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Laboratory Testing Coordinator

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INW Phoenix Formulations

Tempe, AZ (In Person)

Full-Time

Posted 3 weeks ago (Updated 3 weeks ago) • Actively hiring

Expires 5/28/2026

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Job Description

Laboratory Testing Coordinator Tempe, AZ Job Details 17 hours ago Qualifications Safe work practices Record keeping Customer communication ISO standards Labeling Bachelor of Science Basic math Regulatory compliance Laboratory experience Laboratory information management systems English GMP Mid-level Improving operational efficiency Administrative experience Bachelor's degree Laboratory regulatory affairs Continuous improvement Task prioritization Organizational skills Productivity software 1 year Manufacturing Cross-functional collaboration Communication skills Regulatory compliance management Cross-functional communication FDA regulations Full Job Description This role will provide day-to-day coordination of laboratory sample flow and external testing activities to support operations, ensuring consistent oversight of sample intake, tracking, third-party laboratory coordination, and routing cross-functional communication. Support product release timelines, customer requirements, and regulatory compliance by serving as the primary administrative and communication contact between the lab, Sales, Quality and COA teams.
Essential Functions and Responsibilities:
To ensure that the organization has the operational resources to support the current demands as well as the plan for growth, this position will need to execute the following responsibilities as a minimum for successful performance. Coordinates intake, logging, labeling, storage, shipment, and tracking of laboratory samples, including raw materials, in-process materials, stability samples, and finished products. Acts as the primary contact for third-party ISO/IEC 17025-accredited laboratories by submitting samples, confirming testing requirements, tracking turnaround times, and following up on outstanding or delayed results. Provides routine status updates and communicates testing timelines and issues to internal teams, including Laboratory, Quality, Sales, and COA teams, to support product release and customer commitments. Receives and organizes Certificate of Analysis (COAs), performs administrative accuracy checks, and routes documentation to Quality for review and approval prior to release. Maintains laboratory testing records, external lab communications, and supporting documentation in accordance with internal procedures and FDA dietary supplement cGMP recordkeeping requirements. Prioritizes samples based on direction from Quality and business needs, including customer requests, investigations, stability programs, and release timelines, and assists with coordinating expedited testing when required. Supports continuous improvement efforts by identifying recurring issues, communication gaps, or delays related to sample flow and third-party testing. Assists with audit and inspection preparation by ensuring laboratory documentation, sample traceability, and third-party testing records are organized and available. Reports to work regularly. Perform duties safely and to report unsafe conditions or actions. Assists in other duties as needed and directed.
Minimum Qualifications:
B.S preferred Minimum of 1-3 years of experience in a laboratory setting Ability to read, write, and comprehend instructions and communicate effectively in English. Proficiency with Microsoft Office; familiarity with LIMS or electronic data systems preferred. Mathematical Skills including accuracy with arithmetic, decimals, and percentages. Skilled in organization, communication, detailed documentation, and adherence to SOPs with strong attention to detail.
Communication skills:
professionally interact and communicate with internal and external customers/vendors, laboratories. Strong ethics and integrity; process driven and quality-focused.
Preferred Knowledge, Skills, and Abilities:
Basic laboratory dexterity required for lab work, including handling media, plates, glassware, and biological materials. Ensure laboratory compliance with ISO and FDA requirements and obtain and maintain laboratory regulatory regulations. Ability to prioritize work and adjust priorities based on operation needs and urgency. Demonstrated analytical thinking, problem sensitivity, and problem-solving abilities. Knowledge of dietary supplement or food manufacturing, cGMP, FDA, USP, AOAC, and ISO laboratory requirements. Ability to work independently and collaboratively within a team environment. Skilled in monitoring, troubleshooting, critical thinking, process control, time management, following through, serving customers, and active listening. Work with a mindset of continuous process improvement, cost-reduction, improved efficiency with lab while maintaining customer satisfaction. Adhere to and promote proper practices and techniques which are consistent with current operating procedures, training requirements, safety practices and company policies.
Physical Demands :
Regularly required to stand, walk, and to sit for 3-4 hour intervals. Must occasionally lift up to 25 lbs. Specific sensory abilities required include near vision, manual dexterity, and ability to work with biological materials. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this job.
Pay Rate:
DOE Disclaimer:
Compensation reflective of candidate's experience. This job description is only a summary of the typical functions of the job, not an exhaustive or comprehensive list of all possible job responsibilities, tasks, and duties. The responsibilities, tasks, and duties of the jobholder might differ from those outlined in this job description and other duties, as assigned, may be part of the job. •Employment offers are contingent on successful completion of drug screen and background check•We are an EEO employer. We look forward to hearing from you!

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