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Drafting Quality Control Jobs (NOW HIRING)

Varite

Associate Quality Control

Holly Springs, NC · On-site

We are seeking a highly motivated and experienced Associate in Quality Control (QC) Chemistry to ... Draft, revise, and review technical and quality documentation such as SOPs, test methods, technical ...

anduril

Quality Control Supervisor

Ashville, OH · On-site

Experience with drafting and revising standard operating procedures and quality troubleshooting guides for inspection and quality control processes. * Experience with Manufacturing processes and ...

Endeavor 3D

Quality Control Technician

Douglasville, GA

$16.75 - $21.50/hr

A Quality Control Technician at Endeavor3D will play a pivotal role in maintaining the quality ... Experience drafting reports and collating data. * Knowledge and experience with computer programs ...

National Foods Packaging

QC Technician

Cleveland, OH · On-site

$20/hr

... quality control equipment prior to testing. • Conduct daily monitoring of Good Manufacturing ... draft reports, noting any relevant deviations from existing standards • Communicate quality or ...

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How much do drafting quality control jobs pay per hour?

As of Jun 5, 2026, the average hourly pay for drafting quality control in the United States is $20.97, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $23.08 per hour, depending on experience, location, and employer.

What is Drafting Quality Control?

Drafting Quality Control refers to the process of reviewing and verifying technical drawings, blueprints, and plans to ensure they meet established standards, specifications, and regulations. Professionals in this role check for accuracy, completeness, and compliance, identifying and correcting errors before the documents are released for construction or manufacturing. This process helps prevent costly mistakes, ensures quality outcomes, and maintains consistency across projects. Drafting Quality Control is essential in industries like architecture, engineering, and manufacturing, where precise documentation is critical.

What are some common challenges faced by Drafting Quality Control professionals and how can they be addressed?

Drafting Quality Control professionals often encounter challenges such as ensuring the accuracy and consistency of drawings across multiple projects, managing tight deadlines, and staying updated with evolving industry standards and software. Addressing these challenges involves implementing thorough review processes, maintaining clear communication with design and engineering teams, and regularly participating in training to keep skills current. Leveraging checklists and quality management systems can also help in identifying errors early and streamlining revisions.

What is the difference between Drafting Quality Control vs Drafting Technician?

AspectDrafting Quality ControlDrafting Technician
Primary RoleReview and ensure accuracy of technical drawings, adherence to standardsPrepare, modify, and produce technical drawings based on specifications
Required SkillsAttention to detail, knowledge of drafting standards, quality assuranceProficiency in CAD software, technical drawing skills, understanding of design concepts
Work EnvironmentQuality assurance departments, engineering firms, construction companiesDesign offices, engineering firms, manufacturing plants
CertificationsOften requires drafting or quality control certificationsTypically requires CAD certifications or technical diplomas

Drafting Quality Control focuses on reviewing and verifying drawings for accuracy and compliance, ensuring quality standards are met. Drafting Technicians are responsible for creating and modifying technical drawings. While both roles require technical drafting skills, Quality Control emphasizes review and standards adherence, whereas Technicians focus on production and drafting tasks.

What are the key skills and qualifications needed to thrive as a Drafting Quality Control specialist, and why are they important?

To thrive as a Drafting Quality Control specialist, you need a strong background in technical drawing, attention to detail, and knowledge of industry drafting standards, often supported by an associate's degree or relevant certification. Familiarity with CAD software (such as AutoCAD or SolidWorks) and quality management systems is typically required. Strong analytical skills, effective communication, and the ability to work collaboratively help ensure accuracy and consistency in project deliverables. These skills are essential for maintaining high drafting standards, reducing errors, and ensuring project compliance with specifications.

What are the 4 types of quality control?

