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Quality Technician

Aphena Pharma Solutions Β· Liquid and Topicals Division MD - Easton, MD 21601

Other EngineeringExternal listingfull-timeabout 1 month ago

About The Role

Description

Now Hiring: Experienced Quality Technician – Day Shift

πŸ“ Location: Easton, Maryland

πŸ•’ Schedule: Monday – Thursday | 4 x 10-hour shifts (6:30 AM – 5:30 PM)

πŸ‘¨β€βš•οΈ Industry: Pharmaceutical, OTC, Dietary Supplements, & 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

βœ” Medical, Dental, Vision Coverage - BC/BS - large In-Network Directory

βœ” Medical Deductible: Partially covered by the company (HRA); HSA

βœ” Company-Paid Life Insurance

βœ” 401(k) with Company Match

βœ” PTO Accrual after 90 Days

βœ” Paid Holidays

What You’ll Be Doing – Key Responsibilities

πŸ”Ή Inspect incoming components, in-process products, and finished products based on specifications

πŸ”Ή Review documentation before production starts and perform First Piece Approval (FPA)

πŸ”Ή Record and maintain data following Good Documentation Practices (GMP)

πŸ”Ή Prepare inspection sheets & forms using Microsoft Word and Excel

πŸ”Ή Troubleshoot quality concerns on the production floor

πŸ”Ή Review & verify accuracy of all paperwork, including Device/Drug History Records (DHR)

πŸ”Ή Ensure calibration of all inspection/test equipment and maintain accurate records

πŸ”Ή Investigate and gather data for customer complaints

πŸ”Ή Assist in process validations and maintain compliance with ISO & FDA GMP regulations

πŸ”Ή Perform data entry and retrieval using Aphena’s computer system

πŸ”Ή Support CAPA processes (Corrective & Preventive Action Plans)

πŸ”Ή Document and resolve non-conforming materials and process discrepancies

πŸ”Ή Generate controlled labels and handle approvals/documentation

πŸ”Ή Maintain a clean and organized work area

Qualifications

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

Preferred Skills

  • βž• Knowledge of Statistical Process Control (SPC)
  • βž• Ability to flowchart and graph data
  • What We’re Looking For – Personal Attributes
  • βœ” Dependable, energetic, and self-motivated
  • βœ” Works well under pressure and with minimal supervision
  • βœ” Trustworthy and detail-oriented
  • βœ” Flexible and able to prioritize tasks effectively

Physical Requirements

  • πŸ›  **Must be able to lift and move materials up to 50 lbs
  • πŸ›  Will be exposed to dust, perfumes, and chemicals
  • πŸ›  Work includes climbing, walking, stooping, kneeling, crouching, reaching, standing, pushing, pulling, lifting, grasping, twisting, and sitting
  • πŸ›  Good visual awareness required**

Education & Experience

  • πŸŽ“ High school diploma required (advanced coursework preferred)
  • πŸ“œ Previous experience with GMP regulations in pharmaceuticals or medical devices
  • πŸ’» 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! πŸš€

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