Validation Engineer

GBA; Lenexa (KS); On-site; USD 81,000 - 135,000; Full time

Job summary

A leading company in the Life Sciences industry, GBA is seeking a Mid-Senior Level Validation Engineer to support projects across the Kansas City Metro area. The role involves delivering lifecycle documents and working on CQV activities, ideal for candidates with a scientific background and at least 3 years of experience. Join a team that values innovative solutions and promotes diversity in the workforce.

Qualifications

• Minimum 3 years experience specific to CQV activities.
• Strong problem-solving skills required.
• Experience in engineering, biology, microbiology, chemistry, etc. is preferred.

Responsibilities

• Support projects in the Kansas City Metro Area for Life Science industry clients.
• Develop various lifecycle documentation and validation documentation.
• Execute protocols and develop summary reports.

Skills

Interpersonal skills

Communication skills

Critical thinking

Education

BS in science related field

Job description

4 weeks ago Be among the first 25 applicants

Compli, LLC was founded in 2001 to provide Commissioning, Validation and Regulatory Support Services to the Life Sciences industry.

We serve pharmaceutical companies across the United States, offering a vast array of services that assist companies with exceeding their goals and objectives. In today’s world, it’s never been more important to understand regulations and quality assurance activities as they relate to operations, vendors, engineering, construction and contractors. In 2020, Compli, LLC became a wholly owned subsidiary of George Butler Associates, Inc. This acquisition allowed Compli, LLC to become part of an integrated network of services where clients have more options to engage an impressive suite of in-house services.

Essential Functions

• Support Projects in greater Kansas City Metro Area for Life Science Industry clients.
• Efforts consist of providing project deliverables to clients around Life cycle validation efforts.
• This included, but is not limited to, developing Life cycle documentation (URS’s, Trace Matrices, System/Component Impact Assessments, Risk Assessments, Master Planning, etc.), developing Commissioning, Qualification and Validation documentation (CQV protocols, executing protocols, developing summary reports and final report packages).
• Other duties as assigned.
  
  

Education & Experience

• BS in science related field (e.g., engineering, biology, microbiology, chemistry, etc.).
• Minimum 3 years experience specific to CQV activities.
• Must have strong interpersonal and communication skills.
• Must have strong critical thinking skills.
  
  

Travel

• Working in Lenexa, KS metro area.
• Willing to travel to project sites across the US is a plus but not required.
  
  

It's more than just a job...

At Compli, we are about innovative and intelligent people who want to solve problems. We’re known for our technical excellence, but we bring so much more to the table. We strive to create remarkable solutions for a higher quality of life. And we are changing the industry by integrating the design and construction process with use of new technology.

At Compli, we are an Equal Employment Opportunity Employer promoting diversity in our workforce by including all individuals regardless of age, race, religion, color, sex, national origin, marital status, genetic information, sexual orientation, gender identity, gender expression, disability, veteran status, pregnancy status, or any other status protected by law.

Seniority level

• Seniority level

  Mid-Senior level

Employment type

• Employment type

  Full-time

Job function

• Job function

  Strategy/Planning and Information Technology

• Industries

  Design Services

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