GMP Manufacturing Associate II: Parenteral Packaging

Randstad USA

Norwood (MA)

On-site

USD 41,000 - 45,000

Full time

2 days ago
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Job summary

Randstad USA in Norwood, MA is seeking an experienced Manufacturing Associate II to support cGMP labeling and packaging for parenteral drug products. This 100% onsite role requires precise operation, adherence to ALCOA+ documentation, and a strong eye for detail.

You will execute line setup, labeling, cartoning, kitting, and case packing; perform line clearances and material staging; maintain label control and perform in-process checks, including barcode verifications.

Qualifications

  • High School Diploma or GED required; science/tech degree preferred.
  • 1–3 years of GMP manufacturing or regulated operations experience.
  • Experience with batch records and label reconciliation.
  • Ability to stand for long periods and lift up to 35 lbs.
  • Flexibility for off-hours and overtime to support production demands.

Responsibilities

  • Execute line setup, operation, and changeover for labeling, cartoning, kitting, and case packing.
  • Perform room/equipment checks, line clearances, and material staging.
  • Support label issuance, reconciliation, and documentation accuracy.
  • Conduct in-process quality checks and barcode verifications.
  • Complete contemporaneous batch records and electronic logbooks (ALCOA+).
  • Collaborate with QA/QC, MS&T, Engineering, and Supply Chain to drive improvements.

Skills

GMP manufacturing
ALCOA+
5S housekeeping
Communication

Education

High School Diploma / GED
Associate’s or Bachelor's degree preferred

Tools

MES/eBR systems
Labeling systems
Electronic logbooks

Job description

Randstad USA in Norwood, MA is seeking an experienced Manufacturing Associate II to support cGMP labeling and packaging for parenteral drug products. This 100% onsite role requires precise operation, adherence to ALCOA+ documentation, and a strong eye for detail.

You will execute line setup, labeling, cartoning, kitting, and case packing; perform line clearances and material staging; maintain label control and perform in-process checks, including barcode verifications.

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