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Sample Management Jobs in Ohio (NOW HIRING)

Olon USA LLC

QC Associate Scientist

Painesville, OH · On-site

Support stability programs through sample management, stability chamber monitoring, testing, and generation of stability data. * Coordinate timely and compliant generation of analytical data to ...

Lahlouh

Sample Administrator

Blue Ash, OH · On-site

The Sample Administrator is responsible for managing the end-to-end coordination of production samples within a print and mail environment. This includes collecting both internal and external samples ...

Lahlouh

Sample Administrator

Blue Ash, OH · On-site

The Sample Administrator is responsible for managing the end-to-end coordination of production samples within a print and mail environment. This includes collecting both internal and external samples ...

Certified Group

Sample Login Technician

Columbus, OH · On-site

$19.50/hr

JOB SUMMARY Process customer samples ensuring protocols are followed for receipt and handling ... Assisting with managing priorities and schedule such that individual goals as well as team goals ...

CatalYm GmbH

... reliably, samples are collected and processed according to protocol requirements, vendors are qualified, contracted, and managed effectively, and biomarker and bioanalytical deliverables are ...

Accenture

SAP Quality Manager - Life Sciences

Cleveland, OH · On-site

$64.75 - $84.25/hr

Design end-to-end SAP QM processes covering quality planning, inspection plans, inspection lots, results recording, usage decisions, quality notifications, sample management, certificates of analysis ...

Certified Group

Sample Login Technician

Columbus, OH

$19.50/hr

JOB SUMMARY Process customer samples ensuring protocols are followed for receipt and handling ... Assisting with managing priorities and schedule such that individual goals as well as team goals ...

Certified Group

Sample Login Technician

Columbus, OH · On-site

$19.50/hr

JOB SUMMARY Process customer samples ensuring protocols are followed for receipt and handling ... Assisting with managing priorities and schedule such that individual goals as well as team goals ...

TRIGA-S GmbH

Du arbeitest eng mit der Geschäftsführung sowie Kolleginnen und Kollegen aus Studienmanagement, Labor, Sample Management, Sales und Marketing zusammen * Du übernimmst Reporting, Pipelinemanagement ...

Frontage Laboratories

Scientist

Painesville, OH · On-site

Work with support teams including sample management, vivarium, QC, RW, PM & QA, BD as well as PIs and management. * Other duties as assigned. Education and Requirements : * B.S. in Toxicology ...

Solomon Page

Content Coordinator

Columbus, OH · On-site

$25/hr

Manage production documentation, including estimates, contracts, talent agreements, sample lists, and other shoot-related paperwork. * Coordinate the packing, shipping, tracking, receiving, and ...

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Sample Management information

See Ohio salary details

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How much do sample management jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for sample management in Ohio is $22.34, according to ZipRecruiter salary data. Most workers in this role earn between $16.68 and $22.64 per hour, depending on experience, location, and employer.

What is sample management?

A Sample Management job involves overseeing the receipt, storage, tracking, and distribution of samples in a laboratory or research setting. Professionals in this role ensure samples are properly labeled, documented, and stored under the correct conditions to maintain integrity. They also manage inventory, coordinate with researchers, and follow regulatory guidelines for handling and disposal. Attention to detail and organizational skills are essential in this role to ensure data accuracy and compliance.

What are the key skills and qualifications needed to thrive in sample management?

To excel in Sample Management, a strong background in laboratory procedures, attention to detail, and organizational skills are essential, often supported by a degree in life sciences or related fields. Familiarity with Laboratory Information Management Systems (LIMS), sample tracking software, and standard operating procedures is typically required. Excellent time management, communication, and problem-solving abilities help candidates stand out in this role. These competencies are vital as they ensure accurate handling, labeling, and distribution of samples, which underpin the reliability of scientific research and testing processes.

What are some common challenges faced in sample management, and how are they addressed?

