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Quality Control Associate Jobs in Merrillville, IN

AbbVie

Senior Associate, Quality Control

Chicago, IL · On-site +1

$84K/yr

Defines scope of quality control activities with the document author and the required source documents and data required. Conducts independent quality control review of documents per applicable ...

New

AbbVie

Senior Associate, Quality Control

Chicago, IL

Defines scope of quality control activities with the document author and the required source documents and data required. Conducts independent quality control review of documents per applicable ...

New

Testa Produce

Inventory Control Associate

Chicago, IL

$20/hr

Work with buyers on issues regarding product quantity, quality, and usage. * Provides inventory reports to buyers, AM warehouse managers, and the inventory control manager. * Operate a cherry picker ...

Testa Produce

Inventory Control Associate

Chicago, IL · On-site

$20/hr

Work with buyers on issues regarding product quantity, quality, and usage. * Provides inventory reports to buyers, AM warehouse managers, and the inventory control manager. * Operate a cherry picker ...

Quanta Services

Field Quality Lead I

Gary, IN · On-site

Two years of experience in a quality assurance / control role on an EPC project. * Associates degree in Construction Science or Construction Management. * Experience with Procore and its full suite ...

Quanta Services

Field Quality Lead II

Gary, IN · On-site

Associate's degree in a relevant field or a minimum of 4 years of experience in quality control/assurance or related field. * General understanding of quality inspections/audits and quality programs.

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Quality Control Associate information

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How much do quality control associate jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for quality control associate in Merrillville, IN is $24.98, according to ZipRecruiter salary data. Most workers in this role earn between $18.17 and $30.43 per hour, depending on experience, location, and employer.

What does a quality control associate do?

A Quality Control Associate is responsible for ensuring that products meet established standards of quality, including reliability, usability, and performance. They conduct inspections, perform tests, and document their findings to identify defects or deviations from specifications. Quality Control Associates often work closely with production teams to address issues and help maintain compliance with industry regulations. Their role is critical in maintaining customer satisfaction and upholding the reputation of their company. They may work in a variety of industries, including pharmaceuticals, manufacturing, and food production.

What are the key skills and qualifications needed to thrive as a quality control associate?

To thrive as a Quality Control Associate, you need a solid understanding of quality assurance principles, attention to detail, and often a background in science or manufacturing. Familiarity with inspection tools, laboratory equipment, and quality management systems (such as ISO standards) is typically required, and certifications like Six Sigma or ASQ may be advantageous. Strong analytical thinking, problem-solving abilities, and effective communication skills set exceptional candidates apart. These skills ensure that products consistently meet standards, reduce errors, and support overall operational excellence.

What are some common challenges quality control associates face when ensuring product consistency across different production batches?

Quality Control Associates often encounter challenges such as variations in raw material quality, changes in manufacturing processes, and tight production schedules that can lead to inconsistencies between batches. Addressing these issues requires keen attention to detail, effective communication with production teams, and a strong understanding of standard operating procedures. Staying proactive in identifying potential sources of variation and collaborating closely with other departments helps maintain high product standards and minimizes the risk of defects.

What is the difference between Quality Control Associate vs Quality Assurance Technician?

AspectQuality Control AssociateQuality Assurance Technician
CertificationsOften requires GMP, ISO, or industry-specific quality certificationsSimilar certifications, with focus on quality standards and compliance
Work EnvironmentLaboratory, manufacturing, or production settingsLaboratory, manufacturing, or quality compliance environments
Primary FocusInspecting products, testing samples, identifying defectsDeveloping and implementing quality systems, audits, and process improvements
Employer & Industry UsageManufacturing, pharmaceuticals, food productionManufacturing, pharmaceuticals, food industry

While both roles focus on quality, the Quality Control Associate primarily inspects and tests products to identify defects, whereas the Quality Assurance Technician develops and maintains quality systems to prevent issues. Both roles are essential in ensuring product quality and compliance within manufacturing and production environments.

What are the most commonly searched types of Quality Control jobs in Merrillville, IN?

The most popular types of Quality Control jobs in Merrillville, IN are:

What cities near Merrillville, IN are hiring for Quality Control Associate jobs?

