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Validation Engineer

Contract: Carlsbad, California, US

Salary Range: 30.00 - 40.00 | Per Hour

Job Code: 371407

End Date: 2026-09-30

Days Left: 13 days, 8 hours left

Job Summary:
The Validation Engineer II will support validation activities for GMP manufacturing facilities, utilities, equipment, laboratory systems, and processes within a regulated environment. The role is responsible for developing validation strategies, authoring lifecycle documentation, executing qualification protocols, and maintaining compliance with quality and regulatory requirements. This position works closely with cross-functional teams to ensure systems and processes remain in a validated state throughout their lifecycle.

Key Responsibilities:

  • Develop and execute validation strategies for GMP facilities, utilities, process equipment, laboratory systems, and analytical instruments
  • Author and execute Validation Master Plans, qualification plans, and validation protocols using risk-based methodologies
  • Develop and review User Requirements Specifications, functional requirements, risk assessments, and Requirements Traceability Matrices
  • Create and execute Installation Qualification, Operational Qualification, and Performance Qualification protocols
  • Lead or support process validation, engineering studies, test method validation, and equipment qualification activities
  • Manage validation protocol execution to ensure timely completion and compliance with regulatory requirements
  • Evaluate validation results, investigate deviations, and prepare validation reports and corrective action documentation
  • Support commissioning, installation verification, startup activities, and transfer of systems into GMP operations
  • Review change control documentation and assess validation impact for process, equipment, and system changes
  • Track validation project progress and provide status updates to stakeholders
  • Collaborate with equipment vendors and internal teams during qualification and commissioning activities
  • Participate in internal and external audits and present validation status and recommendations during project reviews
  • Provide technical guidance and mentorship to less experienced team members

    Required Qualifications:
  • Bachelor’s Degree in Engineering, Life Sciences, Biotechnology, Quality, or a related field
  • Minimum 2 years of experience in validation, qualification, engineering, or quality within a regulated environment
  • Experience developing and executing validation lifecycle documentation including Validation Master Plans, User Requirements Specifications, risk assessments, and Requirements Traceability Matrices
  • Experience executing Installation Qualification, Operational Qualification, and Performance Qualification activities
  • Knowledge of GMP regulations, quality systems, and validation principles
  • Experience supporting change control, deviation investigations, and corrective action activities
  • Strong technical writing, analytical, and problem-solving skills
  • Ability to work effectively within cross-functional teams and manage multiple priorities

Preferred Qualifications:

  • Master’s Degree in a related field
  • Experience validating GMP manufacturing equipment used in biotechnology, biologics, pharmaceutical, or oligonucleotide manufacturing environments
  • Hands-on experience with analytical instrumentation including HPLC systems, chromatography data systems, and spectrophotometers
  • Experience with automated purification systems, tangential flow filtration, and chromatography platforms
  • Knowledge of commissioning and qualification activities for manufacturing facilities, cleanrooms, laboratories, and utilities
  • Experience collaborating with equipment vendors and reviewing vendor qualification documentation
  • Experience supporting full validation lifecycle activities from commissioning through ongoing validated-state maintenance

Benefits:

The Company offers the following benefits for this position, subject to applicable eligibility requirements: medical insurance, dental insurance, vision insurance, 401(k) retirement plan, life insurance, long-term disability insurance, short-term disability insurance, paid parking/public transportation, paid time off, paid sick and safe time, hours of paid vacation time, weeks of paid parental leave, and paid holidays annually – as applicable.

Pay Range: $30/hr to $40/hr

 

 

Job Requirement
  • GMP
  • IQ/OQ/PQ
  • Validation
  • Commissioning
  • Qualification
  • Process Validation
  • Risk Assessment
  • Change Control
  • HPLC
  • Laboratory Systems
  • Biotechnology Manufacturing
  • Technical Documentation
Reach Out to a Recruiter
  • Recruiter
  • Email
  • Phone
  • Gagandeep Singh
  • gagandeep.singh@collabera.com
  • 7042475816
Apply Now
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