The PositionThis position is within the Quality Control structure, under the Quality Organization. An Associate Scientist III, Quality Control will support method validation and analytical testing pharmaceutical raw materials, in-process samples, finished drug substances and drug product, and/or stability sample testing activities for new drug substances and drug products. The Associate Scientist III is expected to perform several analytical techniques and make sound scientific decisions under guidance from management. All work is performed under GMP requirements. This position reports to QC Laboratory Management.
2nd shift work hours are 1 pm - 11:30 pm, Monday - Thursday, and includes a 10% shift differential.
Responsibilities- Performs routine analytical testing of pharmaceutical raw materials, in-process samples, finished products and/or stability samples using established test methods and procedures.
- Support method transfers and method validation activities.
- With guidance from laboratory leadership, works to meet project timelines and deliverables
- Ensures that training records are up to date and in compliance
- Perform a variety of analytical instrumentation (e.g., HPLC, GC, FT-IR, UV/Vis, KF, LCMS, Appearance, pH, Endotoxin etc.)
- Set up various instrumentations for testing according to written test methods with little to no supervision
- Performs analyses in a timely manner and communicate 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 review 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
- Embraces 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.
Wisconsin pay range
$80,000-$100,000 USD
Arrowhead provides competitive salaries and an excellent benefit package.
Candidates must have current, valid authorization to work in the country where this role is located.
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