Electrolyte QA Inspector - Precision Bottling & Compliance

PL Developments LLC; Piedmont (SC); On-site; USD 42,000 - 64,000; Full time

Benefits offered by this job

Medical Benefits

Dental Benefits

401K with employer match

Paid Time Off

Job summary

PL Developments LLC in Piedmont, SC is seeking an Electrolyte QA Inspector to ensure products meet quality standards as they are produced and released from the line.

You will verify content, volume, bottle size, labels, batch numbers, expiration dates, and packaging specs, reporting discrepancies to supervisory staff.

The role follows a Sunday-Thursday 10pm-6:30am schedule, requires cGMP knowledge and accuracy, and offers benefits and opportunities within PLD.

Qualifications

• Previous experience in Quality Assurance preferred.
• Excellent oral and written communication in English; Spanish is a plus.
• Basic knowledge of current Good Manufacturing Practices (cGMP).
• Basic food safety knowledge; training provided as required.
• Ability to work effectively in a fast-paced environment.
• Basic math proficiency; ability to work with minimal supervision.
• Ability to work overtime when required.
• Basic computer skills.

Responsibilities

• Inspect the initial product as bottled for content accuracy, volume, bottle size, labeling, batch number, and expiration date.
• Inspect/verify initial product during compounding for correct components and food safety standards.
• Report errors or discrepancies to Line Leader, Supervisor, Director of Quality, or General Manager.
• Perform in-process QA checks during production, including inspection, testing, and documentation per GMP.

Skills

Quality Assurance

English fluency

cGMP knowledge

Food safety basics

Attention to detail

Basic math

Basic computer skills

Overtime willingness

Job description

PL Developments LLC in Piedmont, SC is seeking an Electrolyte QA Inspector to ensure products meet quality standards as they are produced and released from the line.

You will verify content, volume, bottle size, labels, batch numbers, expiration dates, and packaging specs, reporting discrepancies to supervisory staff.

The role follows a Sunday-Thursday 10pm-6:30am schedule, requires cGMP knowledge and accuracy, and offers benefits and opportunities within PLD.