Quality Control Analyst II (2nd Shift)

About this opportunity :

The QC Analyst II is responsible for conducting routine and non-routine analyses of raw materials, in-process materials and finished products in accordance with cGMP guidelines. The appropriately trained individual may provide training and guidance to other QC Analysts. The individual troubleshoots problems associated with methods and instruments resolving them where possible or seeking guidance/authorization where required. This is a second shift role.

Key Responsibilities:

• Conduct a wide variety of routine testing.
• Test and analyze samples in a timely manner in support of project plans in accordance with cGMP guidelines.
• Review data for compliance against specifications and GMP regulations.
• Generate stability reports, and assist in the development of experimental procedures and protocols
• Assist with developing/revising documentation such as SOP, testing procedures and material specifications.
• Provide training and guidance to other analysts.

Required Skills/Abilities:

• BS in chemistry, biology, or related discipline
• 2-5 years' experience as a QC analyst/chemist in a GMP environment
• Experience and familiarity with analytical testing equipment and methodology including HPLC, Karl Fischer, Spectrophotometry (UV/VIS), and LCMS