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Open nowPosted 2 days ago

Quality Assurance Specialist - Drug Product

BioPharma Consulting JAD Group

Where
Juncos, Puerto Rico
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Your applicationOpen nowQuality Assurance Specialist - Drug ProductBioPharma Consulting JAD Group · Juncos, Puerto Rico

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  2. CV RocketCV written for this posting.

  3. 25 readersRecruiter, hiring manager, skeptic. Round after round.

  4. CV RocketApplied on BioPharma Consulting JAD Group's own form.

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The clock on this job

Early applications get read.

12.3% of postings close within 7 days. Measured by our own scanner across the market.

Share of postings closed within
  1. 2.1%1 day
  2. 4.5%3 days
  3. 12.3%7 days
  4. 19.3%14 days
  5. 35.6%30 days
  6. 58.1%60 days
This job: posted 2 days ago

The posting

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
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