Quality Assurance Technician 1st Shift

Blueroot Health INC.; Middletown (CT); On-site; USD 42,000 - 56,000; Full time

Job summary

Blueroot Health INC. is seeking a QA Technician to perform floor-level quality assurance across manufacturing and packaging. Responsibilities include in-process checks, line clearance, material verification, and ensuring proper labeling and storage conditions on the production floor.

The role requires familiarity with cGMP, GDP, and FDA 21 CFR Part 111, plus strong attention to detail and documentation practices. Prior QA/QC experience in dietary supplements, food, or pharma is preferred.

Qualifications

• High school diploma or GED required; associate or bachelor’s degree preferred.
• 1+ year of QA/QC or manufacturing experience in a cGMP-regulated environment preferred.
• Knowledge of cGMP, FDA 21 CFR Part 111, and GDP.
• Strong attention to detail with in-process checks and documentation.
• Experience with Excel; familiarity with eQMS or ERP/QMS platforms preferred.

Responsibilities

• Perform in-process checks and line clearance on manufacturing lines.
• Review and verify labels, material lot integrity and storage conditions.
• Conduct allergen swab testing and environmental monitoring as applicable.
• Maintain and document nonconformances and deviations.
• Assist with calibration logs, CAPAs, and other quality records.
• Carry out inventory control, FEFO, and label control on the floor.

Skills

Attention to detail

In-process inspections

Documentation

Quality Assurance

cGMP knowledge

Education

High school diploma or GED

Associate or Bachelor's in Biology, Chemistry, Food Science, or related field

Tools

Excel

eQMS

NetSuite

Job description

Description

PURPOSE STATEMENT:

The QA Technician performs floor-level quality assurance across manufacturing and packaging. This role executes in-process checks, line clearance and material verification, receiving and storage controls, label review, status labeling, and environmental and hygiene monitoring, and initiates quality records such as nonconformances and deviations. QA Technician responsibilities are shared between the Quality Assurance Team.

WHAT YOU'LL DO (MAJOR RESPONSIBILITIES):

• Logbook inspections
• Preventative maintenance monitoring
• Operation and verification of scales and balances (routine accuracy checks)
• Hygienic zoning monitoring
• Water and air supply testing (potable water, compressed air)
• Monitor gowning and hygiene compliance on the floor
• Perform in-process weight checks and inspections
• Random in-process AQL
• Authorizing bottling to continue runs; verify proper materials are used
• Raw material weighing & blending / dispensing verification
• Equipment cleaning verification and line clearance for each machine
• Internal audit assistance
• Review and approval of incoming product labels
• Receiving and controlled-storage program oversight (conditions, segregation)
• Status labeling of materials (quarantine/hold/release/reject tags)
• Monitor controlled storage conditions; inventory rotation (FEFO) and expiry (pick lists)
• In-process allergen swab testing
• Review service-vendor logs
• Initiate and document nonconformance reports and deviations
• Participate in day-to-day logs and trackers (calibration, PM, EM, complaints, deviations, CAPAs, training)
• Personal hygiene, dress code and visitor control / visitor logs
• Issuing records to bottling
• Inventory adjustments and status changes in NetSuite
• Repacking, relabeling, labeling of unlabeled bottle stock; producing unlabeled stock
• Carry out additional responsibilities as assigned to support departmental and organizational goals

WHAT YOU'LL NEED (KNOWLEDGE/SKILLS/EXPERIENCE):

• High school diploma or GED required; associate or bachelor's degree in Biology, Chemistry, Food Science, or a related scientific field preferred.
• One (1) or more years of experience in Quality Assurance, Quality Control, or manufacturing within a cGMP-regulated environment (dietary supplements, food, or pharmaceuticals) preferred.
• Working knowledge of current Good Manufacturing Practices (cGMP), FDA 21 CFR Part 111, and Good Documentation Practices (GDP).
• Strong attention to detail with the ability to perform in-process inspections, line clearance activities, and accurate documentation.
• Basic proficiency with Microsoft Office, including Excel; experience with electronic Quality Management Systems (eQMS), NetSuite, or similar ERP/QMS platforms is preferred.
• Ability to read, understand, and follow Standard Operating Procedures (SOPs), Batch Production Records (BPRs), and work instructions.
• Ability to work in a manufacturing environment and perform routine inspections while standing and walking throughout the production floor.

PHYSICAL REQUIREMENTS:

• Must be able to lift and/or move up to 50 pounds occasionally, with or without reasonable accommodation.
• Frequently stand, walk, bend, stoop, kneel, reach, and climb stairs throughout the workday.
• Perform repetitive hand and wrist movements associated with sampling, inspections, documentation, and use of quality equipment.
• Work safely around manufacturing equipment and moving mechanical parts.
• Visual acuity sufficient to inspect products, labels, packaging components, documentation, and equipment, including close vision, distance vision, color vision, peripheral vision, depth perception, and the ability to adjust focus.
• Work in a manufacturing environment with exposure to airborne powders, dust, noise, and common food or botanical allergens.
• Wear required personal protective equipment (PPE) and cGMP attire, including non-slip footwear, hair net, beard net (when applicable), face mask, gloves, and any additional PPE required for assigned areas.
• Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of the position.