Quality Technician

Quality Technician# Quality TechnicianHot JobLiquid and Topicals Division MD - Easton, MD 21601## OverviewSalary Range$18.00 - $22.00 HourlyLevelExperiencedPosition TypeFull TimeJob ShiftAnyEducation LevelHigh SchoolTravel PercentageNoneCategoryQA - Quality Control## Description### **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** **Industry:** Pharmaceutical, OTC, Dietary Supplements, Animal Health, & Medical DevicesAphena 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!---### **Why Join Aphena? – Our Benefits** **Employee Medical Premiums:** 75% paid by Aphena **Medical Deductible:** Partially covered by the company **Company-Paid Short-Term Disability & Life Insurance** **401(k) with Company Match** **PTO Accrual after 90 Days** **Paid Holidays & More!**---### **What You’ll Be Doing – Key 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**## Qualifications### **What You Need – Required Skills & Experience** **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**Preferred Skills:** Knowledge of **Statistical Process Control (SPC)** Ability to **flowchart and graph data**---### **What We’re Looking For – Personal Attributes** **Dependable, energetic, and self-motivated** **Works well under pressure and with minimal supervision** **Trustworthy and detail-oriented** **Flexible and able to prioritize tasks effectively**---### **Physical Requirements** Must be able to lift and move materials up to **50 lbs** Will be exposed to **dust, perfumes, and chemicals** Work includes **climbing, walking, stooping, kneeling, crouching, reaching, standing, pushing, pulling, lifting, grasping, twisting, and sitting** **Good visual awareness** required---### **Education & Experience** **High school diploma required** (advanced coursework preferred) **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---### **Ready to Make an Impact? Apply Today!**Join Aphena Pharma Solutions and be part of a team committed to **quality, safety, and excellence** in pharmaceutical manufacturing! #J-18808-Ljbffr