Associate Scientist III, Quality Control (2nd Shift)

Responsibilities

• Performs routine analytical testing of pharmaceutical raw materials, in-process samples, finished products and/or stability samples using established test methods and procedures.
• Supports method transfers and method validation activities.
• Works to meet project timelines and deliverables.
• Ensures that training records are up to date and in compliance.
• Performs a variety of analytical instrumentation (e.g., HPLC, GC, FT-IR, UV/Vis, KF, LCMS, Appearance, pH, Endotoxin etc.).
• Sets up various instrumentations for testing according to written test methods with little to no supervision.
• Performs analyses in a timely manner and communicates analytical or sample issues to senior staff and/or management.
• Works collaboratively with others.
• Show initiative and interest in learning new techniques and tests.
• Identify and troubleshoot analytical problems with instrumentation, general chemistry and computer applications.
• Maintain a clear, concise and accurate laboratory notebook or worksheet records.
• Peer reviews test data acquired by others, as applicable.
• Author technical documents such as OOS/atypical investigations, deviations and CAPAs.
• Demonstrate good written and verbal communication skills.
• Embrace cGMP requirements for all associated work.
• Remains flexible with changing priorities.

Requirements

• B.S. in Chemistry (or related field) with 3-5 years of relevant laboratory experience.
• Knowledgeable of cGMP laboratory requirements and operations.
• Familiar with analytical instrumentation, test methodology/validations, data acquisition systems, and typical cGMP policies and practices.

Qualifications

• Current, valid authorization to work in the country where this role is located.

Benefits

Arrowhead provides competitive salaries and an excellent benefit package.