Think the best job opportunities are far away? Think again. Great opportunities are right here in your backyard.
Kelly® Engineering is looking for a Validation Specialist (Pack Engineering Support) to work at a premier manufacturing client in Añasco, PR.
Let us help you grow at work and discover the next step in your career, all while being a vital part of your community.

Compensation : From $25 by hr and up, based on experience
Shift                  : Admin, Monday through Friday. Available weekends, alternate shifts, after-hours activities when needed
Location           : On Site | Añasco, Puerto Rico

This job might be an outstanding fit if you have the following qualifications:

• Bachelor’s Degree in Engineering or a related technical discipline (required).
  

• Internship, co-op, or academic project experience within medical devices, manufacturing, quality, or packaging is considered as experience
  

• Experience working in a regulated industry (Medical Device, Pharmaceutical, Biotechnology, etc.).Experience with tray-sealing processes (required).
  

• Available for working in ISO Class 7 cleanroom environments and following strict gowning requirements.
  

• Demonstrate strong documentation, organizational, and communication skills.
  

• Fluent in English (read, write, speak, and understand).
  

• Proficient in Microsoft Office (Excel, Word, PowerPoint).
  

• Thrive in a fast-paced, collaborative manufacturing environment with a strong willingness to learn.
  

  • Preferred Requirements
    

    • At least 4+ years of engineering or manufacturing experience.
      

    • Experience with packaging validation, laboratory testing, or engineering projects.
      

    • Knowledge of FDA QSR, ISO 13485, ISO 9001, GMP, and medical device regulations.
      

    • Exposure to sterile barrier systems and validation methodologies.
      

    
    

What’s a typical day as Validation Specialist (Pack Engineering Support)? You’ll be:

• Supporting packaging validation and testing activities for sterile and non-sterile medical device packaging systems.
  

• Executing validation protocols, engineering studies, and testing activities in close collaboration with Packaging and Project Engineers.
  

• Collecting, analyzing, and documenting testing data and validation results.
  

• Preparing and maintaining technical documentation, including protocols, reports, and test summaries.
  

• Coordinating with cross-functional teams such as Quality, Operations, Regulatory, and Engineering.
  

• Supporting troubleshooting, risk assessments, process improvements, and packaging line trials.
  

• Ensuring compliance with internal procedures and applicable regulatory requirements.

Why you should apply to be Validation Specialist (Pack Engineering Support):

• Opportunity to work in a regulated medical device manufacturing environment.
  

• Competitive pay rate with room to grow based on experience.
  

• Collaborate with engineering, quality, and regulatory professionals on impactful validation projects.
  

• Work for a respected industry leader focused on safety, compliance, and continuous improvement.
  

• Gain valuable hands-on experience in packaging validation and technical documentation.
  

• Access to the following benefits:
  

  • Weekly pay (W2)
    

  • Sick, Vacations & Holidays paid*
    

  • Christmas bonus*
    

    • * Must comply with minimum established requirements to qualify.
      

    
    

What happens next

Once you apply, you’ll proceed to next steps if your skills and experience look like a good fit. But don’t worry—even if this position doesn’t work out, you’re still in our network. That means all of our recruiters will have access to your profile, expanding your opportunities even more.

Helping you discover what’s next in your career is what we’re all about, so let’s get to work.
Apply to be Validation Specialist (Pack Engineering Support) today!
Recruiter: Lilly Abouomar 9395454792
#SETTPR #KellyEngineering #Engineer #AnascoPR

10304633