CQV Engineer

Job Description:

Join our team as a CQV Engineer for a 2year project to support the expansion of a pharmaceutical facility in the Greater Los Angeles area. Starting in the 2nd week of July youll bring your 5 years of experience in Project Engineering and Validation to oversee Engineering and CQV activities.

Responsibilities:

• Support project engineering (specifications SOPs MOC risk/gap assessments)
• Collaborate on design (conceptual basic detailed)
• Manage safety and quality plans (JHA lockout/tagout permits)
• Oversee validation (IQ OQ PQ process validation software validation)
• Compile validation reports and documentation

Qualifications:

• Bachelors degree in Engineering Life Sciences or related field
• 5 years in FDAregulated industry
• Knowledge of cGMP and regulatory standards
• Proficiency in project engineering and construction activities
• Experience with pharmaceutical process equipment and instrumentation
• Strong problemsolving leadership and project management skills
• Proficiency in Microsoft Office and technical writing

Required Skills:

• Project Engineering
• Validation (Equipment Process Cleaning Facility Software)
• cGMP and regulatory compliance
• Risk and gap assessments
• Safety and quality management
• Technical writing and documentation
• Microsoft Office (Word Excel PowerPoint MS Project Visio)

Apply now to be a part of this exciting project!