Cities near Merrillville, IN with the most Quality Control Associate job openings:

Quality Control Associate jobs near you

Senior Associate, Quality Control

AbbVie

Chicago, IL • On-site, Remote

$84K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 3 days ago

New

AbbVie rating

8.7

Company rating: 8.7 out of 10

Based on 102 frontline employees who took The Breakroom Quiz

14th of 86 rated pharmaceutical

Job description

Company Description
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X and YouTube.
Job Description
Purpose:
The Strategic Medical Writing Operations Team is dedicated to delivering high-quality, scientifically accurate, and strategically aligned clinical and regulatory documentation that supports AbbVie's mission to transform the standard of care. Our team serves as a critical link between research, development, and regulatory submissions, ensuring clarity and compliance in all clinical and regulatory documents. We strive to innovate and enhance the processes of medical writing through cross-functional collaboration, agile methodologies, and the integration of cutting-edge technology, driving forward AbbVie's commitment to improving patient outcomes worldwide.
Responsibilities:
  • Defines scope of quality control activities with the document author and the required source documents and data required. Conducts independent quality control review of documents per applicable checklist by checking against source documents to ensure results are accurate.
  • Ensures quality control documentation is complete and accurate and uploaded to the master file per the established business processes.
  • Maintain strong knowledge of clinical regulatory documents requiring quality control review and business processes.
  • Mentors and provides guidance and training to less senior medical writing operations staff members. Provides management and oversight/supervision of 2 or more contractors as delegated.
  • Leads the development, implementation, and maintenance of medical writing operations business processes. Acts as subject matter expert (SME) for the master file system and quality control to the medical writing stakeholders.
  • Manages quality control outsourced to vendors that includes providing training and the preparation of the required documentation (e.g. clinical documents, checklists) for the quality control.
  • Effectively communicates quality control deliverables needed to stakeholders. Must demonstrate good interpersonal and organizational communication skills, including conflict management skills.

Qualifications
  • Bachelor's degree required. Bachelor's degree in Science, English, or Communication preferred.
  • 3-4 years in relevant industry experience in quality control/review of clinical regulatory documents or related experience in an area such as quality assurance, clinical research, drug development, medical writing, regulatory, or product support/R&D. Note: Higher education may compensate for years of experience. Years of experience may also compensate for lower education.
  • Project management experience is preferred.
  • Excellent knowledge of organization and content of clinical documents and eCTD structure. Knowledge of drug development and experience with Common Technical Document (CTD) content templates.
  • Working knowledge of global regulatory requirements and guidance associated with scientific publications or clinical regulatory document preparation and submissions. Competent/expertise in the application of business processes (guidelines, standard operating procedures, work instructions, job aids, etc).
  • Experience in being flexible with changing workload that requires prioritization and planning to support immediate/urgent business needs. Operations with limited oversight. Proven analytical and critical thinking skills.
  • Demonstrate higher degree of oral/written communication, interpersonal/organizational, analytical/critical thinking, and conflict management skills. Superior attention to detail and ability to prioritize multiple tasks/projects.
  • Experience in working with collaborative cross functional teams.
  • Demonstrate higher degree of proficiency, skill, and knowledge then more junior level. Computer literacy (hardware and software)/technical skills (ability to apply towards process improvements/operational efficiencies/automation).
  • Proficient skill and knowledge in Microsoft Office Products (Excel, OneNote, Outlook, PowerPoint, Project, SharePoint, Visio, Word) and Adobe in Windows operating system environment required. Proficient skills and knowledge in Microsoft document file formats (DocX) or other style file format tools, publishing software, and content management archival system(s) for eTMF/eSubmissions (Veeva Vault, CARA).

Additional Information
Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
  • The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.
  • We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
  • This job is eligible to participate in our short-term incentive programs.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company's sole and absolute discretion, consistent with applicable law.
AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more:
https://www.abbvie.com/join-us/reasonable-accommodations.html

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About AbbVie

Sourced by ZipRecruiter

AbbVie's mission is to discover and deliver innovative medicines that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas: immunology, oncology, neuroscience, eye care, virology, women's health, and gastroenterology, in addition to products and services across its Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube, and LinkedIn.

Industry

Scientific research and development services

Company size

10,000+ Employees

Headquarters location

North Chicago, IL, US

Year founded

2013

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