At a Glance
- Tasks: Support project management and validation across diverse engineering projects.
- Company: Dynamic engineering firm focused on innovation and collaboration.
- Benefits: Competitive salary, travel opportunities, and hands-on experience in the field.
- Other info: Exciting career growth with opportunities to work on cutting-edge projects.
- Why this job: Join a team making a real impact in the engineering and validation space.
- Qualifications: Degree in engineering or science, project management skills, and technical writing ability.
The predicted salary is between 30000 - 40000 £ per year.
Our client is looking to appoint an experienced Project Validation Technician to help deliver their extended business portfolio of project services and further support our clients and suppliers. In this role, you will be responsible for providing project, technical, scientific and validation support across the business and directly to our network of customers and suppliers. As a CQV team member, you will support the delivery of equipment, process, validation, and business projects. This role provides the right candidate with an exciting opportunity to work ‘hands-on’, across an extensive range of project services and an array of equipment and process types.
Key Responsibilities
- Responsible for direct customer support and OPEX project management - liaise between all parties during OPEX equipment build and report on progress.
- Completion of project documentation and tasks in line with our business’s internal templates, processes and GPG’s.
- Management & completion of tasks (e.g. Protean) & providing contract managers (TSE’s) with information to ensure timely invoicing for site work performed.
- Organise shipping as required, monitor progress, and keep customer advised of likely delivery date(s).
- Supporting planning and sitework activities.
- Responsible execution of delegated project services (such as RTM, technical reviews, reports, and other technical & commercial opportunities).
- Provide technical writing support to our wider team, suppliers, and customers.
- Reasonable Supplier & Customer support visits as deemed necessary – e.g. FAT validation support, project, or validation meetings.
- Punchlist management across all equipment supply.
- ~25% ‘On site’ execution of validation documentation including protocols, summary reports & other lifecycle documents, as required.
- Co-ordinating & supporting validation testing of equipment such as autoclaves, process & utilities.
- Analysing, interpreting and reporting on validation testing against acceptance criteria.
- Supporting the Team in other value add deliverables, such as HAZOP, FMECA, and other similar activities.
- Be accountable, customer focused & collaborative, reflecting the company’s goals and values.
- Contribute to business initiatives & actions (e.g. quality system, technical research, improvements & promotion, continuous improvements, health & safety).
- Other duties as assigned.
Key skills and experience
- Project management experience.
- Having the right attitude and drive to meet objectives and targets.
- Reasonable travel to customer and supplier sites will be required.
- Technical writing with an excellent understanding of ‘Plain English’ writing technique.
- Relevant Degree or comparable qualification in an engineering, science, or validation discipline.
- Relevant experience supporting aseptic manufacturing or clean utilities.
- Ability to read and interpret documents such as technical drawings, process specifications, safety protocols, company policies, and procedure manuals.
- Demonstrate a structured approach to documentation planning & design.
- A clear understanding of equipment validation lifecycles in the pharma industry.
- Ability to work on your own initiative, to pre-determined schedules, and execute validation studies.
- Ability to successfully manage concurrent deliverables on time.
- Ability to converse with, present on and interrogate customer/supplier validation requirements.
- Ability to analyse and organise complex material with attention to detail.
- A demonstrated proficiency in the standard MS packages.
- Organised, adaptable & flexible.
Project Engineer (Netherlands) in Surrey employer: Cpl Life Sciences
Join a dynamic team in the Netherlands where your expertise as a Project Engineer will be valued and nurtured. Our company fosters a collaborative work culture that prioritises employee growth through continuous learning opportunities and hands-on project involvement. With a focus on innovation and customer satisfaction, we offer a supportive environment that encourages you to make a meaningful impact in the field of project services.
StudySmarter Expert Advice🤫
We think this is how you could land Project Engineer (Netherlands) in Surrey
✨Tip Number 1
Network like a pro! Reach out to industry contacts on LinkedIn or attend local engineering meetups. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching the company and its projects. Show them you’re not just another candidate; you’re genuinely interested in their work and how you can contribute to their success.
✨Tip Number 3
Practice your technical writing skills! Since this role involves documentation, being able to clearly articulate your thoughts will set you apart. Consider drafting some sample reports or protocols to showcase your abilities.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who take that extra step to connect with us directly.
We think you need these skills to ace Project Engineer (Netherlands) in Surrey
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Project Engineer role. Highlight your project management experience and technical writing skills, as these are key for us. Use specific examples that showcase your ability to meet objectives and targets.
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Explain why you're passionate about this role and how your background aligns with our needs. Don’t forget to mention your experience in aseptic manufacturing or clean utilities if you have it!
Showcase Your Technical Skills:We love candidates who can demonstrate their technical prowess. Include any relevant qualifications and experiences that show your understanding of equipment validation lifecycles in the pharma industry. Be clear and concise!
Apply Through Our Website:We encourage you to apply through our website for a smoother application process. It helps us keep track of your application and ensures you don’t miss out on any important updates from us!
How to prepare for a job interview at Cpl Life Sciences
✨Know Your Projects
Before the interview, brush up on your project management experience. Be ready to discuss specific projects you've worked on, especially those involving OPEX management and validation support. This will show that you understand the role's responsibilities and can relate your experience directly to what they need.
✨Technical Writing Skills
Since technical writing is a key part of this role, prepare examples of your writing. Bring along samples of protocols, reports, or any documentation you've created. This will demonstrate your ability to communicate complex information clearly and effectively, which is crucial for the position.
✨Understand Validation Lifecycles
Make sure you have a solid grasp of equipment validation lifecycles in the pharma industry. Be prepared to discuss how you've applied this knowledge in past roles. This will highlight your expertise and show that you're ready to hit the ground running.
✨Show Your Customer Focus
This role requires a customer-focused approach, so think of examples where you've successfully liaised with clients or suppliers. Highlight your ability to keep all parties informed and manage expectations. This will demonstrate that you can maintain strong relationships while delivering on project goals.
