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60 3 Key Consulting Automation Engineer Jobs Hiring Near You

ettain group

Automation Developer/Engineer

Dallas, TX · On-site

... Engineer Key Words Java, JBehave or Cucumber, Groovy, Selenium WebDriver, PhantomJS, Jenkins ... Whether you are looking for a technology consulting project or a full-time IT job, ettain group can ...

ettain group

Automation Developer/Engineer

Dallas, TX

... Engineer Key Words Java, JBehave or Cucumber, Groovy, Selenium WebDriver, PhantomJS, Jenkins ... Whether you are looking for a technology consulting project or a full-time IT job, ettain group can ...

S R International, Inc.

Automation Engineer

Key Responsibilities * Design, build, test, and deploy end-to-end RPA workflows using UiPath ... About SR International INC SR International has been a leading name among the IT consulting ...

Slater Consult

Automation Engineer

Raleigh, NC · On-site

Key Responsibilities * Provide on-site automation engineering support and troubleshooting * Design ... Strong problem-solving skills and ability to work in a consultative role About Confirm Automation ...

AccuScan Sciences

Automation Engineer III

Milpitas, CA · On-site

As an Automation Engineer III at AccuScan Sciences you will assume a strategic role, responsible ... KEY RESPONSIBILITES * Leads strategic planning and execution of automated processes, working ...

AccuScan Sciences

Automation Engineer III

Milpitas, CA · On-site

As an Automation Engineer III at AccuScan Sciences you will assume a strategic role, responsible ... KEY RESPONSIBILITES * Leads strategic planning and execution of automated processes, working ...

Faithtechnologies

Automation Engineer III

Menasha, WI · On-site

The Automation Engineer III is responsible for the software design and implementation, and support ... KEY RESPONSIBILITIES * Methodically approaches the process startup. * Demonstrates strong ...

CapTech Consulting

Test Automation Engineer

Richmond, VA · On-site

$45.50 - $60/hr

Key Responsibilities * Design, develop, and maintain automated functional, regression, and ... Three to six years of professional experience in software quality engineering, with at least two ...

CapTech Consulting

Test Automation Engineer

Richmond, VA · On-site

$45.50 - $60/hr

Key Responsibilities * Design, develop, and maintain automated functional, regression, and ... Three to six years of professional experience in software quality engineering, with at least two ...

CapTech Consulting

Test Automation Engineer

Richmond, VA · On-site

$45.50 - $60/hr

Key Responsibilities * Design, develop, and maintain automated functional, regression, and ... Three to six years of professional experience in software quality engineering, with at least two ...

CapTech Consulting

Test Automation Engineer

Richmond, VA · On-site

$45.50 - $60/hr

Key Responsibilities * Design, develop, and maintain automated functional, regression, and ... Three to six years of professional experience in software quality engineering, with at least two ...

CapTech Consulting

Test Automation Engineer

Richmond, VA · On-site

$45.50 - $60/hr

Key Responsibilities * Design, develop, and maintain automated functional, regression, and ... Three to six years of professional experience in software quality engineering, with at least two ...

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Senior CQV Engineer - GMP Equipment, Utilities & Facilities Qualification - (JP15486)

3 Key Consulting

Thousand Oaks, CA • Hybrid

$66 - $72/hr

Full-time

Re-posted 17 days ago

Job description

Job Title: Senior CQV Engineer – GMP Equipment, Utilities & Facilities Qualification - (JP15486)
Location: Thousand Oaks, CA. 91320 (Hybrid)
Employment Type: Contract
Business Unit: Engineering Systems
Duration: 1+ year (with likely extensions and/or conversion to permanent)
Posting Date: 06/16/26
Pay Rate: $66 - $72/hour W2
Notes: Only qualified candidates need apply. Local, onsite at least 3 days weekly 8-5
3 Key Consulting is hiring a Senior CQV Engineer – GMP Equipment, Utilities & Facilities Qualification  for a consulting engagement with our direct client, a leading global biopharmaceutical company.
Job Description:
Primarily responsible for leading and/or executing commissioning and qualification activities on new or modified GMP analytical and process equipment, utilities, and facilities. Responsibilities include generating/reviewing/executing C&Q protocols, plans, and summary reports. Works with project teams and SMEs to develop testing strategies. Participates in project meetings to inform stakeholders on progress of C&Q activities.
Why is the Position Open?
Planned Project.
Top Must Have Skills:
  • Experience in commissioning/qualification/validation
  • Experience in a GMP environment

Day to Day Responsibilities:
  • Plan and track implementation of commissioning & qualification actions/documentation versus project(s) timelines.
  • Work with project teams to develop the commissioning and qualification strategy and document in qualification plans.
  • Generate/evaluate qualification/validation protocols including IQ, OQ, FT, PQ protocols and final reports for new or modified GMP analytical and process equipment, utilities, and facilities.
  • Execute IQ, OQ, FT, PQ protocols, which may involve protocol discrepancies, investigation, and corrective action activities for new or modified GMP analytical and process equipment, utilities, and facilities.
  • Ensure that Qualification/Validation plans are generated and updated for all ongoing projects.
  • Prepare, evaluate and approve technical and GMP linked documentation such as URS, FMEA, impact/risk assessment, master plans, qualification/validation documentation.
  • Develop and/or execute FAT/SAT and other commissioning activities for new GMP systems in collaboration with both internal and external partners.
  • May include conducting validation maintenance activities including performing and scheduling periodic reviews.
  • Other duties may be assigned to this role.

Basic Qualifications:
Doctorate degree OR Masters degree and 2 years of experience OR Bachelors degree and 4 years of experience OR Associates degree and 8 years of experience OR High school diploma / GED and 10 years of experience
 
  • Demonstrable experience in a pharmaceutical, biotech, or life science organization in a C&Q/CQV role.
  • Knowledge of cGMP commissioning/qualification/validation practices.
  • Familiarity with Kneat Gx Platform or other digital C&Q systems.
  • Experience working with cross-functional stakeholders.
  • Knowledge of quality assurance principles.
  • Experience working within project teams and multiple projects in parallel.
  • Effective communication skills, both verbal and written.
  • Able to think analytically with the ability to resolve issues.
  • Able to manage own time efficiently.

Red Flags:
Short tenures at previous jobs (?2 years), not local and not willing to relocate
Interview process:
1-2 Stages of interview | Video interview (Teams)
We invite qualified candidates to send your resume to resumes@3keyconsulting.com.  If you decide that you’re not interested in pursuing this particular position, please feel free to take a look at the other positions on our website www.3keyconsulting.com/careers. You are also welcome to share this opportunity with anyone you think might be interested in applying for this role.