What are the responsibilities and job description for the QC Technician II position at GOJO, Makers of PURELL?
Information about #31937 QC Technician II
Work Location: Wooster, OH USA
Shift: Third
Formulated to Care
For more than 75 years, GOJO, Makers of PURELL® has been powered by people who are energized by helping the world experience greater health and well-being.
The positive impact of our PURELL® hand and surface hygiene solutions is driven by our global community of highly collaborative and talented team members who love to learn, innovate, care for each other, and deliver our Purpose of Saving Lives and Making Life Better.
Role Objective
Provides routine and non-routine analytical testing and problem solving to support Supply Chain, Global Quality, and Research and Development (R&D).
Essential Functions And Responsibilities
Maintains a safe working environment and follows all safety procedures
▪ Quality of incoming materials and manufactured goods
▪ Provides accurate and timely communication of test results
▪ Maintains system of testing, analysis and results
▪ Participates in activities as assigned to improve a product or process or in response to customercomplaints
▪ Performs and/or provides support for process validation
▪ Performs and/or provides support for R&D, QA, Contract anufacturing, and Supply Chain
▪ Collects data for Game of Work Scorecards
▪ Maintains good housekeeping in work areas and performs assigned cleaning tasks
▪ Facilitates and/or implements standards and specifications
▪ Facilitates and/or implements test methods, procedures and analyses as needed
▪ Ensures hazardous wastes and other samples are properly contained and disposed of in accordance with GOJO policies and procedures
▪ Maintains laboratory supply inventory
▪ Washes and maintains glassware
▪ Overtime may be required
▪ Clean, maintain and prepare supplies and work areas
▪ Sets up, adjusts, calibrates, cleans, maintains, and troubleshoots laboratory equipment
▪ Revise/create procedures in Content Server
▪ Communicates quality issues, initiates Laboratory Investigation Reports (LIRs) and Quality Notifications (QNs)/Non-Conformance Events (NCEs), supports investigations, and ensures
dispositions of materials
Raw Materials Lab
▪ Participation on cross-functional New Product, Process or Problem-Solving Teams
▪ Collaboration with suppliers to resolve out of specification results on materials
▪ Ability to drive a tow motor vehicle
▪ Monitors hazardous waste satellite accumulation areas for compliance
Stability Lab
▪ Routinely provides support regarding customer complaints
▪ Collects and analyzes shelf life data for Annual Product Reviews (APRs)
▪ Creates, follows, and maintains the yearly stability matrix to ensure compliance with regulations
▪ Acquires and retains production samples from in-house and contract manufacturing required for shelf life testing
▪ Maintains environmental chambers and reserve storage areas
Analytical and In-Process Labs
▪ Audit production lines for compliance and quality
▪ Responsible for sampling water to prepare for analyses
▪ Analyze cleaning validation samples submitted to the labs
▪ Knowledge of the composition, structure, and properties of substances. This includes uses of chemicals and their interactions, danger signs, production techniques, and disposal methods.
▪ Knowledge of HPLC, UPLC, GC, TOC, FTIR, and other instrumentation functions/application
▪ Collects and analyzes water samples representative of that used for manufacturing product, research and development, and cleaning validation
Microbiology Lab
▪ Analyzes samples by means of Rapid Method Technologies, organism isolation/identification, membrane filtration and preservative effectiveness cycles
▪ Performs Total Plate Count and Enrichment studies using standard plating techniques
▪ Prepares and qualifies media including pH, sterility testing, and growth promotion testing
▪ Responds to situations that have a high potential for positive micro results and initiate action to minimize business risk
▪ Collects and analyzes water samples representative of that used for manufacturing product, research and development, and cleaning/rinsing for the presence of microorganisms
▪ Testing of non-woven personal care wipes products
▪ Captures and analyzes environmental samples
Education and Experience
Minimum of two (2) years of scientific education, prefer one year of college chemistry or biology and/or two (2) year work experience in Quality Assurance/Quality Control or in a GMP-manufacturing environment.
Competencies
Being Resilient
Collaborates
Cultivates Innovation
Customer Focus
Drives Results
Supervision/Coordination
This person will coordinate testing requirements and assignments needed to meet Supply Chain schedule. They will coordinate training of QC Temporary employees and new QC Technicians.
Role Type
Direct Manufacturing/Distribution - 100% On-Site
Physical Requirements
Manufacturing - Work Context Other
Travel Requirements
To Apply
To apply for this position, please complete the online application process. You will have an opportunity to include your resume and a cover letter. GOJO is an Affirmative Action/Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or status as an individual with a disability. Applicants must be lawfully authorized to work in the United States.
Recruiters, Search Agencies or others referring candidates to GOJO Industries, Inc. without written authorization from GOJO Industries, Inc. Human Resources will not be compensated in any way for their online referral even if GOJO Industries, Inc. hires the candidate. GOJO does not seek or respond to unsolicited resumes for positions that are not listed in the Careers section.
