Pharma Quality Technician – GMP/ISO (Day Shift)

Aphena Pharma Solutions, Inc.; Easton (MD); On-site; USD 24,796 - 30,307; Full time

Benefits offered by this job

Medical premiums paid 75%

401(k) with company match

PTO accrual after 90 days

Paid holidays

Job summary

Aphena Pharma Solutions, Inc. in Easton, MD is seeking an Experienced Quality Technician for the day shift to inspect incoming components, in‑process products and finished goods, ensuring GMP and ISO compliance.

You will review documentation before production starts, perform First Piece Approval (FPA), maintain calibration records, assist in CAPA activities and support data entry in Word and Excel. Strong attention to detail, problem solving, and clear communication with vendors and

Qualifications

• High school diploma required; advanced coursework preferred.
• GMP experience in pharmaceuticals or medical devices.
• Proficient in Microsoft Word and Excel.
• Strong problem-solving and troubleshooting abilities.
• Detail-oriented with excellent communication and organization.
• Ability to read and interpret drawings and technical documentation.
• Experience in Quality Control preferred.

Responsibilities

• Inspect incoming components, in-process products, and finished goods.
• Review documentation before production starts and perform First Piece Approval (FPA).
• Record and maintain data per GMP.
• Prepare inspection sheets using Word/Excel.
• Troubleshoot quality concerns on the production floor.
• Verify Device/Drug History Records (DHR) and calibration of equipment.
• Support CAPA processes and ISO/FDA GMP compliance.
• Maintain a clean and organized work area.

Skills

MS Word & Excel

GMP & ISO Knowledge

Organizational skills

Communication skills

Detail-oriented

Reading drawings & technical docs

Quality Control experience

Education

High school diploma

Tools

SPC

Job description

Aphena Pharma Solutions, Inc. in Easton, MD is seeking an Experienced Quality Technician for the day shift to inspect incoming components, in‑process products and finished goods, ensuring GMP and ISO compliance.

You will review documentation before production starts, perform First Piece Approval (FPA), maintain calibration records, assist in CAPA activities and support data entry in Word and Excel. Strong attention to detail, problem solving, and clear communication with vendors and