About the job
- Hold a Bachelor’s degree or higher in a science-related field, with a preference for chemistry.
- Possess a minimum of 3 years of relevant experience in a pharmaceutical environment.
- Conduct analyses, inspections, and tests on products, raw materials, in-process materials, packaging materials, and quantitative assays on samples to guarantee that quality standards align with company policies, customer expectations, and regulatory compliance.
- Execute a variety of qualitative tests and assays utilizing equipment ranging from standard analytical tools to advanced automated instrumentation, while assisting in the maintenance and certification of testing apparatus to ensure compliance.
- Perform essential inspections, checks, analyses, and documentation of studies.
- Compile and oversee quality statistics and reports.
- Utilize analytical instrumentation such as HPLC, GC, UV/Vis, KF, and FTIR for qualitative and quantitative analyses.
- Employ electronic laboratory information systems such as LIMS and Empower for data acquisition and processing.
- Have a foundational understanding of USP, cGMP, and FDA regulations.
- Demonstrate knowledge and experience within the field while still acquiring advanced skills and knowledge.
- Address a range of straightforward problems effectively.
- Analyze potential solutions using established procedures.
- Receive moderate guidance and direction in responsibilities.

