Quality Control Chemist

Integrated Resources, Inc ( IRI ); United States; On-site; USD 60,000 - 90,000; Full time

Job summary

Integrated Resources, Inc (IRI) seeks an analytical chemist to perform routine and non-routine chemical testing of samples per established methods. You will use HPLC, GC, UV-Vis, IR, and other instruments, and work with LIMS/Empower to process data.

The role requires knowledge of GMP and GLPs, data integrity, and contribution to investigations and continuous improvement in a fast-paced QC lab.

Qualifications

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

Responsibilities

• Perform routine and non-routine chemical testing of samples per written methodology.
• Analyze data using analytical instrumentation such as HPLC, GC, UV-Vis, IR, Particle Size Analyzer, KF Auto titrator, Bulk Density, and other QC instruments.
• Utilize LIMS and Empower for data acquisition and processing.
• Analyze data against specifications and notify management of any OOS and aberrant results.
• Contribute to root cause investigations and CAPA for corrective actions.
• Perform routine maintenance on lab equipment as needed.
• Provide peer review of laboratory testing as required.

Skills

Wet chemistry techniques

Education

BS or higher in science related discipline, chemistry is preferred

Tools

HPLC

GC

UV-Vis

IR

Particle Size Analyzer

KF Auto titrator

Bulk Density

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