Work Location: Wooster, OH USA
Shift: Third
Formulated to Care
For more than 75 years, GOJO, Makers of PURELL® has been powered by people who are energized by helping the world experience greater health and well-being.
The positive impact of our PURELL® hand and surface hygiene solutions is driven by our global community of highly collaborative and talented team members who love to learn, innovate, care for each other, and deliver our Purpose of Saving Lives and Making Life Better.
Role Objective
Provides routine and non-routine analytical testing and problem solving to support Supply Chain, Global Quality, and Research and Development (R&D).
Essential Functions And Responsibilities
Maintains a safe working environment and follows all safety procedures
▪ Quality of incoming materials and manufactured goods
▪ Provides accurate and timely communication of test results
▪ Maintains system of testing, analysis and results
▪ Participates in activities as assigned to improve a product or process or in response to customercomplaints
▪ Performs and/or provides support for process validation
▪ Performs and/or provides support for R&D, QA, Contract anufacturing, and Supply Chain
▪ Collects data for Game of Work Scorecards
▪ Maintains good housekeeping in work areas and performs assigned cleaning tasks
▪ Facilitates and/or implements standards and specifications
▪ Facilitates and/or implements test methods, procedures and analyses as needed
▪ Ensures hazardous wastes and other samples are properly contained and disposed of in accordance with GOJO policies and procedures
▪ Maintains laboratory supply inventory
▪ Washes and maintains glassware
▪ Overtime may be required
▪ Clean, maintain and prepare supplies and work areas
▪ Sets up, adjusts, calibrates, cleans, maintains, and troubleshoots laboratory equipment
▪ Revise/create procedures in Content Server
▪ Communicates quality issues, initiates Laboratory Investigation Reports (LIRs) and Quality Notifications (QNs)/Non-Conformance Events (NCEs), supports investigations, and ensures
dispositions of materials
Raw Materials Lab
▪ Participation on cross-functional New Product, Process or Problem-Solving Teams
▪ Collaboration with suppliers to resolve out of specification results on materials
▪ Ability to drive a tow motor vehicle
▪ Monitors hazardous waste satellite accumulation areas for compliance
Stability Lab
▪ Routinely provides support regarding customer complaints
▪ Collects and analyzes shelf life data for Annual Product Reviews (APRs)
▪ Creates, follows, and maintains the yearly stability matrix to ensure compliance with regulations
▪ Acquires and retains production samples from in-house and contract manufacturing required for shelf life testing
▪ Maintains environmental chambers and reserve storage areas
Analytical and In-Process Labs
▪ Audit production lines for compliance and quality
▪ Responsible for sampling water to prepare for analyses
▪ Analyze cleaning validation samples submitted to the labs
▪ Knowledge of the composition, structure, and properties of substances. This includes uses of chemicals and their interactions, danger signs, production techniques, and disposal methods.
▪ Knowledge of HPLC, UPLC, GC, TOC, FTIR, and other instrumentation functions/application
▪ Collects and analyzes water samples representative of that used for manufacturing product, research and development, and cleaning validation
Microbiology Lab
▪ Analyzes samples by means of Rapid Method Technologies, organism isolation/identification, membrane filtration and preservative effectiveness cycles
▪ Performs Total Plate Count and Enrichment studies using standard plating techniques
▪ Prepares and qualifies media including pH, sterility testing, and growth promotion testing
▪ Responds to situations that have a high potential for positive micro results and initiate action to minimize business risk
▪ Collects and analyzes water samples representative of that used for manufacturing product, research and development, and cleaning/rinsing for the presence of microorganisms
▪ Testing of non-woven personal care wipes products
▪ Captures and analyzes environmental samples
Education and Experience
Minimum of two (2) years of scientific education, prefer one year of college chemistry or biology and/or two (2) year work experience in Quality Assurance/Quality Control or in a GMP-manufacturing environment.
Competencies
Being Resilient
Collaborates
Cultivates Innovation
Customer Focus
Drives Results
Supervision/Coordination
This person will coordinate testing requirements and assignments needed to meet Supply Chain schedule. They will coordinate training of QC Temporary employees and new QC Technicians.
Role Type
Direct Manufacturing/Distribution - 100% On-Site
Physical Requirements
Manufacturing - Work Context Other
Travel Requirements
To Apply
To apply for this position, please complete the online application process. You will have an opportunity to include your resume and a cover letter. GOJO is an Affirmative Action/Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or status as an individual with a disability. Applicants must be lawfully authorized to work in the United States.
Recruiters, Search Agencies or others referring candidates to GOJO Industries, Inc. without written authorization from GOJO Industries, Inc. Human Resources will not be compensated in any way for their online referral even if GOJO Industries, Inc. hires the candidate. GOJO does not seek or respond to unsolicited resumes for positions that are not listed in the Careers section.
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