Process Validation

Immediate hiring for Process Validation / Automation Engineer – (Contract-to-Hire)

Location:

San Diego, CA (On-Site)

Contract: 6 Months (Contract-to-Hire)

Key Responsibilities

Develop and execute PPQ protocols for automated CGT manufacturing equipment

Support Computer Systems Validation (CSV) activities

Assist with MES implementation and validation

Ensure compliance with clinical manufacturing and regulatory requirements

Support Drug Substance, Drug Product, and Fill-Finish operations

Required Skills & Experience

Process validation of automated CGT manufacturing processes

Hands-on CSV experience and familiarity with MES systems

Strong understanding of clinical manufacturing regulations (GxP)

Experience in Drug Product / Drug Substance / Fill-Finish

Preferred Qualifications

7–15 years in Process Development, Validation, or Automation

Ability to work independently and manage multiple projects

Strong problem-solving and execution skills

Conversion Opportunity

Contract-to-hire: Strong performers may convert to full-time after 6 months

Seniority level

Not Applicable

Employment type

Full-time

Job function

Engineering

Industries

Pharmaceutical Manufacturing