At a Glance
- Tasks: Conduct risk analysis and define validation plans for pharmaceutical process equipment.
- Company: Join Syspro Automation, a global leader in GMP Automation.
- Benefits: Permanent contract, professional development, and continuous training.
- Other info: Work in a dynamic environment with opportunities for growth.
- Why this job: Be part of a young, skilled team making a difference in the biotech industry.
- 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.
Validation Consultant 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. Our commitment to employee growth is evident through continuous training opportunities and a supportive environment, making it an ideal place for Validation Consultants to thrive in the fast-paced pharmaceutical industry. With a permanent contract and the chance to work on challenging automation projects globally, we provide a rewarding career path for those looking to make a meaningful impact.
StudySmarter Expert Advice🤫
We think this is how you could land Validation Consultant
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, especially those who work in GMP environments. A friendly chat can lead to insider info about job openings or even a referral.
✨Tip Number 2
Prepare for interviews by brushing up on your technical knowledge and soft skills. Be ready to discuss your experience with CSV validation and how you’ve tackled challenges in past projects.
✨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 compliance documentation.
✨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 Validation Consultant
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Validation Consultant role. Highlight your experience in CSV validation and any relevant projects you've worked on. We want to see how your skills match what we're looking for!
Showcase Your Documentation Skills:Since managing and creating documentation is key, include examples of your work with Microsoft Word and Excel. We love seeing how you’ve handled documentation in past roles, especially in a GMP environment.
Communicate Clearly:Your communication skills are crucial, so make sure your application is clear and concise. Use straightforward language and structure your application well. We appreciate a proactive attitude, so let that shine through!
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!
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 your previous work. Bring along samples of validation plans or qualification tests you've executed. This will demonstrate your attention to detail and your ability to comply with cGMP standards.
✨Show Off Your Communication Skills
Practice articulating your thoughts clearly and concisely. You might be asked to explain complex validation processes, so being able to communicate effectively is crucial. Consider doing mock interviews with a friend to refine your delivery.
✨Be Ready for Team Dynamics
Syspro Automation values teamwork, so be prepared to discuss how you’ve collaborated with others in past roles. Think of examples where you’ve worked independently as well as part of a team, and how you managed any challenges that arose.
