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Materials Control Associate Jobs (NOW HIRING)

Grupo Canela Pvt Ltd

QC Associate

Pico Rivera, CA

$16 - $18/hr

We are seeking a QC Associate to join our team! You will conduct tests to determine the quality of materials and finished products as well as identify areas of improvement to increase efficiency.

Grupo Canela Pvt Ltd

QC Associate

Pico Rivera, CA

$16 - $18/hr

We are seeking a QC Associate to join our team! You will conduct tests to determine the quality of materials and finished products as well as identify areas of improvement to increase efficiency.

Sabert

Inventory Control Associate

Sayreville, NJ

$17.75 - $21.75/hr

* We are looking for an hourly Inventory Control Associate. Schedule isMonday to Friday 7 am - 3:30 ... Maintain raw material Inventory levels for manufacturing area * Supports facility maintenance and ...

VIVA USA INC

Inventory Control Associate

Joliet, IL · On-site

$16.50 - $20.25/hr

The Inventory Control Associate will report into the Finance Manager. In this position you will ... Associate's degree and at least 1 year of materials management experience OR At least 2 years of ...

Labcorp

Materials Control Worker

Chesapeake, VA · On-site

$17.75 - $27.69/hr

Labcorp is seeking a Warehouse Associate to join our team in Chesapeake, VA Work Schedule: Monday ... Maintain inventory control according to company standards * Participate in scheduled cycle counts ...

APN Software Services Inc

QC Associate

Tucson, AZ · On-site

Job title: QC Associate Duration: 12 months Location: Tucson, AZ The Quality Control Associate ... Responsibilities ● Perform inspection and testing of raw materials, in-process materials and ...

System One

Quality Control Associate

Oro Valley, AZ · On-site

$25.75/hr

Quality Control Associate Location: Oro Valley, AZ Type: Contract Compensation: $25.75/hr Work ... materials, in-process materials, and finished goods in a compliant manner. • Document test ...

Flux

QC Associate

Ashburn, VA · On-site

QC Associate The purpose of Quality Control Associate is to update and coordinate the planning ... Inspect incoming materials for submittal compliance and ensure that they are properly stored.

Fladger Associates

QC Associate

Fremont, CA · On-site

Excellent employment opportunity for a QC Associate III in the Fremont, CA area. * Performs ... Pulling and aliquoting raw material samples and distributing to the appropriate laboratories.

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Materials Control Associate information

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How much do materials control associate jobs pay per hour?

As of Jul 23, 2026, the average hourly pay for materials control associate in the United States is $22.56, according to ZipRecruiter salary data. Most workers in this role earn between $20.19 and $24.76 per hour, depending on experience, location, and employer.

What does a Materials Control Associate do?

A Materials Control Associate is responsible for managing the flow of materials within a company, ensuring that inventory levels are maintained and materials are available for production or distribution. They track shipments, receive and inspect incoming goods, and maintain accurate records in inventory management systems. Their work often involves collaborating with purchasing, production, and warehouse teams to support efficient operations and minimize delays. Attention to detail and organizational skills are essential for success in this role.

What are the key skills and qualifications needed to thrive as a Materials Control Associate, and why are they important?

To thrive as a Materials Control Associate, you need strong organizational skills, attention to detail, and experience with inventory management, typically supported by a high school diploma or equivalent. Familiarity with warehouse management systems (WMS), ERP software, and basic Microsoft Office applications is often required. Effective communication, teamwork, and problem-solving abilities are soft skills that help you excel in this role. These skills ensure efficient inventory flow, minimize errors, and support smooth operations within the supply chain.

What are some common challenges faced by Materials Control Associates, and how can they be managed effectively?

Materials Control Associates often face challenges such as inventory discrepancies, supply chain delays, and maintaining accurate records. Effective management involves diligent record-keeping, frequent communication with suppliers and internal teams, and proficiency with inventory management software. Staying organized and proactive in anticipating potential shortages or overstock situations is key. Collaborating closely with purchasing, production, and logistics departments ensures smooth operations and helps quickly resolve issues as they arise.
What cities are hiring for Materials Control Associate jobs? Cities with the most Materials Control Associate job openings:
What are the most commonly searched types of Materials Control jobs? The most popular types of Materials Control jobs are:
Materials Control Associate jobs near you
Quality Control Associate, Raw Materials

Quality Control Associate, Raw Materials

Capricor Therapeutics

San Diego, CA

$70K - $87K/yr

Full-time

Posted 6 days ago

Job description

Capricor Therapeutics (NASDAQ: CAPR) is a biotechnology company dedicated to advancing transformative cell and exosome-based therapies for rare diseases. At the forefront of our innovation is Deramiocel (CAP-1002), our lead cell therapy in late-stage development for Duchenne muscular dystrophy. We are also harnessing our proprietary StealthX™ exosome platform to unlock new possibilities in targeted delivery and vaccinology. Every program reflects our commitment to pushing the boundaries of science and delivering life-changing treatments to patients and families who need them most.

