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Quality Technician

Aphena Pharma Solutions
Posted 15 days ago, valid for 9 days
Location

Easton, MD 21601, US

Salary

$18 - $22 per hour

Contract type

Full Time

Paid Time Off
Life Insurance

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Sonic Summary

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  • Aphena Pharma Solutions is seeking an Experienced Quality Technician for their Liquid and Topicals Division in Easton, MD, offering a salary range of $18.00 - $22.00 hourly.
  • The position requires a high school diploma and previous experience with GMP regulations in pharmaceuticals or medical devices.
  • Key responsibilities include inspecting products, reviewing documentation, and ensuring compliance with ISO and FDA GMP regulations.
  • Candidates should possess strong organizational skills, proficiency in Microsoft Word and Excel, and excellent communication abilities.
  • The work schedule is Monday to Thursday with potential mandatory overtime on Fridays, and no travel is required.

Job DetailsLevel: ExperiencedJob Location: Liquid and Topicals Division MD - Easton, MD 21601Position Type: Full TimeEducation Level: High SchoolSalary Range: $18.00 - $22.00 HourlyTravel Percentage: NoneJob Shift: AnyJob Category: QA - Quality ControlNow Hiring: Experienced Quality Technician – Day Shift Location: Easton, Maryland Schedule: Monday – Thursday | 4 x 10-hour shifts (6:30 AM – 5:30 PM) 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 HolidaysΒ  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 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 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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