GMP Packaging Technician II - 1st Shift

System One

Macungie (Lehigh County)

On-site

USD 22,000 - 30,000

Full time

14 days+
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Job summary

System One is seeking a Packaging Associate II for 1st shift in Macungie, PA. This contract-to-hire role pays $19.00 per hour and runs 7:00 AM to 3:00 PM, Monday through Friday, within a pharmaceutical manufacturing setting.

Responsibilities include GMP compliance, quality inspections, and documentation verification, ensuring finished goods meet batch records. Candidates should have a high school diploma and prior GMP experience.

Qualifications

  • High School diploma or equivalent.
  • Experience with GMP quality or manufacturing in a regulated environment, including visual inspections and document verification.
  • Knowledge of cGMP (21CFR 210, 211, 820) and/or DEA regulations for controlled substances.
  • Ability to perform quality inspections and support GMP compliance.
  • Strong attention to detail and documentation skills.

Responsibilities

  • Adhere to and enforce GMP compliance, perform quality inspections related to contract packaging, including equipment challenges and verification, components, bulk product, work-in-process, and finished goods
  • Read and understand process steps within the packaging record to ensure compliance during the packaging process
  • Assist with overall efficiency of the production within the assigned rooms
  • Inspect units for quality as they are packaged, performing visual, functional, destructive, and count checks as required per packaging record and AQL requirements
  • Verify the accuracy, completeness, and supported documentation of the packaging requirements outlined in the Batch Record and ensure all are supported by appropriate documentation

Skills

Attention to detail
Documentation skills
GMP compliance understanding

Education

High School diploma or equivalent

Job description

System One is seeking a Packaging Associate II for 1st shift in Macungie, PA. This contract-to-hire role pays $19.00 per hour and runs 7:00 AM to 3:00 PM, Monday through Friday, within a pharmaceutical manufacturing setting.

Responsibilities include GMP compliance, quality inspections, and documentation verification, ensuring finished goods meet batch records. Candidates should have a high school diploma and prior GMP experience.

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