuring that the following criteria and steps are adhered to as part of the process.
  
  

Performs all planning functions that are integral to the overall operation of the laboratory and in so doing, ensures that execution of work can be carried out in most cost effective and productive manner.

• • Executes the QC Laboratory workload/plan which includes but is not limited to raw materials, in-process, finish products, shelf life and accelerated stability programs, packaging components, process validation, analytical method transfer, technical services samples and microbiological testing

Qualifications

• College Diploma or University Degree in Chemistry or a related science.
• Knowledge of technical requirements as per compendia (USP/NF, BP/EP), in-house methods and general QC laboratory procedures.
• Knowledgeable in GMP/cGMP regulations as they apply to laboratories.
• Knowledge of analytical instrumentation (ex. HPLC, UPLC, GC, Dissolution), CDS (Chromatography Data System)
• LIMS (Laboratory Information Management System), CDS (Chromatography Data System), Trackwise, MSOffice, Oracle, SQC (SmartQC)

Function

Sub Function

Reports To

Senior Manager, Quality

Already Working @TEVA?

If you are a current Teva employee, please apply using the internal career site available on "Employee Central". By doing so, your application will be treated with priority. You will also be able to see opportunities that are open exclusively to Teva employees. Use the following link to search and apply: Internal Career Site

The internal career site is available from your home network as well. If you have trouble accessing your EC account, please contact your local HR/IT partner.

Teva’s Equal Employment Opportunity Commitment