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- Tasks: Join our team as a CQV Engineer, overseeing automation system validation and documentation.
- Company: Impact Engineering Ltd is a leading automation partner in Dublin, driving digital transformation.
- Benefits: Enjoy a dynamic work environment with opportunities for professional growth and hands-on experience.
- Why this job: Be part of innovative projects that shape the future of automation in the pharmaceutical industry.
- Qualifications: Bachelor’s degree in engineering and 5+ years of relevant experience required.
- Other info: This role is site-based in Northern Ireland, requiring daily on-site presence.
The predicted salary is between 42000 - 84000 £ per year.
Impact Engineering Ltd is a trusted automation partner based in Dublin, focusing on business transformation, digitalisation, automation projects, and targeted automation training. We offer a range of services including consultancy, system upgrades, process optimization, and automation front line support. Our mission is to deliver innovative, cost-competitive, and compliant automation solutions to add value to businesses through digitalization.
This is a site based contract role for a CQV Engineer at our customer site, based in Northern Ireland. This position is a key element of a project team that will be based on site. In this role you will be expected to:
- Take part in the planning, execution, and oversight of CQV activities to ensure that automated systems meet predefined requirements and operate within validated parameters.
- Create and maintain validation documentation, including protocols, test scripts, and validation reports.
- Ensure that all automation systems comply with industry standards, GxP guidelines, and regulatory mandates.
- Maintain accurate and organized documentation for all validation activities, including equipment and software specifications, validation protocols, and records.
- Collaborate with our client to ensure the proper documentation of automated system configurations.
Qualifications & Experience
- Bachelor’s degree in engineering or similar.
- 5+ years working experience as CQV Engineer on Pharmaceutical or Biopharmaceutical projects or comparable experience.
- Experience with DeltaV is preferred.
- On site project experience is essential.
- Ability to work on site every day.
- Ability to interact and communicate with other engineering and business disciplines.
CQV Engineer employer: Impact Engineering
Contact Detail:
Impact Engineering Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land CQV Engineer
✨Tip Number 1
Familiarise yourself with the specific automation systems and tools mentioned in the job description, particularly DeltaV. Having hands-on experience or knowledge about these systems can set you apart during interviews.
✨Tip Number 2
Network with professionals in the pharmaceutical and biopharmaceutical sectors. Attend industry events or join relevant online forums to connect with others who may have insights into the role or the company.
✨Tip Number 3
Prepare to discuss your previous CQV projects in detail. Be ready to explain how you ensured compliance with GxP guidelines and how you handled challenges during validation processes.
✨Tip Number 4
Research Impact Engineering Ltd thoroughly. Understand their mission, values, and recent projects to demonstrate your genuine interest in the company during your interactions with them.
We think you need these skills to ace CQV Engineer
Some tips for your application 🫡
Understand the Role: Before applying, make sure you fully understand the responsibilities of a CQV Engineer as outlined in the job description. Highlight your relevant experience and skills that align with the requirements.
Tailor Your CV: Customise your CV to reflect your experience in CQV activities, particularly in pharmaceutical or biopharmaceutical projects. Emphasise your familiarity with DeltaV and any on-site project experience you have.
Craft a Compelling Cover Letter: Write a cover letter that showcases your passion for automation and your understanding of the industry standards and GxP guidelines. Mention specific examples from your past work that demonstrate your ability to meet the role's requirements.
Proofread Your Application: Before submitting, carefully proofread your application materials for any spelling or grammatical errors. A polished application reflects your attention to detail, which is crucial for a CQV Engineer.
How to prepare for a job interview at Impact Engineering
✨Know Your CQV Fundamentals
Make sure you have a solid understanding of CQV principles and practices. Be prepared to discuss your experience with validation documentation, protocols, and test scripts, as these are crucial for the role.
✨Familiarise Yourself with DeltaV
Since experience with DeltaV is preferred, brush up on your knowledge of this system. Be ready to explain how you've used it in past projects and how it relates to CQV activities.
✨Highlight Your On-Site Experience
This role requires daily on-site presence, so emphasise your previous on-site project experience. Share specific examples of how you collaborated with teams and managed tasks in a site-based environment.
✨Understand Industry Standards
Be well-versed in GxP guidelines and regulatory mandates relevant to the pharmaceutical and biopharmaceutical sectors. Prepare to discuss how you ensure compliance in your work and the importance of these standards.
