Senior Analytical Chemist

Integrated Resources, Inc ( IRI ); United States; On-site; USD 65,000 - 90,000; Full time

Job summary

Integrated Resources, Inc (IRI) is seeking a skilled chemist to perform routine and non-routine chemical testing in a GMP-aligned lab. You will execute qualitative and quantitative analyses with HPLC, GC, UV-Vis, IR, and other QC instruments, and use LIMS and Empower to manage data and documentation.

The role requires familiarity with USP, cGMP, and FDA regulations, plus collaboration on investigations and continuous improvement efforts to uphold quality and safety.

Qualifications

• BS or higher in science related discipline, chemistry preferred.
• Wet chemistry techniques routinely used in QC testing.
• Familiarity with USP, cGMP and FDA regulations is expected.

Responsibilities

• Perform routine and non-routine chemical testing of samples following written methodologies.
• Conduct qualitative and quantitative analyses using analytical instrumentation (HPLC, GC, UV-Vis, IR, etc.).
• Utilize LIMS and Empower for data acquisition and processing; document results.
• Analyze data against specifications and report OOS or aberrant results to management.
• Support CAPA investigations and root cause analysis; participate in process improvements.

Skills

Wet chemistry

Data analysis

Team collaboration

Education

BS or higher in science related discipline

Tools

HPLC

GC

UV-Vis

IR

Particle Size Analyzer

KF Auto titrator

Bulk Density

LIMS

Empower

Job description

Candidates must have the following essential skill sets to be considered for the role:

• BS or higher in science related discipline, chemistry is preferred
• Wet chemistry techniques.

Job Description

• Perform routine and non-routine chemical testing of commercial, validation and stability samples in accordance to written methodology
• Perform qualitative and quantitative analyses using analytical instrumentation such as HPLC, GC, UV-Vis, IR, Particle Size Analyzer, KF Auto titrator, Bulk Density, and other routine QC instruments.
• Utilize electronic laboratory information systems such as LIMS and Empower for acquisition and processing of analytical data
• Analyze data products approved specifications, notifying management of any OOS and aberrant results
• Actively participate in root cause problem solving during laboratory investigations, provide input for effective corrective and preventive actions
• Perform routine maintenance on lab equipment, as needed
• Perform peer review of laboratory testing, as required
• Basic knowledge and understanding of USP, cGMP, and FDA regulations
• Create and maintain lab record documentation (notebooks and computer based) according to GMPs and GLPs
• Demonstrate the philosophy of Right First Time
• Maintain a clean and safe work environment and follow safety procedures and policies.
• Provide feedback on systems and processes to promote continuous improvement and champion selected changes
• Grow in the job, accountable for establishing and accomplishing annual personal development goals
• Contribute to department and site goals
• Communicate clearly and well within a team environment
• Participate in daily direction setting huddles to provide feedback and ensure alignment on daily/weekly/monthly objectives
• Shares information with others – keeping management informed and helping department to meet the goals
• Actively participate in regular one-on-one meetings with direct manager
• Communicate external to the department, where applicable
• Collaborate effectively to achieve team and organizational goals
• Prioritize assigned work to maximize time and equipment efficiency
• Work independently with limited supervision for routine assignments
• Troubleshoot problems encountered with methods and instruments - routinely solve, choosing among clearly defined alternatives
• Responsible for the accurate, timely and compliant execution of assigned projects, analytical testing and related documentation