CQV Engineer

CQV Engineer

Leeds Temporary 36000 - 60000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Join our team as a CQV Engineer, focusing on quality and validation in pharmaceutical manufacturing.
  • Company: Be part of a global leader in pharmaceutical manufacturing, driving innovation in gene therapies.
  • Benefits: Enjoy a 9-month contract with opportunities for growth and development in a dynamic environment.
  • Why this job: Make a real impact in healthcare while working on cutting-edge projects in a collaborative culture.
  • Qualifications: Ideal candidates should have relevant engineering experience and a passion for quality assurance.
  • Other info: This role is part of a large-scale CAPEX investment programme, offering exciting challenges.

The predicted salary is between 36000 - 60000 £ per year.

Our client, a global CDMO in pharmaceutical manufacturing, is recruiting for a CQV Engineer to join their new and exciting large-scale CAPEX investment programme. With a mission to provide process development and cGMP production in cell culture, microbial fermentation, and gene therapies, this is an outstanding opportunity to make a genuine contribution.

CQV Engineer employer: QCS Staffing

As a leading global CDMO in pharmaceutical manufacturing, our company offers an exceptional work environment in Yorkshire, where innovation meets collaboration. Employees benefit from a strong focus on professional development, competitive remuneration, and a supportive culture that values contributions to cutting-edge projects in cell culture and gene therapies. Join us to be part of a dynamic team dedicated to making a meaningful impact in the industry.
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Contact Detail:

QCS Staffing Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land CQV Engineer

✨Tip Number 1

Familiarise yourself with the specific requirements of CQV engineering in the pharmaceutical sector. Understanding cGMP regulations and how they apply to process validation will give you a significant edge during interviews.

✨Tip Number 2

Network with professionals in the pharmaceutical manufacturing field, especially those involved in CAPEX projects. Attend industry events or join relevant online forums to make connections that could lead to valuable insights or referrals.

✨Tip Number 3

Prepare to discuss your previous experience with large-scale projects, particularly in cell culture or microbial fermentation. Be ready to share specific examples of how you've contributed to successful CQV processes in past roles.

✨Tip Number 4

Research our company, StudySmarter, and understand our mission and values. Being able to articulate how your skills align with our goals will demonstrate your genuine interest in the position and help you stand out as a candidate.

We think you need these skills to ace CQV Engineer

Commissioning and Qualification Expertise
Knowledge of cGMP Regulations
Validation Protocol Development
Risk Assessment Skills
Technical Writing Skills
Project Management
Attention to Detail
Problem-Solving Skills
Collaboration and Teamwork
Process Improvement Techniques
Data Analysis
Understanding of Pharmaceutical Manufacturing Processes
Adaptability to Changing Environments
Effective Communication Skills

Some tips for your application 🫡

Understand the Role: Familiarise yourself with the responsibilities of a CQV Engineer, especially in the context of pharmaceutical manufacturing. Highlight your understanding of cGMP processes and CAPEX investment programmes in your application.

Tailor Your CV: Make sure your CV reflects relevant experience in process development, cell culture, microbial fermentation, or gene therapies. Use specific examples to demonstrate your skills and achievements in these areas.

Craft a Compelling Cover Letter: Write a cover letter that not only outlines your qualifications but also expresses your enthusiasm for the role and the company. Mention how your background aligns with their mission and how you can contribute to their projects.

Proofread Your Application: Before submitting, carefully proofread your application materials. Check for spelling and grammatical errors, and ensure that all information is clear and concise. A polished application reflects your attention to detail.

How to prepare for a job interview at QCS Staffing

✨Understand the Role

Make sure you have a solid grasp of what a CQV Engineer does, especially in the context of pharmaceutical manufacturing. Familiarise yourself with concepts like cGMP, process development, and CAPEX investment programmes, as these will likely come up during your interview.

✨Showcase Relevant Experience

Prepare to discuss your previous experience in CQV or related fields. Highlight specific projects where you contributed to process validation or compliance, and be ready to explain how those experiences can benefit the company’s current initiatives.

✨Ask Insightful Questions

Prepare thoughtful questions about the company's current projects and future goals. This shows your genuine interest in the role and helps you understand how you can contribute to their mission in cell culture and gene therapies.

✨Demonstrate Teamwork Skills

Collaboration is key in large-scale projects. Be ready to share examples of how you've successfully worked within a team, particularly in high-pressure environments, to achieve project goals. This will illustrate your ability to fit into their team dynamic.

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