Scientist II; Analytical Quality Development

Our Work Matters

At Kindeva we make products that save lives, ensuring better health and well-being for patients around the world.

The Impact You Will Make

In this role, you will develop, validate, and transfer analytical methods. You will support Production with investigations and cleaning validations, and assist Pharm Tech in the evaluation of APIs, excipients, and components. You will also collaborate with QC on analytical method optimization, analyst training, and laboratory investigations. Additionally, you will mentor junior chemists and write and review analytical methods, protocols, investigations, and reports.

ROLE RESPONSIBILITIES

• Identifies and implements improvements in analytical testing methods.
• Mentor and trains junior chemists in analytical methods and technologies.
• Performs method development and validation for analytical procedures.
• Executes method transfer and developmental protocols.
• Participates in new instrument qualification.
• Participates, examines and solves technical problems associated with the manufacture and handling of products and components
• Performs all activities under cGMP following company policies. Updates existing test methods. Also, writes and reviews analytical methods, protocol and reports

BASIC QUALIFICATIONS

• Minimum Bachelor degree in a science field with 5 years’ experience in GMP environment.
• Experience with analytical techniques like HPLC, GC/MS, LC/MS, FTIR preferred, familiarity with organic synthesis desired.
• Familiarity with EMPOWER software desired.

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