QC Analyst

iS CLINICAL; Mesa (AZ); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

401k

Life

Dental

Vision

Health

PTO

Job summary

Innovative Skincare in Mesa, AZ is seeking a Quality Control Analyst to test raw materials, in-process batches, and finished products for GMP compliance. You'll perform laboratory analyses, maintain documentation, and ensure adherence to SOPs and safety procedures.

This on-site role requires a Bachelor's degree in Chemistry or related science and 1–3 years of GMP-regulated laboratory experience. You will calibrate equipment, record results, and collaborate with QC/QA and Production teams to

Qualifications

• Bachelor’s degree in Chemistry, Biology, or related science required.
• 1–3 years of laboratory or QC experience in GMP-regulated setting preferred.
• Strong documentation and regulatory compliance knowledge.

Responsibilities

• Perform laboratory testing on raw materials, bulk, and finished products.
• Follow established methods, SOPs, and GMP requirements.
• Record, analyze, and report test results accurately.
• Maintain and calibrate lab equipment as needed.
• Document all work in lab notebooks, logbooks, and electronic systems.
• Report and help investigate any out-of-specification results.
• Support stability studies and related lab activities.
• Work with QC, QA, and Production teams to resolve quality issues.
• Maintain a clean, safe, and compliant laboratory environment.

Skills

Attention to detail

Documentation accuracy

Communication skills

GMP knowledge

Laboratory testing

Education

Bachelor's degree in Chemistry, Biology, or related science

Tools

pH meters

Viscometers

Spectrophotometers

Balances

Job description

Embark on an extraordinary journey with us at Innovative Skincare, home of the renowned iS CLINICAL cosmeceutical brand. We are not just about creating groundbreaking skincare products; we are about creating chemistry that extends beyond the lab – a dynamic synergy between our products and our people.

At Innovative Skincare, we believe in a unique formula: the perfect blend of professional expertise and cultural harmony. This philosophy fuels our brand’s continuous growth and empowers each member of our team. We are more than a company; we are a community bound by passion, dedication, and a deep love for what we do, crafting an atmosphere that is as vibrant and energizing as our products.

Who we are:

Discover a world where skincare innovation meets scientific excellence at Innovative Skincare, a globally acclaimed leader in high-performance cosmeceuticals. Our journey is rooted in the relentless pursuit of creating skincare products that are not only effective but transformative. At the heart of our brand is the iS CLINICAL line, renowned for its fusion of nature’s finest ingredients with cutting-edge science. We are driven by a deep understanding of skin biology and a passion for unlocking the secrets of skin health and rejuvenation.

About the role:

The Quality Control Analyst is responsible for testing raw materials, in-process batches, and finished products to ensure they meet company and regulatory standards. This role performs laboratory analyses, maintains accurate documentation, and follows all GMP, SOP, and safety procedures.

The position will be fully on-site and located at our new Mesa, AZ facility.

Duties/Responsibilities:

• Perform laboratory testing on raw materials, bulk, and finished products.
• Follow established methods, SOPs, and GMP requirements.
• Record, analyze, and report test results accurately.
• Maintain and calibrate lab equipment as needed.
• Document all work in lab notebooks, logbooks, and electronic systems.
• Report and help investigate any out-of-specification (OOS) results.
• Support stability studies, sample management, and related lab activities.
• Work closely with QC, QA, and Production teams to resolve quality issues.
• Maintain a clean, safe, and compliant laboratory environment.
• Perform physical, chemical, and/or microbiological testing using approved analytical methods and instrumentation.
• Prepare reagents, standards, and solutions required for testing procedures.
• Perform routine calibration, maintenance, and troubleshooting of laboratory instruments (e.g., pH meters, viscometers, spectrophotometers, balances).
• Review and approve test data and documentation for accuracy prior to batch release.
• Participate in method validation, verification, and transfer activities as assigned.
• Other duties as assigned.

Required Skills/Abilities:

• Bachelor’s degree in Chemistry, Biology, or related science required.
• 1–3 years of laboratory or QC experience in a GMP-regulated industry preferred.
• Knowledge of laboratory techniques, GMP, and regulatory requirements.
• Strong attention to detail and documentation accuracy.
• Good organizational, problem-solving, and communication skills.
• Ability to stand and walk for the majority of the scheduled shift (typically 8-10 hours) while performing testing at laboratory benches and equipment stations, with only standard meal and rest breaks; this is an essential function of the role.
• Ability to frequently lift and carry sample containers, reagents, and laboratory supplies weighing up to 40 lbs.
• Ability to bend, reach, and twist to access lab benches, equipment, storage shelving, and sample refrigerators or freezers at varying heights.
• Manual dexterity and fine motor control sufficient to operate laboratory instruments, pipettes, and glassware, and to perform precise sample preparation and testing.
• Near vision sufficient to read instrument displays, labels, sample identifiers, and test documentation with precision; ability to distinguish colors as needed for certain analytical tests.
• Hearing sufficient to detect equipment alarms and communicate with laboratory and production staff.
• Ability to safely work with and around laboratory chemicals, reagents, and solvents, following proper handling and safety data sheet (SDS) guidelines.
• Ability to tolerate exposure to laboratory chemical odors, varying temperatures, and equipment noise.
• Ability to wear required PPE for the full shift, including safety glasses or goggles, lab coat, gloves, and closed-toe footwear, plus additional PPE (e.g., respirator) as required for specific testing.
• Compliance with all GMP, SOP, and plant safety/OSHA requirements.

Our company is dedicated to providing equal employment opportunities and embraces diversity and inclusion in our workplace. All eligible candidates will be considered for employment without bias towards their race, ethnicity, religion, gender, gender identity or expression, sexual orientation, national origin, genetic information, disability, age, or veteran status.

Benefits:

• 401k
• Life
• Dental
• Vision
• Health
• PTO