Pharma QA Inspector – GMP & Packaging Excellence

PL Developments LLC

Piedmont (SC)

On-site

USD 55,000 - 70,000

Full time

5 days ago
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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 LLC, a leading manufacturer of OTC pharmaceutical products, seeks a QA Inspector to ensure products meet quality standards across production and packaging lines. The role emphasizes attention to detail, cGMP knowledge, and reporting discrepancies to maintain customer specifications.

On-site schedule: Monday to Friday 2:00pm-10:30pm with potential overtime as needed. The successful candidate will perform in-process checks, document findings, and support continuous improvement in

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.

Responsibilities

  • Inspect the initial product as it is bottled, checking accuracy of content, volume, bottle size, label verification, batch number, expiration date, and packaging specs.
  • Report errors or discrepancies to Line Leader, Supervisor, Director of Quality, or General Manager.
  • Perform in-process quality assurance checks during production runs per GMP and regulatory guidelines.
  • Review production logs in accordance with Good Documentation Practices.
  • Verify Line Clearances and review proper documentation; perform daily scale verification.
  • Assist in Process Validation as required.
  • Review and verify production kits before use, including components and labels.
  • Foster a culture of quality and continuous improvement, ensuring regulatory compliance.
  • Other duties as assigned.

Skills

Attention to detail
English communication
Minimal supervision
Basic math
Basic computer skills
Overtime capable

Job description

PL Developments LLC, a leading manufacturer of OTC pharmaceutical products, seeks a QA Inspector to ensure products meet quality standards across production and packaging lines. The role emphasizes attention to detail, cGMP knowledge, and reporting discrepancies to maintain customer specifications.

On-site schedule: Monday to Friday 2:00pm-10:30pm with potential overtime as needed. The successful candidate will perform in-process checks, document findings, and support continuous improvement in

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