At a Glance
- Tasks: Join a dynamic team to ensure the successful commissioning of biopharmaceutical systems.
- Company: Be part of a global leader in pharmaceutical manufacturing focused on innovative therapies.
- Benefits: Enjoy a 9-month contract with opportunities for growth and hands-on experience.
- Other info: This role offers a chance to work on cutting-edge CAPEX investment programmes.
- Why this job: Make a real impact in the biopharmaceutical industry while working on exciting projects.
- Qualifications: Bring your extensive experience with process equipment and expansion projects.
The predicted salary is between 42000 - 60000 £ per year.
Job Description
Our client, aglobal CDMO in pharmaceutical manufacturing, is recruiting for aCQV 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 make a genuine contribution to the biopharmaceutical industry.
Responsibilities include:
- Liaise with CQV PM and Lead Scheduler.
- Ensure Commissioning readiness of all Systems to support Equipment Start-up and IOQ Testing.
- Lead CQV interface with EIDA / or Master Project Database equivalent system, ensure full traceability at all times for all systems within the fill finish building
- Liaise with all Project Groups to ensure all Systems are managed appropriately for the Project Lifecycle.
- Lead execution of all CQV deliverables; IOQ, field execution
- Responsible for the generation of Test Protocols for the verification of process equipment.
- Execution of the protocols utilising data generated by equipment vendors.
- Execution of any remaining testing requirements.
- Oversight of vendor testing.
- Generation of reports.
- Extensive experience including experience with expansion projects.
- Experience working with process equipment including;filtration systems, chromatography equipment and consumables, bioreactors, cell culture systems, mixing systems, bioprocessing
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CQV Engineer in Redcar employer: QCS Staffing
As a leading global CDMO in pharmaceutical manufacturing, our company offers CQV Engineers an exceptional opportunity to contribute to groundbreaking projects in the biopharmaceutical sector. Located in Yorkshire, we foster a collaborative work culture that prioritises employee growth and development, providing access to cutting-edge technology and training. With a strong commitment to innovation and excellence, we ensure our team members are well-supported and empowered to make a meaningful impact in their roles.
StudySmarter Expert Advice🤫
We think this is how you could land CQV Engineer in Redcar
✨Tip Number 1
Familiarise yourself with the specific equipment mentioned in the job description, such as filtration systems and bioreactors. Having a solid understanding of these technologies will help you speak confidently about your experience during interviews.
✨Tip Number 2
Network with professionals in the pharmaceutical manufacturing industry, especially those who have worked on CAPEX investment programmes. Engaging with them can provide insights into the role and may even lead to referrals.
✨Tip Number 3
Prepare to discuss your previous experiences with commissioning and qualification processes. Be ready to share specific examples of how you've ensured compliance and traceability in past projects.
✨Tip Number 4
Stay updated on the latest trends and regulations in the biopharmaceutical industry. This knowledge will not only enhance your discussions but also demonstrate your commitment to the field during interviews.
We think you need these skills to ace CQV Engineer in Redcar
Some tips for your application 🫡
Understand the Role:Read the job description thoroughly to understand the responsibilities and key requirements of the CQV Engineer position. Tailor your application to highlight relevant experience in commissioning, qualification, and validation processes.
Highlight Relevant Experience:In your CV and cover letter, emphasise your extensive experience with process equipment such as filtration systems, chromatography equipment, and bioreactors. Provide specific examples of past projects that align with the role's requirements.
Craft a Strong Cover Letter:Write a compelling cover letter that not only outlines your qualifications but also expresses your enthusiasm for contributing to the biopharmaceutical industry. Mention your familiarity with cGMP production and any relevant CAPEX investment experience.
Proofread Your Application:Before submitting, carefully proofread your CV and cover letter for any spelling or grammatical errors. A polished application reflects attention to detail, which is crucial for a CQV Engineer role.
How to prepare for a job interview at QCS Staffing
✨Know Your CQV Fundamentals
Make sure you have a solid understanding of Commissioning, Qualification, and Validation (CQV) principles. Be prepared to discuss your experience with equipment like filtration systems and bioreactors, as well as how you've ensured compliance with cGMP standards in past projects.
✨Demonstrate Project Management Skills
Since the role involves liaising with various project groups, highlight your project management experience. Discuss specific examples where you successfully coordinated with different teams to ensure project milestones were met, especially in large-scale CAPEX investment programmes.
✨Prepare for Technical Questions
Expect technical questions related to the equipment and processes you'll be working with. Brush up on your knowledge of chromatography equipment, mixing systems, and bioprocessing techniques, and be ready to explain how you've applied this knowledge in practical scenarios.
✨Showcase Your Problem-Solving Abilities
Be ready to discuss challenges you've faced in previous roles and how you overcame them. This could include issues during equipment start-up or testing phases. Demonstrating your analytical thinking and ability to troubleshoot will impress interviewers.
