Quality Assurance Inspector / Pharmaceutical Packaging Job at Masis Professional Group, Bethlehem, PA

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  • Masis Professional Group
  • Bethlehem, PA

Job Description

QA Packaging Line Inspector – Direct Hire 2nd Shift

💼 Full-time | Excellent benefits | Amazing team culture

Join a happy, collaborative, and growth-focused team in a global pharmaceutical plant! We are seeking a QA Packaging Line Inspector to provide on-the-floor quality oversight for packaging operations.

🌟 What You’ll Do

  • Provide a quality presence on the packaging line.
  • Perform startup inspections , line clearance , and authorize start of runs .
  • Ensure in-line quality inspections , correct disposition of printed components, and proper destruction of unused materials.
  • Issue Master Batch Records , generate Bills of Materials (BOMs) , and verify correct components and materials.
  • Maintain, review, and control packaging batch records .
  • Accurately document in-process inspections and manage retain/customer samples.
  • Control finished goods status and labeling (Released, Quarantined, etc.).
  • Support special projects and assist with SOP updates related to packaging line QA activities.
  • Communicate issues affecting packaging, manufacturing, safety, or personnel to the appropriate managers.
  • Collaborate with production teams to resolve any quality concerns and support continuous improvement initiatives.
  • Willing to work overtime as needed and provide necessary mandatory coverage for the packaging line as necessary, may include some weekend coverage

🧠 Key Competencies

  • Strong critical thinking and root-cause analysis skills
  • Excellent communication skills across departments and levels
  • Professional, positive, and customer-focused demeanor
  • Creative problem solving; able to present multiple solutions
  • Energetic, enthusiastic, and motivational
  • Maintains confidentiality and demonstrates strong coaching skills.

🎓 Education & Experience

  • Associate degree in a science or technical field highly preferred .
  • 3+ years experience in QA or GMP-regulated manufacturing
  • Strong understanding of pharmaceutical cGMPs , regulatory requirements, and industry standards
  • Proficient in Microsoft Outlook, Excel, Word , plus experience with systems such as SAP and TrackWise
  • Excellent documentation practices; strong attention to detail and organizational skills
  • Ability to manage urgent requests with professionalism
  • Able to explain problems clearly and make recommendations

If you thrive in a fast-paced, collaborative environment and enjoy being on the production floor ensuring quality excellence, we’d love to meet you!

Apply today!

Job Tags

Full time, Afternoon shift,

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