Full-Time
Quality Control
Chemist
Integrated Resources
501-1,000 employees
No salary listed
Urbana, IL, USA
In Person
Category
 Biology & Biotech (2) |
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Requirements
- Experience in scheduling, setting up and performing assays according to established protocols
- Ability to review protocols and determine chemicals and quantities needed
- Ability to perform procedures independently, accurately and safely according to established protocols
- Ability to interpret results and prepare complete, accurate records
- Ability to complete required volume of work to meet group/departmental goals and deadlines
- Ability to prepare written procedures as needed
- Capability to perform non-routine assays and assist in troubleshooting; apply a logical approach to basic problem solving and develop basic experimental design
- Understanding of techniques and instrumentation to ensure accurate analysis
- Ability to maintain lab supplies and order reagents as needed
- Ability to maintain and calibrate equipment, document and report overdue calibrations
- Ability to maintain a clean work area and properly dispose of waste
- Ability to document deviations from procedures and to notify supervisor
- Ability to utilize quality documentation systems for recording maintenance, calibration and usage of equipment and instruments
- Ability to label chemicals and reagents with all required quality documentation
- Ability to complete required quality training
- Ability to write and review drafts of quality procedures as directed by supervisor
- Ability to record quality observations in databases as directed by supervisor
Responsibilities
- Schedule, set-up and perform assays according to established protocols
- Review protocol and set-up assays according to priority level; determine chemicals and quantities needed; use appropriate equipment
- Perform procedure independently, accurately, in a safe manner, according to an established protocol; make minor adjustments to the protocol as needed
- After completion of assay, discard waste appropriately; return reagents to proper location and clean area
- Accurately interpret results and prepare complete, accurate and legible records
- Complete volume of work required to achieve group/departmental goals and meet established deadlines
- Prepare written procedures as needed
- Perform non-routine assays and assist in the troubleshooting process to resolve problems
- Carry out non-routine assays according to performance requirements for routine assays
- Use a logical approach to basic problem solving and demonstrate the ability and technical knowledge to develop a basic experimental design
- Understand techniques and instrumentation to ensure accurate analysis
- Contribute to support function of the Laboratory
- Ensure that lab supplies are adequately stocked
- Prepare testing reagents (e.g. buffers, gels, standards, etc.) as needed
- Maintain (clean, calibrate, etc.) equipment, properly document and notify appropriate individuals if calibration is overdue
- maintain a clean work area and properly dispose of waste
- Perform other group responsibilities thoroughly and in a timely manner
- Quality Expectations: Ensure worksheets and other quality documents accurately reflect current procedure. Document procedures with appropriate technical detail in writing as directed by supervisor
- Notify supervisor of any deviation from current procedure
- Utilize system of quality documents for recording maintenance, calibration and usage of equipment and instruments as directed by supervisor
- properly label chemicals and reagents with all needed quality documentation
- properly label chemicals and reagents with all needed quality documentation
- successfully complete required quality training
- Write and review drafts of quality procedures as directed by supervisor
- Record quality observations in databases as directed by supervisor to aid in quality improvement efforts
Company Size
501-1,000
Company Stage
N/A
Total Funding
N/A
Headquarters
Edison, New Jersey
Founded
1996
Simplify's Take
What believers are saying
- Certification boosts appeal to quality-focused healthcare organizations.
- Reskilling programs cut time-to-hire amid workforce shortages.
- Positions IRI among 15,000 Joint Commission-accredited elite firms.
What critics are saying
- Certification lapses in 12-18 months from failed onsite review.
- Patient complaints trigger decertification and client losses in 6-12 months.
- AMN Healthcare captures IRI's mid-sized clients in 12-24 months.
What makes Integrated Resources unique
- Joint Commission Gold Seal certifies IRI's staffing compliance since 2009.
- AI tool Nova hybridizes with reskilling to close healthcare skills gaps.
- Focuses on diversity hiring and performance monitoring for elite placements.
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Benefits
Wellness Program
Mental Health Support
Flexible Work Hours
Phone/Internet Stipend
Home Office Stipend
Conference Attendance Budget
Company News
Integrated Resources, Inc.
Jan 3rd, 2024
Edison, New Jersey - Integrated Resources Inc. has earned The Joint Commission's Gold Seal of Approval(R) for Health Care Staffing Services Certification by demonstrating continuous compliance with its performance standards.
Integrated Resources, Inc.
Feb 1st, 2023
Integrated Resources Inc. has earned The Joint Commission’s Gold Seal of Approval ® for Health Care Staffing Services Certification by demonstrating continuous compliance with its performance standards.