# Quality Assurance Specialist - Drug Product

> BioPharma Consulting JAD Group · Juncos, Puerto Rico · Contract · Posted 2026-10-24

**Workplace:** on_site

**Department:** Amgen

## Description

Provide Quality oversight of drug product manufacturing, packaging and inspection operations at a leading biotechnology company in Juncos, Puerto Rico. You will work with minimal supervision and make the quality calls that keep product moving.

**What you'll do**

-   Review and approve master production records, process validation protocols and reports.
-   Approve change controls, nonconformances, investigations and CAPA records.
-   Represent Quality on incident triage and new product introduction teams.
-   Review risk assessments, work orders and EMS/BMS alarms.
-   Provide lot disposition and authorize lots for shipment.

## Requirements

-   Bachelor's degree + 4 years (or Master's + 2, Associate's + 8, or High School + 10) of directly related experience.
-   GMP Quality Assurance experience approving change controls, deviations, CAPAs, protocols and procedures.
-   Packaging and/or inspection operations experience preferred.
-   Good Documentation Practices and electronic quality systems.
-   Bilingual English/Spanish.

## Benefits

-   Contract: 5 months, with possible extension
-   Shift: Administrative, Monday–Friday (40 hours/week)
-   Start: Immediate

## Apply

[Apply at BioPharma Consulting JAD Group](https://apply.workable.com/biopharma-consulting-jad-group/j/40336C0278/apply)

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