MES/PAS-X Engineer: Electronic Batch Records in Biopharma

3key Consulting, Inc.

Thousand Oaks (CA)

On-site

USD 177,655,000 - 191,982,000

Part time

3 days ago
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Job summary

3 Key Consulting is hiring an MES / PAS-X Engineer to support a leading global biopharmaceutical company in Thousand Oaks, CA. The role focuses on electronic batch records, MES functionality, and NPI/EBR metrics, collaborating with GMP operations and process development teams.

You will generate electronic documentation, validate EBRs, and contribute to continuous improvement and the plant's digital transformation.

Qualifications

  • Doctorate degree or Masters with 2+ years, or Bachelor’s with 4+ years, or Associate’s with 8+ years, or HS diploma with 10+ years.
  • Experience with PAS-X EBR in a GMP environment.
  • Knowledge of PAS-X integration with SAP, PI, DeltaV, and Rockwell.
  • Strong operations knowledge of drug product manufacturing.
  • Ability to work in a distributed team and manage project deliverables.

Responsibilities

  • Manufacture Electronic Batch Records (EBR) using PAS-X.
  • Validate new Electronic Batch Records (ALM).
  • Assist in implementing new MES functionality (EQM, PCS MBR Elements).
  • Develop standard work and processes for MES features.
  • Contribute to Lean transformation via NPI/EBR metrics and CI tools.
  • Participate in projects to introduce new products and manufacturing tech.
  • Engage with client network to align EBR differences and path forward.

Skills

MES PAS-X experience
Attention to detail
Continuous improvement mindset

Education

Doctorate degree
Master’s degree
Bachelor’s degree
Associates degree
High school diploma

Tools

PAS-X (Korber)
SAP
PI
DeltaV
Rockwell

Job description

3 Key Consulting is hiring an MES / PAS-X Engineer to support a leading global biopharmaceutical company in Thousand Oaks, CA. The role focuses on electronic batch records, MES functionality, and NPI/EBR metrics, collaborating with GMP operations and process development teams.

You will generate electronic documentation, validate EBRs, and contribute to continuous improvement and the plant's digital transformation.

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