eTeam
Pharmaceutical Talent Acquisition SME | eTeam
Hours are 2:00pm - 10:30pm. Local Candidates Only.
This position performs routine testing on all samples in the Analytical Services laboratory, providing analytical data for process control, quality control, process development, product development, and waste management. Employees will be required to work eight‑hour shifts, rotating days within the shift every three to four months. The CLIENT Quality Control lab is a 24‑hour production site that operates on three shifts.
Responsibilities
Perform routine analytical testing as directed by protocols and work instructions.
Work a variety of shifts, including weekends and holidays.
Request additional work to increase team productivity.
Prepare solutions, clean glassware, dispose of solid and liquid waste, and assist with overall laboratory operations.
Train others on waste management.
Alert lab leadership of issues or discrepancies involving sample integrity, supply inventory, safety concerns, or analysis irregularities.
Communicate troubleshooting opportunities in testing processes.
Conduct basic (operational) preventative maintenance according to work instructions.
Identify and communicate operational issues of laboratory instruments and equipment KPIs.
Operate Laboratory Information Management System (LIMS), Chromatography Data System (CDS), and other instrument‑specific computer systems.
Search various databases for test methods, specifications, and standards.
Promptly and accurately record, calculate, and report analytical results.
Review analytical data and various LIMS reports.
Communicate and discuss any issues with team members and supervisors.
Complete data entry for metrics and KPIs and identify process improvement ideas.
Assist in improving established procedures and implementing continuous improvement projects.
Communicate testing results to customers as required; act with customers in mind.
Notify leads when supplies/consumables are at critical levels.
Observe good safety and housekeeping practices.
Participate in lab/site safety programs and cross‑site initiatives.
Maintain knowledge of RCRA hazardous waste regulations, waste determinations, waste codes, and immediately communicate discovery of spills and leaks.
Required Qualifications
High school diploma plus a minimum of one year of laboratory experience.
Good oral and written communication skills.
High attention to detail and an ability to analyze outcomes against a standard.
Ability to diagnose typical instrument problems with little or no assistance and provide assistance to others.
Ability to multitask and prioritize workload to optimize laboratory efficiency and productivity.
Preferred Qualifications
Three or more years of laboratory experience.
Understanding of basic HPLC operations.
Seniority level Not Applicable
Employment type Contract
Job function Quality Assurance, Manufacturing, and Product Management
Industries Chemical Manufacturing, Pharmaceutical Manufacturing, and Biotechnology Research
Kansas City, MO
$18.00-$22.00
#J-18808-Ljbffr
This position performs routine testing on all samples in the Analytical Services laboratory, providing analytical data for process control, quality control, process development, product development, and waste management. Employees will be required to work eight‑hour shifts, rotating days within the shift every three to four months. The CLIENT Quality Control lab is a 24‑hour production site that operates on three shifts.
Responsibilities
Perform routine analytical testing as directed by protocols and work instructions.
Work a variety of shifts, including weekends and holidays.
Request additional work to increase team productivity.
Prepare solutions, clean glassware, dispose of solid and liquid waste, and assist with overall laboratory operations.
Train others on waste management.
Alert lab leadership of issues or discrepancies involving sample integrity, supply inventory, safety concerns, or analysis irregularities.
Communicate troubleshooting opportunities in testing processes.
Conduct basic (operational) preventative maintenance according to work instructions.
Identify and communicate operational issues of laboratory instruments and equipment KPIs.
Operate Laboratory Information Management System (LIMS), Chromatography Data System (CDS), and other instrument‑specific computer systems.
Search various databases for test methods, specifications, and standards.
Promptly and accurately record, calculate, and report analytical results.
Review analytical data and various LIMS reports.
Communicate and discuss any issues with team members and supervisors.
Complete data entry for metrics and KPIs and identify process improvement ideas.
Assist in improving established procedures and implementing continuous improvement projects.
Communicate testing results to customers as required; act with customers in mind.
Notify leads when supplies/consumables are at critical levels.
Observe good safety and housekeeping practices.
Participate in lab/site safety programs and cross‑site initiatives.
Maintain knowledge of RCRA hazardous waste regulations, waste determinations, waste codes, and immediately communicate discovery of spills and leaks.
Required Qualifications
High school diploma plus a minimum of one year of laboratory experience.
Good oral and written communication skills.
High attention to detail and an ability to analyze outcomes against a standard.
Ability to diagnose typical instrument problems with little or no assistance and provide assistance to others.
Ability to multitask and prioritize workload to optimize laboratory efficiency and productivity.
Preferred Qualifications
Three or more years of laboratory experience.
Understanding of basic HPLC operations.
Seniority level Not Applicable
Employment type Contract
Job function Quality Assurance, Manufacturing, and Product Management
Industries Chemical Manufacturing, Pharmaceutical Manufacturing, and Biotechnology Research
Kansas City, MO
$18.00-$22.00
#J-18808-Ljbffr