Quality Assurance & Compliance Specialist in Tucson, Arizona at TMI ACQUISITION LLC

Quality Assurance & Compliance Specialist

About Tattoo Manufacturing International (TMI)

Tattoo Manufacturing International (TMI) is the world’s largest manufacturer of temporary tattoos, operating

out of its state-of-the-art facility in Tucson, Arizona. Founded in 1989, TMI has spent over three decades

pioneering safe, high-quality, and skin-friendly body art, producing millions of temporary tattoos daily for

distribution to over 80 countries. Beyond temporary tattoos, TMI leverages advanced printing, automation, and

in-house creative services to manufacture a broad range of promotional and consumer products, including

custom drink coasters, scratch-and-reveal items, magic paint sheets, activity booklets, and color-up kits.

Driven by a core commitment to safety, compliance, and American manufacturing, TMI serves as a trusted

global partner for retail, OEM, and private-label brands.

Role Summary: QA Compliance Specialist

The Quality Assurance and Compliance Specialist at TMI plays a pivotal role in safeguarding consumer

safety, product integrity, and regulatory alignment across all manufacturing and printing operations. Operating

at the intersection of production, R&D, and supply chain, this specialist is responsible for monitoring

compliance with global cosmetic, toy safety, and consumer product regulations (such as FDA, ASTM, and

EN71 standards) governing specialized inks, adhesives, and paper substrates. The role demands rigorous

oversight—from reviewing incoming raw material Certificates of Analysis (CoAs) and conducting quality

control testing, to investigating non-conformances and leading Root-Cause Analysis and Corrective and

Preventive Action (CAPA) plans. By authoring and maintaining audit-ready standard operating procedures

(SOPs), driving continuous process improvements, and training production floor personnel on Good

Manufacturing Practices (GMP), the QA Compliance Specialist ensures that TMI consistently upholds its

world-class reputation for safety, quality, and reliability.

Position Overview & Key Responsibilities

The Quality Assurance and Compliance Specialist ensures that all cosmetic and medical-grade temporary

tattoos, manufacturing processes, and operational procedures strictly adhere to global safety standards,

cosmetic regulations, and internal quality benchmarks.

Regulatory Compliance & Safety Standards: Monitor and enforce compliance with global cosmetic, toy

safety, and consumer product regulations (such as FDA regulations, EU cosmetic regulations, ASTM, and

EN71 standards) regarding inks, adhesives, and paper substrates used in temporary tattoo manufacturing.

Quality Control & Testing: Oversee routine testing of raw materials, colorants, medical-grade adhesives,

and finished tattoo sheets for skin safety, print clarity, durability, and adhesion. Inspect batches for defects

prior to packaging.

Corrective and Preventive Actions (CAPA): Investigate any production non-conformances, ink

formulation discrepancies, or customer quality feedback. Lead root-cause analyses and implement

effective CAPA plans to prevent recurrence.

Documentation & Standard Operating Procedures (SOPs): Author, maintain, and update SOPs, safety

data sheets (SDSs), batch records, and quality manuals. Ensure all compliance documentation is fully

audit-ready.

Supplier & Raw Material Verification: Review Certificates of Analysis (CoAs) for incoming pigments,

backing papers, and transfer films. Audit and vet external raw material suppliers to guarantee consistent

safety and quality inputs.

Staff Training: Train production, warehouse, and packaging personnel on quality control checkpoints,

Good Manufacturing Practices (GMP), and safety protocols specific to our manufacturing environment.

Continuous Improvement: Collaborate with production, research and development, and operations

teams to optimize manufacturing workflows, reduce waste, and enhance product safety and performance.

Qualifications & Requirements

Education: Bachelor’s degree in chemistry, Biology, Quality Management, Industrial Engineering, or a

related scientific/technical discipline.

Experience: 2 to 5 years of quality assurance or regulatory compliance experience within a regulated

manufacturing environment (cosmetics, consumer goods, medical devices, or specialty printing preferred).

Certifications: Certifications such as Certified Quality Auditor (CQA), Certified Quality Engineer (CQE),

or equivalent quality credentials are a plus.

Core Competencies: Working knowledge of cosmetic or consumer product safety regulations and Good

Manufacturing Practices (GMP); strong analytical and root-cause investigation capabilities; exceptional

attention to detail; and clear cross-functional communication skills