Quality on the Floor Technician

The Quality On The Floor Technician is responsible for supporting Premier Research Labs’ commitment to producing extraordinary products by ensuring manufacturing processes are executed in compliance with established quality standards, GMP requirements, and internal procedures. This position serves as a daily quality presence on the production floor, verifying that product handling, documentation, labeling, line clearance, and process controls meet PRL expectations.
This role is highly visible and works cross-functionally with Production, Warehouse, and Quality teams to maintain compliance, prevent errors, and ensure product integrity from start to finish. This position supports PRL’s core values of Transformation, Extraordinary, and Community by reinforcing accountability, communication, and continuous improvement at the point of execution. Essential Functions
Manufacturing Floor Quality Oversight

• Provide real-time quality support on the manufacturing floor during blending, encapsulation, bottling, labeling, packaging, and related operations.
• Verify that manufacturing activities follow approved SOPs, batch records, and production instructions.
• Observe operations to identify risks, errors, or nonconformances and escalate concerns promptly.

Batch Record Review & Documentation Support

• Review manufacturing batch record entries in real time to ensure accuracy, completeness, and Good Documentation Practices (GDP).
• Identify documentation errors, omissions, or deviations and coordinate corrections per procedure.
• Support production personnel with proper documentation execution and compliance expectations.

Line Clearance & Changeover Verification

• Perform and document line clearance inspections prior to production startup and after product changeovers.
• Verify removal of previous labels, components, and product materials to prevent mix-ups and cross-contamination.
• Confirm correct product, label, lot number, expiration date, and packaging components are staged and approved for use.

Label & Component Verification

• Verify label issuance and correct usage on the line (right product, right lot, right label, correct artwork, correct placement).
• Ensure packaging components, inserts, and shipping materials meet defined requirements before use.
• Immediately escalate labeling concerns or misprints to Quality leadership.

In-Process Checks & Process Control Monitoring

• Perform and document in-process checks including (as applicable):
  • Weight checks
  • Fill volume verification
  • Tablet/capsule appearance checks
  • Seal integrity checks
  • Torque checks
  • Metal detector verification
  • Product count checks
• Ensure in-process checks are completed on time and documented correctly.

Sampling Support

• Collect and document in-process and finished product samples according to approved sampling plans.
• Maintain sample integrity and ensure samples are transferred properly to QC lab or retained as required.

Deviation / Nonconformance Identification

• Identify and document manufacturing nonconformances and process deviations.
• Support investigation activities by gathering information, observing process steps, and documenting findings.
• Assist with corrective action follow-up and verification when needed.

GMP & Housekeeping Compliance

• Enforce and support GMP requirements including sanitation, hygiene, PPE compliance, and controlled material handling.
• Monitor floor cleanliness and ensure workstations remain organized and inspection-ready.
• Ensure product is protected from contamination and improper handling throughout production.

Communication & Cross-Functional Collaboration

• Communicate directly with Production leadership regarding quality observations, corrective needs, and compliance issues.
• Partner with Warehouse and Production to ensure correct material status is maintained (quarantine, approved, rejected).
• Support daily production meetings or floor check-ins when requested.

Other Responsibilities

• Perform other duties as assigned by Quality leadership to support operational needs and business priorities.

Education & Experience

• High school diploma or GED required; Associate’s or Bachelor’s degree preferred.
• 1–3 years of experience in a manufacturing environment preferred (dietary supplement, food, pharmaceutical, or regulated industry strongly preferred).
• Experience with batch record documentation, labeling operations, packaging lines, or GMP environments strongly preferred.

Knowledge, Skills & Abilities

• Strong attention to detail and ability to detect errors before they become product issues
• Strong understanding of manufacturing flow, labeling practices, and material control concepts
• Ability to follow written procedures and enforce compliance expectations respectfully and professionally
• Strong communication skills and confidence working directly with production teams
• Ability to manage multiple tasks in a fast-paced manufacturing environment
• Comfortable working in production areas with equipment, noise, and frequent movement
• Proficient with basic computer skills and documentation systems (Word/Excel preferred)

Work Environment & Physical Requirements

• Work is performed primarily in a manufacturing environment onsite. 
• Must be able to stand and walk for extended periods.
• Must be able to lift and carry up to 40 pounds as needed.
• Exposure to powders, noise, machinery, and temperature variation may occur.
• Must be able to wear required PPE (hairnets, gloves, lab coats, masks, etc.).

Work Schedule

• Standard schedule is Monday–Friday, with flexibility based on production demands.
• Overtime may be required during peak production periods.