Packaging Associate – Powders

International Vitamin Corporation; Greenville, Northern (SC, KY); On-site; USD 30,000 - 36,000; Full time

Job summary

International Vitamin Corporation in Greenville, SC is seeking an entry-level packaging associate to perform basic bottle packaging tasks under GMP guidelines. You will inspect, weigh, label, and pack finished goods, ensuring compliance with quality standards and batch records.

You will support production, help train new staff, maintain cleanliness, and follow safety procedures. No prior experience required beyond 3–6 months in manufacturing preferred; strong English communication and

Qualifications

• High School Diploma or equivalent.
• 3–6 months manufacturing experience in a regulated environment preferred.
• Ability to read, write, and communicate in English.
• Knowledge of SOPs, Batch Records, and training documents.
• Basic math and computer literacy.
• Willingness to work overtime and be a team player.

Responsibilities

• Safely assist with bottle packaging line equipment (labeler, hopper, capper, bundler).
• Assemble cartons, apply labels, verify against work orders.
• Pack finished products, inspect lot numbers, labels, caps, neck bands.
• Perform rework and ensure corrective actions meet quality standards.
• Maintain cleanliness of tooling, machinery, and conveyors.
• Follow GMP/FDA regulations and company SOPs.
• Train and support new employees as needed.

Skills

Reading and writing in English

Strong work ethic

SOPs and Batch Records comprehension

Basic computer knowledge

Basic math

Team player

Willingness to work overtime

Education

High School Diploma or Equivalent

3–6 months manufacturing experience in regulated environment

Job description

Overview

Position Overview

Under the direct supervision of the Packaging Supervisor or Team Lead, this entry-level positionis responsible forperforming basic packaging operations in compliance with Good Manufacturing Practices (GMP). Key duties include inspecting,check-weighing, labeling, and packing finished products to ensure they meet quality and regulatory standards.

Responsibilities

Specific Responsibilities

Production Operations

• Safely and efficientlyassistwith all bottle packaging line equipment, including the labeler, bottle hopper,capper, and bundler.
• Assemble cartons, apply labels to cartons and shippers, and verify accuracy against the work order.
• Pack finished products while inspecting proper lot numbers, labels, caps, neck bands, and other quality criteria.
• Perform rework asrequiredand verify that all components are correct.
• Work efficiently to improve process reliability and minimize line downtime.
• Crosstrain and provide supportinother departments to meet business needs.
• Assistin training and mentoring new employees as needed.

Quality Assurance

• Verify all components, labels, and packaging against work orders.
• Inspect finished goods for proper lot numbers, caps, and neck bands.
• Perform rework and ensure all corrective actions meet quality standards.

Cleaning & Housekeeping

• Clean tooling, machinery, and conveyors after each run, including hoses, brushes, vibrators, and catch pans.
• Maintain general housekeeping by sweeping, mopping, and removing trash.
• Maintain a neat, clean, and safe workingenvironment always; promptly report any safety concerns, accidents, or injuries to a supervisor.

Safety & Compliance

• Understand andcomply withall GMP and FDA regulations, including gowning practices.
• Understand and adhere to all Company policies, procedures, SOPs, and Safety regulations.
• Promptly report any safety concerns, accidents, or injuries.

General Responsibilities

• Poses no direct threat to the health or safety of himself/herself, of others, or to property. Defined as a significant risk of substantial harm that cannot be eliminated or reduced to an acceptable level by reasonable accommodation.
• Requires regular attendance to perform essentialelementascontainedhereinbetween the assigned start and end times for work.
• Performs such individual assignments as management may direct.
• Other duties as assigned.

Qualifications

TheCandidate

Education,Experience, and Licenses

• High School Diploma or Equivalent OR passingIVCReading Comprehensionassessment
• 3-6 months manufacturing experience working in a regulated environment (cGMP or FDA) preferred

Knowledge, Skills, and Abilities

• Ability to read, write and communicate in English.
• Strong work ethic, professionalapproachand ownership of line production performance.
• Ability to read andcomprehendSOP’s, BatchRecordsand training documents
• Basic computer knowledge.
• Ability to understand basic math
• Strong work ethics,positiveattitudeand willingness to learn and develop new skills are a requirement.
• Teamplayer;workswell with others.
• Willingness to work overtime as needed.

International Vitamin Corporation (IVC) Is an Equal Opportunity Employer. Our organizationremainssteadfast in our commitment to fostering an inclusive and non-discriminatory work environment that welcomes individuals from all backgrounds. We firmlymaintainthe belief that every individual ought to be treated with respect and dignity, regardless of their race, color, religion, sex, sexual orientation, gender identity or expression, age, national origin, disability, veteran status, marital status, genetic information, or any other protected characteristic, as defined by the law. We pledge that all eligible job applicants shall receive an impartial and unbiased evaluation during the recruitment process, without any form of discrimination based on any of the protectedclass. Our dedication to promoting diversity and inclusivityremainsunwavering, and we take immense pride in cultivating a workplace culture that values and celebrates differences. Our efforts towards creating an environment that is free from prejudice and discrimination are an integral part of our organizational philosophy, and we stand committed to upholding theseprincipl