Quality Control Analyst

ReviveRX is the premier licensed pharmacy specializing in health, wellness, and restorative medicine. We focus on treating the source, not just the symptoms, utilizing industry-leading technology. Collaborating with innovative pharmacists, healthcare providers, and pharmaceutical manufacturers, we provide personalized care. Our mission is to optimize treatment, revolutionize healthcare, and empower individuals to live vibrant lives. We welcome you to join us in our commitment to holistic wellness and personalized medicine.

Position Summary

The Quality Control Analyst is responsible for supporting microbiological and quality control testing activities, environmental monitoring, and cleanroom operations within a sterile compounding environment. This role executes routine microbiological testing, performs environmental and personnel monitoring, and ensures accurate documentation and data integrity in accordance with internal procedures and regulatory requirements.

The QC Analyst will also support sample preparation, coordination, and data review for assays such as potency and other analytical methods. The QC Analyst is expected to demonstrate a foundational understanding of both microbiological and analytical (chemistry) testing to support overall product quality.

Key Responsibilities

Perform and interpret microbiological and analytical testing activities, including but not limited to sterility, endotoxin, growth promotion, microbial identification, potency, and pH

Operate laboratory instrumentation and ensure accurate interpretation and documentation of analytical test results in accordance with established procedures

Perform raw material (API) sampling and ensure proper chain of custody for all samples

Perform, document, and interpret biological indicator incubation results to support sterilization monitoring

Conduct environmental and personnel monitoring (i.e., viable air, non-viable air, surface, and swab sampling) in classified cleanroom environments

Execute temperature, humidity, and differential pressure monitoring for controlled environments

Assist with incubation, tracking, and documentation of microbiological samples in accordance with SOPs

Support stability program activities, including sample management and coordination of testing

Maintain laboratory equipment and ensure proper operation

Complete, review, and maintain QC documentation, logbooks, and data records with accuracy and compliance

Investigate or support investigations of out-of-specification (OOS) results, environmental excursions, and nonconformances

Identify and assess quality risks in processes and escalate issues as needed

Assist in trending environmental monitoring data and identifying potential contamination risks

Support development, revision, and adherence to SOPs, protocols, and quality documentation

Collaborate with QA, Production, and Facilities to support contamination control and timely batch release

Perform other duties as assigned to support departmental goals, operational needs, and regulatory compliance

Required Qualifications

• Associate’s degree with relevant experience in a cGMP, GLP, or regulated laboratory environment.
• 3+ years of experience in a pharmaceutical, biotech, or compounding environment
• Experience with aseptic technique and cleanroom gowning
• Working knowledge of microbiological principles, aseptic technique, and contamination control
• Foundational understanding of analytical chemistry concepts, including sample preparation, laboratory instrumentation, and interpretation of analytical data
• Familiarity with cGMP/GLP documentation practice.
• Understanding of environmental and personnel monitoring programs
• Ability to follow and execute SOPs, protocols, and regulatory requirements
• Strong attention to detail with good organization and documentation practices

Proficiency in Microsoft Office Suite (Word, Excel, Outlook)

• Ability to interpret data and communicate results clearly
• Self-motivated and able to manage multiple tasks in a fast-paced environment
• Strong interpersonal, verbal, and written communication skills

Preferred Qualifications

• Bachelor’s degree in Microbiology, Biology, Chemistry, or related scientific field
• Experience with analytical chemistry methods (i.e., potency testing, HPLC, or similar)

Work Environment & Physical Requirements

• Primarily a controlled environment (ISO 5–8) and general office or laboratory spaces
• Frequent standing, walking, and use of hands
• Ability to lift up to 25 lbs
• Manual dexterity for handling small components and materials
• Use of PPE, sterile gowning, and adherence to strict contamination control protocols
• No makeup, perfume, fake or long nails, or fake eyelashes
• Schedule: Able to work flexible schedules and occasional weekends or holidays based on production needs

Featured Benefits

• Competitive salary
• Comprehensive health, dental, and vision insurance
• 401k with employer match

Paid Time Off

Employee Perks & Discounts

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