Process Validation Engineer

Vantive; Castlebar; On-site; CAD 50,000 - 90,000; Full time

Job summary

Join a forward-thinking company dedicated to transforming vital organ therapies and enhancing the dialysis experience. As a Process Validation Engineer, you'll be at the forefront of quality assurance in manufacturing, playing a key role in ensuring compliance and excellence. With a commitment to innovation and patient care, this position offers a unique opportunity to grow your career while making a meaningful impact on lives worldwide. Enjoy competitive benefits, a supportive team, and a culture that values courage and focus. If you're eager to learn and develop, this is the place for you!

Benefits

25 days annual leave

Competitive salary

Extensive benefits package

Sports & social activities

Qualifications

• Degree in Science/Engineering or equivalent is required.
• Process validation experience is desirable.

Responsibilities

• Author validation protocols, reports, and risk assessments.
• Lead projects to ensure they are executed in a controlled manner.

Skills

Critical thinking

Problem-solving

Teamwork

Education

Degree in Science/Engineering

Tools

Trackwise 8

Job description

1 week ago Be among the first 25 applicants

Vantive is a vital organ therapy company on a mission to extend lives and expand possibilities for patients and care teams everywhere. For 70 years, our team has driven meaningful innovations in kidney care. As we build on our legacy, we are deepening our commitment to elevating the dialysis experience through digital solutions and advanced services, while looking beyond kidney care and investing in transforming vital organ therapies. Greater flexibility and efficiency in therapy administration for care teams, and longer, fuller lives for patients— that is what Vantive aspires to deliver.

We believe Vantive will not only build our leadership in the kidney care space, but also offer meaningful work to those who join us. At Vantive, you will become part of a community of people who are focused, courageous, and don’t settle for mediocrity. Each of us is driven to help improve patients’ lives worldwide. Join us in advancing our mission to extend lives and expand possibilities.

CV must be attached to your application

Process Validation Engineer

We are actively searching for a Process Validation Engineer to join our team based at our Castlebar, Co. Mayo site. The Castlebar and Swinford facilities employ more than 1300 staff, operating 24/7.

You will play a key role in the Quality and Process within our manufacturing, supporting equipment and processes critical to extending lives and expanding possibilities.

Working in the Process Validation Department, the successful candidate will be self-driven, motivated, willing to learn, and eager to develop their career as a Process Validation Engineer. Training and mentorship will be provided.

What will you do?

• Author validation protocols, reports, and risk assessments
• Review engineering trials and product development documentation
• Complete Trackwise 8 validation and risk assessments
• Technical approval of validation documentation
• Lead projects to ensure they are executed in a controlled and compliant manner
• Provide status updates on projects
• Deliver presentations and manage projects

Your Qualities

• Degree in Science/Engineering or equivalent
• Process validation experience is desirable
• Knowledge of EU GMP and FDA regulatory requirements
• Critical thinking and problem-solving skills
• Solid decision-making abilities
• Ability to work well within a team

What Can Vantive Offer To You

• 25 days annual leave, with potential for 4 additional days per year
• Competitive salary
• Extensive benefits package
• Sports & social activities

Reasonable Accommodation

Vantive is committed to providing reasonable accommodations to individuals with disabilities. If you need accommodations during the application or interview process, please click on the link here and let us know your request along with contact information. Form Link

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Seniority level

• Entry level

Employment type

• Full-time

Job function

• Quality Assurance

Industries

• Medical Equipment Manufacturing