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Sr Validation Engineer

  • ... Posted on: Oct 07, 2024
  • ... Intellectt INC
  • ... Maplewood, Minnesota
  • ... Salary: Not Available
  • ... Full-time

Sr Validation Engineer   

Job Title :

Sr Validation Engineer

Job Type :

Full-time

Job Location :

Maplewood Minnesota United States

Remote :

No

Jobcon Logo Job Description :

Job Title: Sr Validation Engineer

Location: Plymouth, MN | Princeton, NJ | Irving, TX (W2 Contract)

Key Responsibilities:

  • Lead the development and execution of validation protocols, including IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) for equipment and processes.
  • Design, plan, and implement validation strategies for new and existing processes to ensure they meet regulatory requirements (FDA, ISO 13485, EU MDR, etc.).
  • Collaborate with cross-functional teams (Quality, Engineering, Production) to identify and mitigate risks through validation activities.
  • Author and review validation plans, protocols, and reports, ensuring accuracy and compliance with regulatory standards and company policies.
  • Conduct process validations, method validations, cleaning validations, and equipment qualifications.
  • Investigate deviations and non-conformances that occur during validation activities and develop corrective and preventive actions (CAPAs).
  • Support regulatory submission activities by providing validation documentation and technical support.
  • Maintain up-to-date knowledge of industry regulations and standards and ensure all validation processes comply with them.
  • Participate in the continuous improvement of validation processes, including identifying areas for efficiency and compliance enhancement.

Required Qualifications:

  • Bachelor's degree in Engineering, Life Sciences, or a related field.
  • 4+ years of experience in validation engineering within the medical device industry.
  • In-depth knowledge of FDA regulations, ISO 13485, and other relevant medical device standards.
  • Experience with process validation, equipment qualification, method validation, and cleaning validation.
  • Strong technical writing skills for developing validation protocols, reports, and SOPs.
  • Proficiency in validation tools and statistical analysis software.
  • Ability to work in a regulated environment and maintain strict adherence to quality standards.
  • Excellent communication skills and ability to work collaboratively with cross-functional teams.

Jobcon Logo Position Details

Posted:

Oct 07, 2024

Employment:

Full-time

Salary:

Not Available

Snaprecruit ID:

SD-CIE-50cfc4605ba563ffa2cb1efeb28d1036158d2c5ed0028a7f4f8e621e831d9361

City:

Maplewood

Job Origin:

CIEPAL_ORGANIC_FEED

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Job Title: Sr Validation Engineer

Location: Plymouth, MN | Princeton, NJ | Irving, TX (W2 Contract)

Key Responsibilities:

  • Lead the development and execution of validation protocols, including IQ (Installation Qualification), OQ (Operational Qualification), and PQ (Performance Qualification) for equipment and processes.
  • Design, plan, and implement validation strategies for new and existing processes to ensure they meet regulatory requirements (FDA, ISO 13485, EU MDR, etc.).
  • Collaborate with cross-functional teams (Quality, Engineering, Production) to identify and mitigate risks through validation activities.
  • Author and review validation plans, protocols, and reports, ensuring accuracy and compliance with regulatory standards and company policies.
  • Conduct process validations, method validations, cleaning validations, and equipment qualifications.
  • Investigate deviations and non-conformances that occur during validation activities and develop corrective and preventive actions (CAPAs).
  • Support regulatory submission activities by providing validation documentation and technical support.
  • Maintain up-to-date knowledge of industry regulations and standards and ensure all validation processes comply with them.
  • Participate in the continuous improvement of validation processes, including identifying areas for efficiency and compliance enhancement.

Required Qualifications:

  • Bachelor's degree in Engineering, Life Sciences, or a related field.
  • 4+ years of experience in validation engineering within the medical device industry.
  • In-depth knowledge of FDA regulations, ISO 13485, and other relevant medical device standards.
  • Experience with process validation, equipment qualification, method validation, and cleaning validation.
  • Strong technical writing skills for developing validation protocols, reports, and SOPs.
  • Proficiency in validation tools and statistical analysis software.
  • Ability to work in a regulated environment and maintain strict adherence to quality standards.
  • Excellent communication skills and ability to work collaboratively with cross-functional teams.

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