Validation Engineer

Katalyst Healthcares & Life Sciences

Apply to this job
North Haven, CT, us on site Until 8/22/2026 H-1B sponsor history First posted July 26, 2025 Last posted July 26, 2025
Job description
  • Katalyst Healthcares & Life Sciences is hiring entry level candidates for several positions for contract research in Clinical trials of drugs, biologics and medical devices.
  • We have a few immediate job opportunities available in Drug Safety and Pharmacovigilance and Clinical Research field. We work with University hospitals, pharmaceutical companies and recruiting partners.

 

Responsibilities:

  • As a Validation Engineer within the Mold & Capital Tooling Organization, you'll play a pivotal role on a global enterprise team, collaborating with various sites around the world. In this role, you'll facilitate or perform critical validation & qualification activities, ensuring the seamless release of high-quality injection molded components that drive our mission forward.
  • Ensure proper qualification and validation of suppliers and their processes, ensuring supplier meets the requirements for producing high-quality, reliable products.
  • Developing and executing validation plans, conducting audits, and managing the overall PPAP process to ensure compliance with ISO 13485/ Medical standards.
  • Write, review and approve validation change controls and validation protocols IQ OQ PQ PV standard operating procedures, standard calibration methods, standard test methods, specifications CAPAs and exception reports.
  • Strong documentation skills - Accurately recording and managing validation processes in compliance with internal SOPs and external regulations.
  • Review test results and measurements to identify discrepancies.
    SPC (Statistical Process Control).
  • Knowledge on ISO 13485, FDA GMP, ISO 14971, FDA CFR 820.
  • Clean Room experience and medical prod mfg exp (added advantage).
  • Communicates with stakeholders, obtains stakeholder engagement to ensure the end products or processes will solve the business problems.

Requirements:

  • Bachelor's degree with a minimum of 5-7 years of experience in a regulated environment, OR an advanced degree with a minimum of 3 years of experience.
  • Minimum of 5 years of professional experience in a relevant field.
  • Experience with Agile PLM and SAP or BPCS ERP systems.
  • Experience with CAD model with use of Solid works or AutoCAD.
  • Experience with NPI and design transfers deliverables for injection moulded components.
  • Experience within highly regulated industry.
  • Hands on experience within production and enterprise environment.

All your information will be kept confidential according to EEO guidelines.

About this role

Summary

Perform validation, qualification, and validation activities for medical device manufacturing.

Job title

Validation Engineer

Experience level

5+ years or 3+ years with advanced degree

Industry

medical devices

Location requirements

North Haven, CT, on-site; remote not specified

Salary

Not specified

Visa sponsorship

H-1B sponsor history

Management role

No

Skills & keywords

Required skills

validationqualificationISO 13485FDA GMPISO 14971FDA CFR 820SPCvalidation protocolsauditvalidation change controls

Preferred skills

Clean Room experiencemedical product manufacturingAgile PLMSAPBPCS ERPCADSolidWorksAutoCADNPIdesign transfers

Specializations

validationqualificationISO 13485medical standardsvalidation protocols
Locations

Structured locations inferred from the posting.

North Haven, CT 06473, USA

On-site City
Related searches