At a Glance
- Tasks: Join a dynamic team to validate automation systems in the pharmaceutical industry.
- Company: Syspro Automation, a global leader in GMP Automation.
- Benefits: Permanent contract, professional development, and continuous training.
- Other info: Be part of a young, skilled team with global opportunities.
- Why this job: Make a real impact in a fast-paced environment with innovative projects.
- Qualifications: 3+ years in CSV validation and strong documentation skills required.
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.
CSV/CQV Validation Engineers employer: Syspro Automation
At Syspro Automation, we pride ourselves on being an excellent employer by fostering a dynamic work culture that encourages innovation and collaboration within our multidisciplinary teams. Our commitment to employee growth is evident through continuous training opportunities and a supportive environment, making it an ideal place for CSV/CQV Validation Engineers to thrive in their careers while contributing to impactful automation projects in the pharmaceutical industry.
StudySmarter Expert Advice🤫
We think this is how you could land CSV/CQV Validation Engineers
✨Tip Number 1
Network like a pro! Reach out to your connections in the biotech and automation sectors. Attend industry events or webinars to meet potential employers and get your name out there.
✨Tip Number 2
Prepare for interviews by brushing up on your technical knowledge and soft skills. Practice common interview questions related to CSV validation and be ready to discuss your experience with GMP environments.
✨Tip Number 3
Showcase your documentation skills! Bring examples of your previous work, like validation plans or qualification tests, to demonstrate your expertise during interviews.
✨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.
We think you need these skills to ace CSV/CQV Validation Engineers
Some tips for your application 🫡
Tailor Your CV:Make sure your CV highlights your experience in CSV validation and any relevant projects you've worked on. We want to see how your skills align with the role, so don’t be shy about showcasing your achievements!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you’re passionate about working in a GMP environment and how your background makes you a perfect fit for our team at Syspro Automation.
Show Off Your Documentation Skills:Since managing and creating documentation is key for this role, include examples of your work with Microsoft Word and Excel. We love seeing how you’ve tackled documentation challenges in the past!
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’s super easy!
How to prepare for a job interview at Syspro Automation
✨Know Your CSV Inside Out
Make sure you brush up on your knowledge of Computerized System Validation. 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 managing and creating documentation is crucial for this role, prepare examples of how you've handled documentation in previous positions. Bring along samples or be ready to discuss your process in detail, particularly with Microsoft Word and Excel.
✨Show Your Team Spirit
Syspro Automation values teamwork, so be prepared to share experiences where you’ve successfully collaborated with others. Highlight your communication skills and proactive attitude, as these are essential for working effectively within a multidisciplinary team.
✨Brush Up on cGMP Knowledge
Familiarise yourself with current Good Manufacturing Procedures (cGMP) and be ready to discuss how they apply to your work. If you have any specific examples of how you've ensured compliance in past roles, make sure to mention them during the interview.
