Validation Engineer

Design Group

East Brunswick, NJ, United States
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Validation and fda compliance
Fat, sat, iq, oq documentation
Qms procedures, ich q1, cfr 21
** Design Group is seeking a Validation Engineer with a focus on pharmaceutical compliance and project experience. The role emphasizes strong communication skills and offers an environment conducive to professional growth within a collaborative team. **

Job Summary

  • You will join our Regulatory Compliance Practice and partner with seasoned leaders, technical specialists, and subject matter experts to deliver the highest quality solutions to our clients with consistency and accuracy.
  • Responsible for developing and executing a variety of validation and FDA compliance related documents/protocols for pharmaceutical equipment, traveling to top clients across the country.
  • Our culture and commitment to our people is what sets us apart, fostering an environment of mutual respect, integrity, and unconditional interest in the individual and collective success of our professionals.

Matching Summary

Match Score: 75

** Design Group is seeking a Validation Engineer with a focus on pharmaceutical compliance and project experience. The role emphasizes strong communication skills and offers an environment conducive to professional growth within a collaborative team. **

Skills & Requirements

Must-have

  • Validation and FDA compliance
  • FAT, SAT, IQ, OQ documentation
  • QMS procedures, ICH Q1, CFR 21
  • Pharmaceutical or medical device environments
  • Strong technical writing skills
  • Microsoft Office, Microsoft Project, AutoCAD

Nice-to-have

  • Authoring CAPA's, deviations, SOP's
  • Interpersonal skills
  • Flexibility with tasks

Key Requirements

  • Minimum of 3 years project experience with validation
  • Minimum of 3 years project experience in pharmaceutical/medical device
  • B.S. in Bioengineering, Biomedical Engineering, Chemical Engineering, or related technical degree

Work Rights

Not specified

Tailored Resume

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