Quality Technician
Job in
Easton, Talbot County, Maryland, 21601, USA
Listed on 2026-07-17
Listing for:
Aphena Pharma Solutions, Inc.
Full Time
position Listed on 2026-07-17
Job specializations:
-
Quality Assurance - QA/QC
Quality Control - QC Analysts/Managers, Quality Engineering, Production QC/QA
Job Description & How to Apply Below
- Easton, MD 21601## Overview Salary Range $18.00 - $22.00 Hourly Level Experienced Position Type Full Time Job Shift Any Education Level High School
Travel Percentage None Category QA
- 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 Devices 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!---###
** 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!
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