In drafting quality control, the four main types are incoming inspection, process control, final inspection, and testing. These ensure that drawings, materials, and finished work meet specified standards and reduce errors. Effective quality control relies on documentation, skilled review, and adherence to industry standards.
Infographic showing various Drafting Quality Control job openings in the United States as of May 2026, with employment types broken down into 3% Locum Tenens, 3% As Needed, 11% Full Time, 57% Part Time, and 26% Contract. Highlights an 76% Physical, 7% Hybrid, and 17% Remote job distribution, with an average salary of $43,612 per year, or $21 per hour.
Quality Control Analyst

Quality Control Analyst

Mallinckrodt Pharmaceuticals

Madison, WI • On-site

$24.25 - $32.50/hr

Full-time

Posted 9 days ago

Mallinckrodt rating

7.7

Company rating: 7.7 out of 10

Based on 7 frontline employees who took The Breakroom Quiz

45th of 71 rated pharmaceutical

Job description

Company Description

Who We Are:

Mallinckrodt Pharmaceuticals is a multibillion dollar specialty pharmaceutical company focused on our mission: Managing Complexity. Improving Lives. We provide medicines to address unmet patient needs, stemming from 150 years of using our unique strengths, experience and expertise to help improve people's lives. Discover how our rich history of innovation and patient-centered solutions has helped influence our vision for the future.

What We Do:

Our strong ability to master and manage complexity is the key component in making high-quality products that provide value for patients. Mallinckrodt's growing portfolio of specialty pharmaceuticals help treat a wide variety of health conditions. We invest in areas such as autoimmune and rare diseases; immunotherapy and neonatal respiratory critical care therapies; analgesics and hemostasis products. To see what sets Mallinckrodt apart, take a look at our distinctive approach to solving complex challenges with unique solutions.

What We Believe In:

People throughout the world count on Mallinckrodt products every day to help them lead healthier lives. That's why we proudly stand by the three values we have held for 150 years: to produce quality products with the utmost integrity and unparalleled service in order to better serve the patients, customers and communities in which we live and work. Explore the roles of our dedicated employees and our commitment to responsibility.

At Mallinckrodt Pharmaceuticals, our five Cultural Hallmarks guide our work and serve as a foundation for our success. Employees are Accountable, Competitive, Collaborative, High Performing and Trustworthy.Our Culture

  • ACCOUNTABLE - We are each personally responsibility for ensuring Mallinckrodt's success
  • COMPETITIVE - We value breakthrough thinking that leads to industry leadership
  • COLLABORATIVE - We work together to create solutions
  • HIGH PERFORMING - We deliver on our commitments
  • TRUSTWORTHY - We consistently model our values
Job Description

The Quality Control (QC) Analyst will work both independently and within a team to perform daily analysis of in-process samples, finished product and raw materials via established test methods while following cGMP and GDP in the QC laboratory.  Typical analysis consists of pH, Osmolality, ELISA, PCR, sterility, UV/Vis spectroscopy and other general chemical and bioanalytical assays.

Principal Responsibilities

  • Conducts routine analysis of in-process samples, finished products, and raw materials according to standard operating procedures (SOPs) and Master Specifications.
  • Utilizes proper aseptic technique during the execution of analysis.
  • Performs stability testing according to established schedules.
  • Documents and investigates any OOS results.
  • Follows cGMP and GDP to perform all tasks.
  • Documents and assesses data against established specifications.
  • Perform inventory, stock and clean QC laboratories.
  • Perform QC review of data records.

Department specific/Non-essential responsibilities:

  • Assist with calibrating and maintaining laboratory equipment.
  • May perform training of new and existing QC team on established methods and procedures
  • May provide technical expertise for method optimization, verification, qualification, and validation.
  • May develop and qualify testing methods and SOPs.
  • May assist with or lead QC projects for process improvements.
  • May draft reports, plans and protocols.
  • May revise and updates SOPs.
  • Additional duties as assigned.
Qualifications

Experience / Skills:

  • Bachelor's degree in a scientific discipline or equivalent and a minimum of three years' related experience required.
  • Knowledge of cGMP is required.
  • Must possess skills and knowledge of general chemical and bioanalytical test methods.
  • Knowledge of ELISA, PCR, UV/Vis spectroscopy, cell culture and aseptic technique is preferred.

Competencies:

  • Attention to detail: able to organize and maintain data and information.
  • Ability to work in a controlled environment with gowning/PPE requirements.
  • Ability to learn through observation and hand's on experience.
  • Ability to work independently in a fast-paced, team oriented organization.
  • Strong written and verbal communication skills.
Additional Information

Organizational Relationship/Scope:

  • Reports to Quality Control leadership team.
  • Work is performed within a team of QC Analysts.
  • Regular communication with QC, manufacturing, technical operations among others.

Working Conditions:

  • 70% laboratory and manufacturing environment
  • 30% normal office and meeting room conditions
  • Must be able to perform work while aseptically gowned with the appropriate PPE

All your information will be kept confidential according to EEO guidelines.

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