A common challenge in Sample Management is maintaining accuracy when handling large volumes of samples and ensuring proper tracking to prevent mix-ups or loss. This is often addressed through the use of robust tracking systems and strict adherence to protocols. Team members typically collaborate closely with laboratory staff, quality assurance, and researchers to coordinate sample flows and troubleshoot any issues promptly. Staying organized and proactive helps minimize errors and ensures compliance with industry standards, making attention to detail essential for success in this role.

What are the most commonly searched types of Sample Management jobs in Ohio?

The most popular types of Sample Management jobs in Ohio are:

What are popular job titles related to Sample Management jobs in Ohio?

For Sample Management jobs in Ohio, the most frequently searched job titles are:

What job categories do people searching Sample Management jobs in Ohio look for?

The top searched job categories for Sample Management jobs in Ohio are:

Sample Management jobs near you
Infographic showing various Sample Management job openings in Ohio as of August 2026, with employment types broken down into 1% As Needed, 79% Full Time, 16% Part Time, and 4% Contract. Highlights an 80% Physical, 2% Hybrid, and 18% Remote job distribution, with an average salary of $46,468 per year, or $22.3 per hour.

QC Associate Scientist

Painesville, OH • On-site

Olon USA LLC
See more jobs at Olon USA LLCexternal

Full-time

Posted 4 days ago

Job description

Associate Scientist, QC

Department: Quality

Position Summary

We are seeking a detail-oriented and proactive Associate Scientist, QC to support quality control and stability testing activities within a cGMP-regulated pharmaceutical laboratory. This role is responsible for performing analytical testing of raw materials, in-process samples, finished products, and stability samples; generating and reviewing analytical data; supporting laboratory investigations; and ensuring compliance with applicable regulatory requirements. The ideal candidate will have experience working with small molecule drug substances and drug products in cGMP and GLP environments.

Essential Responsibilities

  • Perform analytical testing of raw materials, in-process samples, finished products, and stability samples using techniques such as HPLC, GC, KF, FTIR, XRD, DSC, TGA, PSD, NMR, ICP-MS, ICP-OES, and other laboratory instrumentation as required.
  • Support stability programs through sample management, stability chamber monitoring, testing, and generation of stability data.
  • Coordinate timely and compliant generation of analytical data to support client projects and manufacturing operations.
  • Review laboratory data for technical accuracy, completeness, compliance, and adherence to good documentation practices.
  • Conduct OOS, OOT, and laboratory investigations and support implementation of corrective and preventive actions (CAPAs).
  • Author and review protocols, reports, specifications, analytical methods, and related laboratory documentation.
  • Perform raw material sampling, testing, inspection, and coordination activities as required.
  • Manage laboratory inventory, retained samples, reagents, standards, chemicals, and associated laboratory systems.
  • Collaborate with Quality Assurance, Manufacturing, and Clients to support analytical testing, batch release, and stability studies.
  • Maintain compliance with cGMP, GLP, ICH, FDA, EMA, and other applicable regulatory requirements.
  • Other duties as assigned.

Qualifications

Education and Experience

  • Bachelor's degree in Chemistry or a related scientific discipline required.
  • Minimum of 3 years of related pharmaceutical analytical laboratory experience with a B.S. degree, or 1 year with an M.S. degree, or an equivalent combination of education and experience.
  • Relevant experience in a Quality Control laboratory is required.
  • Experience working in a cGMP and/or GLP-regulated environment is required.

Skills and Competencies

  • Proficiency with standard laboratory equipment, including HPLC, KF, XRD, PSD, analytical balances, pipettes, pH meters, and titration systems is required.
  • Experience with GC, FTIR, UV-Vis, DSC, TGA, IC, ICP-MS, and ICP-OES is preferred, but not required.
  • Experience with assay, impurity, raw material, and stability testing.
  • Familiarity with ICH stability guidelines and pharmaceutical quality systems.
  • Experience conducting OOS/OOT investigations and root cause analysis preferred.
  • Strong proficiency in Microsoft Word and Excel.
  • Strong written and verbal communication skills and the ability to work effectively with clients and cross-functional teams.
  • Ability to manage multiple priorities and work effectively in a fast-paced environment.
  • Strong understanding of chemistry principles, data analysis, and basic statistical concepts.