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Drafting Quality Control Jobs (NOW HIRING)

Aequor Inc

Associate Quality Control

Holly Springs, NC · On-site

Associate In Quality Control (Qc) Chemistry Fully onsite - standard hours - up to 5 days per month ... Draft, revise, and review technical and quality documentation such as SOPs, test methods, technical ...

Wallenius Wilhelmsen

Quality Control

Brunswick, GA · On-site

$20.50/hr

Maintain quality control records according to WW requirements. * Ensure accurate and timely ... Employees may encounter extreme temperatures, wetness, wind, fumes, dust particles and drafts.

Pacific Federal Management

GU · On-site

Collaborates with the leadership team across production departments and roles to draft acceptable ... Reviews quality control documentation such as checklists, logs, and reports for effectiveness ...

New

Wallenius Wilhelmsen

Quality Control

Brunswick, GA

$20.50/hr

Maintain quality control records according to WW requirements. * Ensure accurate and timely ... Employees may encounter extreme temperatures, wetness, wind, fumes, dust particles and drafts.

Aequor

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 ...

Samprasoft

Quality Control Analyst

Washington, DC · On-site

$27.25 - $36.50/hr

Senior Quality Control Analyst (Long-term Contract) Our large transportation-industry client based ... Support the team's processes to develop, review and edit draft policies and guidelines to align ...

CFL USA

Quality Control Technician

Adairsville, GA · On-site

$15.75 - $20.25/hr

We seek to hire a Quality Control Technician. The successful candidate will help establish and ... Evaluate data and draft reports, noting any relevant deviations from existing standards

Synthego

Quality Control Specialist

Redwood City, CA · On-site

$35 - $37/hr

Conduct first-pass data checks for accuracy, completeness, and compliance. * Assist in drafting ... in QC or a regulated analytical laboratory. * Ability to follow detailed SOPs and work with ...

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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.
Associate Quality Control

Associate Quality Control

Aequor Inc

Holly Springs, NC • On-site

Full-time

This job post has expired today. Applications are no longer accepted.

Job description

Associate In Quality Control (Qc) Chemistry

Fully onsite - standard hours - up to 5 days per month may require shift flexibility. Ideal candidate: B.S. and 3+YOE would be ideal in a chemistry lab environment. Position summary: We are seeking a highly motivated and experienced associate in quality control (qc) chemistry to support the startup and operational readiness of our qc laboratory. Working with minimal supervision, this individual will lead and contribute to critical activities including system qualifications, method transfers, and laboratory operations in a gmp-regulated environment.

Key responsibilities:

  • Collaborate cross-functionally with site teams to implement work order and preventative maintenance systems for laboratory equipment.
  • Review and contribute to validation documentation to support onboarding of equipment and computerized systems.
  • Draft, revise, and review technical and quality documentation such as SOPs, test methods, technical assessments, validation reports, trend reports, and safety evaluations.
  • Assist in the procurement of laboratory consumables and critical reagents required for startup activities.
  • Coordinate and execute training and method transfer activities for instruments including H/UPLC, TOC, conductivity, osmolality and other chemistry-based platforms.
  • Actively participate in audits, quality initiatives, and cross-functional projects with site or global impact.
  • Provide routine operational support during weekends and public holidays as required.

Preferred qualifications:

  • Bachelor's degree or higher in chemistry, compendial testing or a related scientific discipline.
  • Minimum of 4 years of relevant laboratory experience in a gmp pharmaceutical or biopharmaceutical manufacturing environment, with a strong background in analytical testing.
  • Proficient in analytical laboratory techniques and instrumentation.
  • Familiarity with laboratory systems such as LIMS and LMES/CIMS.
  • Demonstrated understanding of industry regulations, data integrity, and compliance standards.
  • Strong technical writing, documentation, and communication skills.
  • Experience with method validation, verification, and transfer.
  • Excellent interpersonal skills with the ability to collaborate across teams and adapt to varying communication styles.

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