At a Glance
- Tasks: Conduct risk analysis and define validation plans in the pharma industry.
- Company: Join Syspro Automation, a global leader in GMP Automation.
- Benefits: Permanent contract, professional development, and a young, skilled team.
- Other info: Opportunities for continuous training and growth in your career.
- Why this job: Make a real impact in challenging automation projects within a dynamic environment.
- 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 | Pharma - Hybrid 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 hybrid working model allows for flexibility while working on challenging automation projects in the pharmaceutical industry, and we are committed to the professional growth of our employees through continuous training and development opportunities. Join us in a vibrant environment where your expertise in CSV validation will be valued and where you can make a meaningful impact in the field of GMP Automation.
StudySmarter Expert Advice🤫
We think this is how you could land Validation Consultant | Pharma - Hybrid
✨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 researching Syspro Automation and understanding their projects. Tailor your answers to show how your experience in CSV validation aligns with their needs. We want to see your passion for GMP automation shine through!
✨Tip Number 3
Practice makes perfect! Conduct mock interviews with friends or mentors to refine your responses. Focus on articulating your experience with risk analysis and documentation management, as these are key skills for the role.
✨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 the initiative to engage directly with us.
We think you need these skills to ace Validation Consultant | Pharma - Hybrid
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.
Be Proactive in Your Cover Letter:Use your cover letter to show off your proactive attitude. Share specific examples of how you've tackled challenges in previous roles, particularly in the biotech industry. We appreciate candidates who take initiative!
Apply Through Our Website:Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. We can’t wait to see what you bring to the table!
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
Excellent communication is crucial for this role. Practice explaining complex validation processes in simple terms. You might be asked to present a scenario or a past project, so being clear and concise will help you stand out.
✨Be Ready for Team Dynamics
This position requires both independent work and teamwork. Think of examples where you’ve successfully collaborated with others or led a project. Highlighting your proactive attitude and ability to adapt will resonate well with the interviewers.
