About Nexinfo:
NexInfo is a consulting firm focused on improving business processes and automation in the Supply Chain and Product Lifecycle Management sectors.We offer services in business process design, software implementations, managed services, staff augmentation, and SaaS solutions.We aims to help businesses across industries achieve their goals through industry best practices, lean process design,and advanced software solutions. Our ERP-related services address challenges such as inventory management,product lifecycle management, demand management, forecasting, sales and operations planning, business intelligence, security compliance, and financial alignment.
Job Title: Lab Tech - I
Location: MD - Frederick
Contract
Role: Execute tasks associated with sample management, shipment of samples, and other lab support QC functions, while interacting cross-functionally with personnel from other QC groups, Quality Assurance, Analytical Development, Manufacturing, Material Management (MM), and Corporate teams.
Responsibilities (include but are not limited to):
Receive incoming samples, verify documentation, and log sample information into LIMS.
Execute processes to support sample receipt and processing or aliquoting for release/stability testing and retains.
Label, store, and organize samples according to established procedures and storage requirements.
Coordinate sample transfers to internal and external testing labs.
Perform routine cleaning, maintenance, and restocking of sample storage areas.
Collaborate with MM, QA, and other QC functions including Corporate QC to support requirements around sampling, testing, and disposition.
Manage and complete all shipping activities within QC functions.
Complete routine review of records, such as sample chain of custody forms, processing logs, logbooks, and other documentation generated within QC Lab Support.
Assist with deviation and investigation activities as needed.
Provide updates during daily and weekly meetings.
Participate in Lean Lab and other Operational Excellence initiatives.
Comply with all safety, quality, and regulatory guidelines.
Perform other duties as assigned.
Basic Qualifications:
Bachelor s Degree OR
AA Degree and 2+ years experience working in Quality Control or biopharma laboratories preferably in an FDA regulated laboratory OR
High School Degree and 3+ years experience working in Quality Control or biopharma laboratories preferably in an FDA regulated laboratory.
Preferred Qualifications:
Strong knowledge in applying GMP in QC lab.
Exceptional attention to detail and ability to keep track of multiple ongoing projects
Proficient in Microsoft Office, Excel, Visio, and other related applications
Excellent interpersonal, verbal and written communications skills which are essential in this collaborative work environment
Comfortable in a fast-paces small company environment and able to adjust workload based on changing priorities.
Ability to be flexible with schedule, and work overtime as needed
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