Infotree Global Solutions
Specialist Quality Control (ELN/LMES/QC)
Infotree Global Solutions, Holly Springs, North Carolina, United States, 27540
Specialist Quality Control (ELN/LMES/QC)
Be among the first 25 applicants. Direct message the job poster from Infotree Global Solutions. Candidates should ideally be local, as onsite presence up to 50% may be required based on business needs. This position supports the QC ELN Project, including system validation/qualification deployment, eProcedure qualification, instrument report parsing script qualification, and master data templating related to Laboratory System Upgrade (CIMS (Reagent Manager)/LMES (Smart Lab eProcedure)). Lead eProcedure qualification in LMES supporting global QC method-specific eProcedure creation and qualification. Manage CIMS template creation for global QC reagents and client consumables. Provide incident management support as needed. Support application performance monitoring and label printing issues. Identify operational gaps and propose solutions. Assist in executing QC Laboratory Systems equipment integration across all client QC laboratories. Train client staff as each QC laboratory system goes live in production. Author, revise, and review SOPs, qualification reports, and technical reports. Lead planning, scheduling, and execution of daily QC Laboratory Systems activities. Top 3 Must-Have Skills:
Experience in implementing quality control systems in the pharmaceutical industry. Day-to-Day Responsibilities: Lead eProcedure qualification in LMES for client QC method-specific projects. Manage CIMS template requests for all client QC groups. Author, revise, and review documents supporting client QC systems (LMES/CIMS). Lead training workshops for client sites during system go-live. Seniority level
Mid-Senior level Employment type
Contract Job function
Manufacturing Industries
Staffing and Recruiting, Pharmaceutical Manufacturing
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Be among the first 25 applicants. Direct message the job poster from Infotree Global Solutions. Candidates should ideally be local, as onsite presence up to 50% may be required based on business needs. This position supports the QC ELN Project, including system validation/qualification deployment, eProcedure qualification, instrument report parsing script qualification, and master data templating related to Laboratory System Upgrade (CIMS (Reagent Manager)/LMES (Smart Lab eProcedure)). Lead eProcedure qualification in LMES supporting global QC method-specific eProcedure creation and qualification. Manage CIMS template creation for global QC reagents and client consumables. Provide incident management support as needed. Support application performance monitoring and label printing issues. Identify operational gaps and propose solutions. Assist in executing QC Laboratory Systems equipment integration across all client QC laboratories. Train client staff as each QC laboratory system goes live in production. Author, revise, and review SOPs, qualification reports, and technical reports. Lead planning, scheduling, and execution of daily QC Laboratory Systems activities. Top 3 Must-Have Skills:
Experience in implementing quality control systems in the pharmaceutical industry. Day-to-Day Responsibilities: Lead eProcedure qualification in LMES for client QC method-specific projects. Manage CIMS template requests for all client QC groups. Author, revise, and review documents supporting client QC systems (LMES/CIMS). Lead training workshops for client sites during system go-live. Seniority level
Mid-Senior level Employment type
Contract Job function
Manufacturing Industries
Staffing and Recruiting, Pharmaceutical Manufacturing
#J-18808-Ljbffr