Position Summary 

The Quality Control Associate, Raw Materials is responsible for performing routine testing and documentation of raw materials used in Capricor’s manufacturing processes. This role ensures all incoming materials meet established specifications, regulatory requirements, and GMP standards. 

As part of the QC Raw Materials team, you will perform hands‑on laboratory work, maintain accurate and compliant documentation, support investigations, and collaborate with QC, QA, Procurement, and Manufacturing teams to ensure timely material readiness. This is a new headcount created to support the expansion of Capricor’s manufacturing and quality operations. 

 Team Mission 

The QC Raw Materials team ensures that all raw materials used in manufacturing consistently meet quality, safety, and regulatory standards. By verifying material identity, quality, and compliance, the team enables reliable production and supports Capricor’s broader mission of delivering high‑quality therapeutic products. 

 Responsibilities 

  • Perform routine quality control testing of raw materials in accordance with approved specifications and SOPs. 

  • Prepare samples, reagents, standards, and required materials for testing. 

  • Accurately document all test results in laboratory notebooks, forms, and electronic systems following GMP and data integrity standards. 

  • Identify, document, and report any out‑of‑specification (OOS), atypical, or questionable results to senior QC personnel. 

  • Support investigations, deviations, and CAPA activities as assigned. 

  • Maintain laboratory organization, cleanliness, and adherence to safety and GMP practices. 

  • Assist with equipment operation, calibration, routine checks, and maintenance. 

  • Follow all GMP, safety, and compliance procedures consistently. 

  • Collaborate with QC, QA, Manufacturing, and Supply Chain groups to ensure timely material testing and release. 

  • Participate in training, audits, and ongoing process improvement initiatives. 

Minimum Qualifications

  • Bachelor’s degree in Life Sciences, Chemistry, Biotechnology, or a related discipline. Will consider experience in lieu of education.

  • Associate I:  some laboratory or QC experience (academic or industry). 

  • Associate II: 1+ years of QC experience in a regulated environment (pharma, biotech, or manufacturing). 

  • Strong attention to detail and ability to follow SOPs and regulated procedures. 

  • Solid understanding of basic laboratory techniques, reagent handling, and instrumentation. 

  • Strong documentation skills and the ability to work efficiently with multiple samples and priorities. 

  • Familiarity with GMP or regulated laboratory environments. 

Preferred Qualifications

  • Working knowledge of GMP, quality systems, and raw materials workflows. 

  • Experience with analytical techniques such as FTIR, endotoxin testing, wet chemistry, or similar raw material identification methods. 

  • Experience with laboratory data systems (LIMS) and Microsoft Office programs. 

  • Strong communication skills and ability to work effectively in a team environment. 

Work Environment & Physical Demands

  • Laboratory‑based role with regular work in GMP areas. 

  • Prolonged periods of computer use for documentation, analysis, and reporting. 

  • Occasional lifting of materials or equipment up to 20 pounds. 

  • Ability to navigate laboratory and manufacturing support areas for sampling, inspections, and oversight duties. 

Compensation and Benefits

The posted salary range represents Capricor’s good-faith estimate of the salary range reasonably expected to be paid for this position at the time of hire. Final compensation will be determined based on job-related factors, including the candidate’s relevant experience, education, skills, certifications, scope of role, location, and internal equity.

This position may also be eligible for a discretionary annual performance bonus and, depending on the level of the role, long-term equity incentive awards in accordance with company policy.

Capricor Therapeutics offers a comprehensive benefits package that includes employer-sponsored medical, dental, and vision coverage; company-paid basic life and AD&D insurance; a 401(k) plan with company match; paid time off and company holidays; and paid parental leave. Additional voluntary benefits and wellness programs may also be available.

Why Capricor?

Capricor Therapeutics is advancing cell and exosome-based therapies with a focus on serious diseases where patients and families need new treatment options. Our work is grounded in scientific rigor, collaboration, and a shared commitment to moving meaningful therapies forward. Joining Capricor means being part of a mission-driven team working at the intersection of innovation, execution, and patient impact.

Come Work With Us

At Capricor, you’ll join a collaborative environment where employees are encouraged to contribute, grow, and help build the systems, science, and operations needed to support our next stage of growth. We value people who are thoughtful, accountable, hands-on, and motivated by work that can make a real difference.

Recruiting Fraud Notice

Capricor does not use Skype for interviews or recruiting activities. Candidates will only be contacted by someone using an official Capricor email address ending in @capricor.com. Capricor will never ask candidates to send money, deposit a check, purchase equipment, or provide payment for any reason as part of the recruiting or onboarding process.

Notice to Recruiting Agencies

Capricor Therapeutics does not accept candidate submissions or referrals from recruiting agencies, staffing firms, or third-party recruiters without express written approval from Talent Acquisition and a fully executed agreement with Capricor. Agencies that contact hiring managers directly, solicit business, or submit candidates without prior approval will not be considered for engagement. Any unsolicited submissions will become the property of Capricor Therapeutics, and no fees will be paid for candidates hired as a result of such submissions. We appreciate your cooperation and respect for this policy.