Quality Assurance Technician 1st Shift

Socket.dev; Middletown (CT); On-site; USD 52,000 - 76,000; Full time

Job summary

Socket.dev is seeking a QA Technician to perform floor-level QA across manufacturing and packaging lines in Middletown, CT. You will conduct in-process checks, line clearance, label review, and material verification while maintaining environmental monitoring and hygiene practices.

You’ll document nonconformances, deviations and support CAPAs, audits, and training records, with duties spanning logbooks, QA checks, and controlled-storage oversight.

Qualifications

• 1+ year in QA/QC or manufacturing within a cGMP environment.
• Knowledge of cGMP, FDA 21 CFR Part 111, GDP.
• Detail-oriented with ability to perform inspections and documentation.
• Ability to read SOPs, BPRs and work instructions.
• Ability to work in a manufacturing setting, standing for long periods.

Responsibilities

• Perform floor-level QA checks and line clearance activities.
• Review incoming product labels and oversee controlled-storage program.
• Monitor hygiene, gowning, sampling and in-process testing.
• Maintain logs, calibration, CAPAs and training records.
• Assist in internal audits and vendor log reviews.
• Issue nonconformances and deviations as needed.
• Ensure FEFO inventory rotation and proper labeling.

Skills

Logbook inspections

Preventative maintenance

Scales & balances operation

Hygienic zoning monitoring

Water testing

Air testing

Gowning compliance

In-process weight checks

Allergen swab testing

CAPA tracking

Training records

Reviewing labels

Vendor log review

SOPs/BPRs reading

Education

High school diploma or GED

Associate degree in Biology, Chemistry, or Food Science

Bachelor’s degree in related field

Tools

NetSuite

eQMS

ERP/QMS platforms

Microsoft Excel

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.