Quality Assurance Inspector - 2nd Shift

PL Developments Careers; Piedmont (SC); On-site; USD 42,000 - 54,000; Full time

Benefits offered by this job

Medical and Dental Benefits

Vision

401K with employer match

Group Life Insurance

Flex Spending Accounts

Paid Time Off and Paid Holidays

Tuition Assistance

Corporate Discount Program

Opportunities to Flourish Within the公司

Job summary

PL Developments, also known as PLD, is seeking a QA Inspector to ensure products meet established quality standards on the production line in Piedmont, SC. You will inspect bottles, verify labels, batch numbers and expiration dates per customer orders.

The role requires knowledge of cGMP, strong attention to detail, and the ability to report discrepancies. Work schedule is Monday to Friday, 2:00pm–10:30pm, with on-site duties and opportunities for overtime.

Qualifications

• Experience in Quality Assurance preferred.
• Excellent oral and written communication skills in English; fluency in Spanish is a plus.
• Basic knowledge and understanding of cGMP (current Good Manufacturing Practices).
• Ability to work effectively in a fast-paced environment.
• Basic math proficiency.
• Ability to work with minimal supervision.
• Able to work overtime when required.
• Basic computer skills.

Responsibilities

• Inspect the initial product as it is bottled, checking for accuracy in content, volume, bottle size, label verification, batch number, expiration date, and compliance with packaging specifications per customer purchase order.
• Report any errors or discrepancies to the Line Leader, Supervisor, Director of Quality, and/or General Manager.
• Perform quality assurance in process checks during production runs. This includes inspection, testing, and documentation, in accordance with Good Manufacturing Practices (GMP) and regulatory guidelines.
• Review production logs in accordance with Good Documentation Practices.
• Perform the verification of Line Clearances and review the proper documentation.
• Perform daily scale verification.
• Assist in Process Validation as required
• Perform the review and verification of the production kits (compounding and packaging) before being used, including sub-assembly components, labels, bottles, caps, master labels, master shippers, seals, lids, raw materials, etc.
• Drive a culture of quality and continuous improvement while fostering collaboration, accountability, and excellence in adherence to regulatory requirements and industry best practices
• Other duties as assigned.

Job description

513 Old Griffin Road
Piedmont, SC 29673, USA

• On-site
• Full-Time
• Requisition #: QUALI002702

Description

PL Developments, also known as PLD, is a leading manufacturer, packager, and distributor of over-the-counter (OTC) pharmaceutical products and consumer healthcare goods.

SUMMARY:

The QA Inspector ensures that all products meet established quality standards by inspecting items as they are produced and released from the production line. This role requires attention to detail, knowledge of cGMP, and the ability to report discrepancies, ensuring that products conform to customer specifications.

Work Schedule: Monday - Friday 2:00pm-10:30pm

JOB QUALIFICATIONS:

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

POSITION RESPONSIBILITIES:

• Inspect the initial product as it is bottled, checking for accuracy in content, volume, bottle size, label verification, batch number, expiration date, and compliance with packaging specifications per customer purchase order.
• Report any errors or discrepancies to the Line Leader, Supervisor, Director of Quality, and/or General Manager.
• Perform quality assurance in process checks during production runs. This includes inspection, testing, and documentation, in accordance with Good Manufacturing Practices (GMP) and regulatory guidelines.
• Review production logs in accordance with Good Documentation Practices.
• Perform the verification of Line Clearances and review the proper documentation.
• Perform daily scale verification.
• Assist in Process Validation as required
• Perform the review and verification of the production kits (compounding and packaging) before being used, including sub-assembly components, labels, bottles, caps, master labels, master shippers, seals, lids, raw materials, etc.
• Drive a culture of quality and continuous improvement while fostering collaboration, accountability, and excellence in adherence to regulatory requirements and industry best practices
• Other duties as assigned.

PHYSICAL REQUIREMENTS:

• Standing and walking for extended periods.
• Occasional lifting and overhead lifting.
• Reaching, pushing, pulling, bending, squatting, and climbing.
• Proper use of a step stool or ladder for inspection purposes.
• Comfortable working in environments with strong chemical odors and confined spaces.

BENEFITS:

PLD is a proud equal opportunity employer offering many corporate benefits, including:

• Medical and Dental Benefits
• Vision
• 401K with employer match
• Group Life Insurance
• Flex Spending Accounts
• Paid Time Off and Paid Holidays
• Tuition Assistance
• Corporate Discount Program
• Opportunities to Flourish Within the Company

PL Developments is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or veteran status.

Equal Opportunity Employer
This employer is required to notify all applicants of their rights pursuant to federal employment laws.For further information, please review the Know Your Rights notice from the Department of Labor.