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Quality Technician

Job in Easton, Talbot County, Maryland, 21601, USA
Listing for: Aphena Pharma Solutions
Full Time position
Listed on 2026-07-11
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Quality Control - QC Analysts/Managers
Job Description & How to Apply Below

Quality Technician

Liquid and Topicals Division MD - Easton, MD 21601

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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