Senior Validation Engineer

Thousand Oaks, CA, US • Posted 60+ days ago • Updated 9 hours ago
Full Time
On-site
Fitment

Dice Job Match Score™

✨ Finding the perfect fit...

Job Details

Skills

  • Regulatory Compliance
  • Editing
  • Collaboration
  • Manufacturing
  • Quality Control
  • Quality Assurance
  • Leadership
  • Management
  • Root Cause Analysis
  • Life Sciences
  • Pharmaceutics
  • Computerized System Validation
  • Good Manufacturing Practice
  • GAMP
  • Documentation
  • Analytical Skill
  • Conflict Resolution
  • Problem Solving

Summary

Job Description:
This position is responsible for planning, executing, and documenting commissioning, qualification, and validation (CQV) activities to ensure all systems meet stringent regulatory and client-specific requirements.
The Senior Validation Engineer will act as a subject matter expert, collaborating closely with cross-functional teams, including Manufacturing, Facilities, Quality Control and Quality Assurance to deliver robust validation strategies that enable compliant and efficient operations in an early-phase clinical environment.

Roles & Responsibilities:
Independently understanding quality standards, cGMP's, and regulatory standards to support team in compliance of validation effort.
Authoring, editing, and executing technical commissioning, qualification and validation documentation for facilities, utilities, and standard equipment/systems/software.
Actively consult clients on regulatory validation processes and standard industry acceptable practices.
Collaborate with cross-functional teams including Manufacturing, Facilities, Quality Control nd Quality Assurance to ensure validation activities are properly scoped and executed.
Ability to take independent leadership role on project(s).
Managing and working collaboratively with clients' quality representative to complete deviation investigation and resolution for problems and issues encountered during execution ctivities. Includes ability to complete root cause analysis.

Education & Experience:
Bachelor's degree in engineering, Life Sciences, or a related field.
5+ years of relevant experience in validation within a regulated industry (e.g., pharma, biotech).
Experience with facility, utility, equipment, and computer system validation. Preferably in start-up of early-phase clinical biomanufacturing facilities.
Strong knowledge of validation principles, cGMP, FDA regulations (21 CFR Part 11, Part 210/211), and industry guidelines (e.g., ISPE, GAMP).
Experience working with start-up clients, without well established company procedures nd standards.
Excellent documentation, analytical, and problem-solving skills.
Ability to work independently and as part of a team
Employers have access to artificial intelligence language tools (“AI”) that help generate and enhance job descriptions and AI may have been used to create this description. The position description has been reviewed for accuracy and Dice believes it to correctly reflect the job opportunity.
  • Dice Id: 91116760
  • Position Id: f34301439d1553c0a13a70666335ae3
  • Posted 30+ days ago
Create job alert
Set job alertNever miss an opportunity! Create an alert based on the job you applied for.

Similar Jobs

Torrance, California

Today

Full-time

USD 98,500.00 - 123,100.00 per year

San Diego, California

Today

Easy Apply

Full-time

USD 65.00 - 75.00 per hour

Thousand Oaks, California

Today

Full-time

Santa Clara, California

Today

Full-time

USD 121,400.00 - 181,800.00 per year

Search all similar jobs