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Raw Materials Testing Jobs (NOW HIRING)

seamancorp

Raw Materials Specialist

Wooster, OH · On-site

Monday through Friday, 7:00am to 4:00pm POSITION SUMMARY The Raw Materials Specialist will conduct raw material testing in support of quality and operational requirements. The Raw Materials ...

Talnt

Raw Materials Specialist

Akron, OH

$27 - $30/hr

Collect, label, and process samples for testing and evaluation according to approved procedures ... Experience in raw material inspection, quality control, inventory management, receiving, or ...

Pace

Senior Chemist- Raw Materials

Morrisville, NC · On-site

Performs intermediate to advanced analytical testing of raw materials using techniques such as HPLC, GC, FTIR, UV-Vis, titration, wet chemistry, and other instrumentation per SOPs, compendial methods ...

Carhartt

Director, Raw Materials Quality

Dearborn, MI · On-site

Manage and hold associates accountable for raw material testing, systems and audits. * Collaborates ... with Product Development to train and on-board new and current vendors regarding the fabric, trim ...

ALO

Raw Materials Developer, Accessories

Commerce, CA · On-site

$90K - $110K/yr

Technical Development and Testing * Establish material specifications and validate against ... Troubleshoot raw material issues such as delamination, cracking, peeling, color migration ...

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How much do raw materials testing jobs pay per hour?

As of Jun 7, 2026, the average hourly pay for raw materials testing in the United States is $22.20, according to ZipRecruiter salary data. Most workers in this role earn between $18.75 and $25.24 per hour, depending on experience, location, and employer.

What is the difference between Raw Materials Testing vs Quality Control Technician?

AspectRaw Materials TestingQuality Control Technician
CertificationsLaboratory certifications, quality assurance trainingQuality control certifications, industry-specific training
Work EnvironmentLaboratories, manufacturing plantsProduction lines, warehouses
Industry UsageMaterial suppliers, manufacturing companiesManufacturing, production facilities

Raw Materials Testing focuses on analyzing and verifying the quality of raw materials before production, ensuring they meet specifications. Quality Control Technicians monitor ongoing production processes to maintain product standards. While both roles require similar certifications and work environments, Raw Materials Testing is more specialized in initial material assessment, whereas Quality Control Technicians oversee the final product quality during manufacturing.

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What job categories do people searching Raw Materials Testing jobs look for? The top searched job categories for Raw Materials Testing jobs are:
Infographic showing various Raw Materials Testing job openings in the United States as of May 2026, with employment types broken down into 1% As Needed, 89% Full Time, 9% Part Time, and 1% Temporary. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $46,181 per year, or $22.2 per hour.
Senior Manager, Quality Control Raw Materials

Senior Manager, Quality Control Raw Materials

Beam Therapeutics

Durham, NC • On-site

Other

Posted 13 days ago

Job description

Position Overview:

The QC Manager, Raw Materials will be responsible for developing, leading, and managing the Raw Materials QC program at the Beam Therapeutics Manufacturing facility in Durham, NC. This role will develop and maintain documentation regarding testing requirements and strategies, serve as a subject matter expert (SME) for raw materials issues, providing technical expertise aligned with current GMPs and current industry practices. This person will have knowledge and experience with USP methods, and the ability to apply as required, and as well as maintaining compliance to USP, ICH and FDA guidance documents. Interface with Manufacturing, Supply Chain, and Quality Assurance leadership and participate and/or lead interdepartmental teams to address quality-related issues.

This role requires on-site presence and engagement. The position will report to the Quality Control Senior Director.

Primary Responsibilities:

  • Build and manage the raw materials QC program at the Beam Therapeutics Manufacturing facility.
  • Develop and maintain all documentation with regards to testing requirements and strategies, including material specifications.
  • Serve as a SME for raw materials issues, providing technical expertise aligned with current GMPs and current industry best practices.
  • Manage contract laboratories as needed.
  • Own and author risk assessments for raw material programs.
  • Support supplier change notifications and material enrollment.
  • Identify need for development of new assays with compendial and GxP requirements.
  • Accountable for managing the raw materials testing program to ensure quality, product specifications and adherence to all current GMPs, USP, ICH and FDA guidance documents.
  • Evaluate QC systems and recommend and/or implement system improvements.
  • Author technical protocols and reports for Raw Materials testing qualification, validation, or verification.
  • Author test methods and SOPs for the Raw Materials testing program.
  • Create, review, and approve out-of-specification (OOS) and out-of-trend (OOT) investigations, deviations, CAPAs, and Change Controls.
  • Manages release of raw materials used in manufacturing.
  • Provide oversight of material master data as it relates to inspection plans and material life cycle.
  • Maintain records and databases in accordance with procedures.
  • Hire and manage staff as needed.
  • Oversee management of in-house raw material test equipment.

Qualifications:

  • Bachelor's or advanced degree in biology, biochemistry or closely related scientific discipline.
  • At least 7-10 years of CGMP QC experience in a cell therapy/biotech/pharmaceutical setting is required.
  • Expert knowledge of pharmaceutical/biotech Raw Materials testing is required.
  • At least 3 years of management experience is required.
  • Basic knowledge of qualifications and validations; current industry practices; and strong experience with guidance interpretation and application.
  • Knowledge of cGMPs, ICH, USP, FDA requirements is required, including equipment and method validation/verification.
  • Experience with risk assessment tools is desired
  • Excellent critical thinking and technical writing skills.
  • Excellent interpersonal and communication skills to lead, facilitate and follow.
  • Computer skills required to use Microsoft Word, Project, Visio, and Excel programs.

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