At a Glance
- Tasks: Conduct risk analysis and validation plans for pharma automation projects.
- Company: Join Syspro Automation, a global leader in GMP engineering.
- Benefits: Permanent contract, professional development, and continuous training.
- Other info: Dynamic environment with opportunities for growth and learning.
- Why this job: Make a real impact in the biotech industry with a skilled team.
- Qualifications: 3+ years in CSV validation and strong documentation skills.
The predicted salary is between 40000 - 50000 € per year.
In Syspro Automation we are looking for CSV (Computerized System Validation) Engineers to join a multidisciplinary team working in challenging automation projects within a GMP environment. Syspro Automation is an engineering company focused on GMP Automation, working globally with offices in Spain, Portugal, Switzerland and the United States.
Main responsibilities:
- Conduct risk analysis and define validation plans for various process equipments in the pharmaceutical industry.
- Review documentation of the equipments to ensure compliance with the validation plan.
- Define, execute and document qualification tests.
- Manage and document deviations and changes.
Required skills and experience:
- Minimum of 3 years of experience in CSV validation.
- Strong skills in managing and creating documentation (Microsoft Word and Excel).
- Excellent communication skills and proactive attitude.
- Ability to work independently and as part of a team.
- Experience within the biotech industry with knowledge of current Good Manufacturing Procedures (cGMP).
- English level C1 or better.
Skills that would be a plus:
- Spanish language is a plus.
We offer:
- Permanent contract.
- Integration into a young and highly skilled team.
- Opportunities for professional development and continuous training.
Validation Engineer - Pharma employer: Syspro Automation
At Syspro Automation, we pride ourselves on being an excellent employer, offering a dynamic work culture that fosters collaboration and innovation within our multidisciplinary teams. Located in a vibrant global environment, we provide our employees with permanent contracts, continuous training, and ample opportunities for professional growth, making it an ideal place for those seeking meaningful careers in the pharmaceutical automation sector.
StudySmarter Expert Advice🤫
We think this is how you could land Validation Engineer - Pharma
✨Tip Number 1
Network like a pro! Reach out to your connections in the pharma and biotech industries. Attend industry events or webinars, and don’t be shy about introducing yourself. You never know who might have the inside scoop on job openings!
✨Tip Number 2
Prepare for interviews by brushing up on your technical knowledge. Make sure you can confidently discuss CSV processes and cGMP regulations. Practise common interview questions with a friend or in front of the mirror to nail that confidence!
✨Tip Number 3
Showcase your documentation skills! Bring examples of your previous work to the interview, especially if it highlights your ability to manage and create documentation. This will demonstrate your attention to detail and expertise in the field.
✨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 are proactive about their job search. Let’s get you on board with Syspro Automation!
We think you need these skills to ace Validation Engineer - Pharma
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Validation Engineer role. Highlight your experience in CSV validation and any relevant projects you've worked on in the pharma or biotech industry. We want to see how your skills match what we're looking for!
Showcase Your Documentation Skills:Since managing and creating documentation is key for this role, don’t forget to mention your proficiency with Microsoft Word and Excel. Give examples of how you've successfully documented processes or managed deviations in past roles.
Communicate Clearly:Your communication skills are crucial, so make sure your application is clear and concise. Use straightforward language and avoid jargon unless it’s relevant to the role. We appreciate a proactive attitude, so let that shine through in your writing!
Apply Through Our Website:We encourage you to apply directly through our website. It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it shows you’re keen on joining our team at Syspro Automation!
How to prepare for a job interview at Syspro Automation
✨Know Your CSV Inside Out
Make sure you brush up on your Computerized System Validation knowledge. Be ready to discuss specific methodologies and tools you've used in past projects, especially in a GMP environment. This will show that you’re not just familiar with the concepts but have practical experience.
✨Documentation is Key
Since the role involves managing and creating documentation, prepare examples of how you've handled documentation in previous roles. Bring along samples or be ready to discuss your process for ensuring compliance with validation plans. This will demonstrate your attention to detail and organisational skills.
✨Show Off Your Communication Skills
Excellent communication is crucial in this role. Practice explaining complex validation processes in simple terms, as you might need to communicate with team members from different backgrounds. Think about times when your communication made a difference in a project.
✨Be Ready for Team Dynamics
This position requires both independent work and teamwork. Prepare to discuss how you’ve successfully collaborated with others in the past, especially in multidisciplinary teams. Highlight any experiences where you took the initiative or helped resolve conflicts.
