Deviations & Investigations Owner – GMP Biopharma

BioPharma Consulting JAD Group

Juncos (PR)

On-site

USD 60,000 - 90,000

Full time

3 days ago
Be an early applicant

A complete application in a minute

Tailored resume and cover letter, ready to send.

Get past ATS filters

Job summary

BioPharma Consulting JAD Group is seeking a candidate to own deviations from triage to closure in a drug substance operation in Juncos, Puerto Rico. The role requires leading investigations and delivering timely closure with strong RCA skills.

Responsibilities include revising procedures, supporting process monitoring, change controls, and new product introductions. Bilingual English/Spanish is required, with shift Monday–Friday, 8:00 am–5:00 pm, start immediately.

Qualifications

  • Bachelor's degree + 4 years (or Associate's + 8, or High School + 10) in manufacturing operations.
  • Deviation/investigation owner experience in GMP manufacturing (required).
  • Bioprocessing unit operations, Lean, GDP.
  • TrackWise, Veeva, MES, CDOCS; Smartsheet and Power BI are a plus.

Responsibilities

  • Own nonconformances: triage, investigation, root cause, CAPA and on-time closure.
  • Use RCA tools (Fishbone, 5 Whys, Kepner-Tregoe) and write clear investigation reports.
  • Revise manufacturing procedures and support process monitoring.
  • Support change controls and new product introductions.

Skills

Root cause analysis
Investigation leadership
GMP manufacturing
Bilingual English/Spanish

Education

Bachelor's degree in manufacturing operations
Associate's degree in manufacturing operations
High School diploma

Tools

TrackWise
Veeva
MES
CDOCS
Smartsheet
Power BI

Job description

BioPharma Consulting JAD Group is seeking a candidate to own deviations from triage to closure in a drug substance operation in Juncos, Puerto Rico. The role requires leading investigations and delivering timely closure with strong RCA skills.

Responsibilities include revising procedures, supporting process monitoring, change controls, and new product introductions. Bilingual English/Spanish is required, with shift Monday–Friday, 8:00 am–5:00 pm, start immediately.

Get your free, confidential resume review.

or drag and drop your file here.

Similar jobs

Similar jobs worth comparing

Lead Biotech Manufacturing Deviations & Investigations
Lead Biotech Manufacturing Deviations & Investigations

Biopharma-Consulting-Jad-Group • Juncos (PR)

On-site
USD 55,000 - 83,000
Manufacturing Specialist - Deviations and Investigations
Manufacturing Specialist - Deviations and Investigations

Biopharma-Consulting-Jad-Group • Juncos (PR)

On-site
USD 55,000 - 83,000
Manufacturing Specialist - Deviations and Investigations
Manufacturing Specialist - Deviations and Investigations

BioPharma Consulting JAD Group • Juncos (PR)

On-site
USD 60,000 - 90,000
Biotech QA Specialist - GMP, CAPA & Change Control
Biotech QA Specialist - GMP, CAPA & Change Control

Biopharma-Consulting-Jad-Group • Juncos (PR)

On-site
USD 45,000 - 67,000
GMP QA Specialist: Drug Manufacturing & Release
GMP QA Specialist: Drug Manufacturing & Release

BioPharma Consulting JAD Group • Juncos (PR)

On-site
USD 39,000 - 52,000
Bioprocess Inspection Specialist - Vials & Packaging
Bioprocess Inspection Specialist - Vials & Packaging

Biopharma-Consulting-Jad-Group • Juncos (PR)

On-site
USD 90,000 - 130,000
On-the-Floor GMP Troubleshooting Engineer
On-the-Floor GMP Troubleshooting Engineer

Biopharma-Consulting-Jad-Group • Juncos (PR)

On-site
USD 84,000 - 123,000
QA Specialist - cGMP Biopharma | On-Site PR
QA Specialist - cGMP Biopharma | On-Site PR

Biopharma-Consulting-Jad-Group • Juncos (PR)

On-site
USD 60,000 - 90,000
Quality Assurance Specialist - Drug Product
Quality Assurance Specialist - Drug Product

Biopharma-Consulting-Jad-Group • Juncos (PR)

On-site
USD 45,000 - 67,000
Contract PM for Biopharma Manufacturing Ops (Onsite PR)
Contract PM for Biopharma Manufacturing Ops (Onsite PR)

BioPharma Consulting JAD Group • Juncos (PR)

On-site
USD 85,000 - 130,000