Quality Technican

Now Hiring:
Experienced Quality Technician – Day Shift

Location: Easton, Maryland

Schedule: Monday – Thursday | 4 x 10‑hour shifts (6:30 AM – 5:30 PM)
Potential Mandatory Overtime on Fridays.

Pharmaceutical, OTC, Dietary Supplements, Animal Health, and Medical Devices

• Employee Medical Premiums: 75% paid by Aphena
• Medical Deductible: Partially covered by the company
• Company‑Paid Short‑Term Disability and Life Insurance
• 401(k) with Company Match
• PTO Accrual after 90 Days
• Paid Holidays and more!

• Inspect incoming components, in‑process products, and finished products based on specifications.
• Review documentation before production starts and perform First Piece Approval (FPA).
• Record and maintain data following Good Documentation Practices (GMP).
• Prepare inspection sheets and forms using Microsoft Word and Excel.
• Troubleshoot quality concerns on the production floor.
• Review and verify accuracy of all paperwork, including Device/Drug History Records (DHR).
• Ensure calibration of all inspection/test equipment and maintain accurate records.
• Investigate and gather data for customer complaints.
• Assist in process validations and maintain compliance with ISO and FDA GMP regulations.
• Perform data entry and retrieval using Aphena's computer system.
• Support CAPA processes (Corrective and Preventive Action Plans).
• Document and resolve non‑conforming materials and process discrepancies.
• Generate controlled labels and handle approvals/documentation.
• Maintain a clean and organized work area.

• PC proficient – Strong knowledge of Microsoft Word and Excel.
• GMP and ISO knowledge – Understanding of FDA Good Manufacturing Practices and ISO standards.
• Strong organizational skills – Ability to prioritize assignments and manage multiple projects.
• Excellent communication skills – Ability to interact with vendors, customers, and all levels within the organization.
• Detail‑oriented and analytical – Strong problem‑solving and troubleshooting abilities.
• Ability to read and interpret drawings, templates, and technical documentation.
• Experience in Quality Control – Previous work with pharmaceuticals or medical devices preferred.

• Knowledge of Statistical Process Control (SPC).
• Ability to create flowcharts.