Quality Technician

Aphena Pharma Solutions•Easton, MD

14d•$18 - $22•Onsite

About The Position

Aphena Pharma Solutions is looking for an Experienced Quality Technician to join our team! We are a dynamic pharma solutions provider specializing in contract packaging, repackaging, and manufacturing. If you have a keen eye for detail and a passion for quality, we want you on our team!

Requirements

PC proficient – Strong knowledge of Microsoft Word & Excel
GMP & ISO Knowledge – Understanding of FDA Good Manufacturing Practices & ISO standards
Strong organizational skills – Ability to prioritize assignments & manage multiple projects
Excellent communication skills – Ability to interact with vendors, customers, and all levels within the organization
Detail-oriented & analytical – Strong problem-solving and troubleshooting abilities
Ability to read & interpret drawings, templates, and technical documentation
Experience in Quality Control – Previous work with pharmaceuticals or medical devices preferred
Dependable, energetic, and self-motivated
Works well under pressure and with minimal supervision
Trustworthy and detail-oriented
Flexible and able to prioritize tasks effectively
Must be able to lift and move materials up to 50 lbs
Good visual awareness required
High school diploma required
Previous experience with GMP regulations in pharmaceuticals or medical devices
Proficiency in Microsoft Word, Excel, and the Internet
Strong problem-solving skills for complex, multi-layered issues

Nice To Haves

Knowledge of Statistical Process Control (SPC)
Ability to flowchart and graph data
Advanced coursework preferred

Responsibilities

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 & forms using Microsoft Word and Excel
Troubleshoot quality concerns on the production floor
Review & 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 & FDA GMP regulations
Perform data entry and retrieval using Aphena’s computer system
Support CAPA processes (Corrective & 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