At a Glance
- Tasks: Lead a team of CQV Engineers and manage project delivery from start to finish.
- Company: Join a dynamic company with 1000+ employees specializing in complex infrastructure projects.
- Benefits: Enjoy a bonus, car allowance, matched pension, life assurance, and generous holiday.
- Why this job: Be part of impactful projects in the pharmaceutical sector while mentoring and guiding others.
- Qualifications: Experience in Pharmaceutical Manufacturing and knowledge of EU GMP standards required.
- Other info: This is a permanent, full-time role based in the North East, UK.
The predicted salary is between 43200 - 72000 £ per year.
Lead CQV Engineer – EPCm – North East Position: Lead CQV Engineer Location: North East, UK Salary: Negotiable – dependant on experience Type: Permanent, Full-Time About the Company With over 1000+ employees across 14 locations in the UK and Europe, they partner with companies Globally specialising in complex infrastructure, process and built environments across the full project life cycle, from design and construction to handover and operational management. Job Summary As the CQV Lead you will be responsible for managing a small team of CQV Engineers and deliver CQV services as part of the framework agreement for their client. The role will be responsible for all the CQV stages of the project from initiation to handover to the client’s team at the completion of OQ. * Deliver CQV Services on time and on budget. * Support, train, mentor, and provide guidance to commissioning and validation specialists/engineers in the delivery of CQV services. * Develop systems, procedures and process’ to ensure consistency of delivery of services. * Write and manage others in the preparation of C/Q/V documents following established standards and templates. * Execute and manage others in the execution of C/Q/V protocols following established standards and templates. Qualifications & Skills * Significant experience of working in the Pharmaceutical Manufacturing sector * Knowledge of EU GMP Annex 1: Manufacture of Sterile Medicinal Products * Understanding of equipment used in the Manufacture of Sterile Medicinal Products. * Strong demonstrable communication and interpersonal skills, particularly the ability to influence and negotiate both internally and externally * Ability to work well within a multi-disciplinary environment (engineers, designers etc.) in delivering services to satisfy the agreed brief Benefits * Company bonus of up to 5% * Company Car / Car Allowance * Up to 6% matched pension * Life Assurance * 25 days holiday + bank holidays * Private Medical
Lead CQV Engineer employer: Adepto Technical Recruitment Ltd
Contact Detail:
Adepto Technical Recruitment Ltd Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Lead CQV Engineer
✨Tip Number 1
Make sure to highlight your experience in the Pharmaceutical Manufacturing sector during networking events or conversations. This will help you connect with industry professionals who can provide insights or referrals.
✨Tip Number 2
Familiarize yourself with EU GMP Annex 1 and the specific equipment used in the manufacture of sterile medicinal products. This knowledge will not only boost your confidence but also demonstrate your expertise during interviews.
✨Tip Number 3
Engage with online forums or groups related to CQV engineering and pharmaceutical manufacturing. Sharing your thoughts and asking questions can help you build a network and learn about potential job openings.
✨Tip Number 4
Consider reaching out to current or former employees of the company to gain insights into their work culture and expectations. This information can be invaluable when preparing for interviews and tailoring your approach.
We think you need these skills to ace Lead CQV Engineer
Some tips for your application 🫡
Understand the Role: Make sure to thoroughly read the job description for the Lead CQV Engineer position. Understand the responsibilities and qualifications required, and think about how your experience aligns with these.
Tailor Your CV: Customize your CV to highlight relevant experience in the Pharmaceutical Manufacturing sector, particularly focusing on CQV processes and any leadership roles you've held. Use specific examples that demonstrate your skills in managing teams and delivering projects.
Craft a Strong Cover Letter: Write a compelling cover letter that outlines your passion for the role and the company. Mention your significant experience with EU GMP Annex 1 and how you can contribute to the team’s success. Be sure to convey your communication and interpersonal skills.
Review and Submit: Before submitting your application, review all documents for clarity and accuracy. Ensure that your CV and cover letter are free of errors and reflect your best professional self. Submit your application through our website to ensure it reaches the right people.
How to prepare for a job interview at Adepto Technical Recruitment Ltd
✨Showcase Your CQV Expertise
Make sure to highlight your significant experience in the Pharmaceutical Manufacturing sector. Be prepared to discuss specific projects where you successfully delivered CQV services, emphasizing your understanding of EU GMP Annex 1 and the equipment used in sterile product manufacturing.
✨Demonstrate Leadership Skills
As a Lead CQV Engineer, you'll be managing a team. Share examples of how you've supported, trained, or mentored others in previous roles. This will show your ability to lead and develop a team effectively.
✨Prepare for Technical Questions
Expect technical questions related to CQV protocols and documentation. Familiarize yourself with established standards and templates, and be ready to explain how you have implemented these in past projects.
✨Communicate Effectively
Strong communication skills are crucial for this role. Practice articulating your thoughts clearly and concisely. Be prepared to discuss how you've influenced and negotiated with stakeholders in a multi-disciplinary environment.