At a Glance
- Tasks: Support validation activities by generating and revising essential documentation.
- Company: Join a leading pharmaceutical company focused on compliance and innovation.
- Benefits: Competitive salary, health benefits, and opportunities for professional growth.
- Other info: Collaborative work environment with a focus on career development.
- Why this job: Make a real impact in the pharmaceutical industry while ensuring safety and compliance.
- Qualifications: Experience in technical documentation and knowledge of pharmaceutical regulations required.
The predicted salary is between 35000 - 45000 € per year.
To support validation activities at the Pirbright Site, the Validation Execution Specialist will generate and/or revise validation documentation for utilities, facilities, processes, and equipment, ensuring delivery of commitments in line with timelines and internal/external validation regulations.
Tasks include:
- Experience authoring technical documentation.
- In-depth knowledge of the regulated pharmaceutical industry and compliance expectations (VMD, FDA, Eudralex Annex 1).
- Good understanding of industry guidelines (ISPE, PDA, ISO, HTM).
- Good understanding of GxP water systems, HVAC systems, pharmaceutical gases, etc.
- Experience in Biologicals beneficial.
- Experience in Sterile Manufacturing beneficial.
- Ability to work collaboratively across functions.
A Disclosure and Barring Service (DBS) check will be required for the successful candidate. Any offer of employment will be subject to satisfactory DBS certificate.
Validation Execution Specialist in Surrey employer: Boehringer Ingelheim GmbH
At our Pirbright Site, we pride ourselves on being an exceptional employer that fosters a collaborative and innovative work culture. As a Validation Execution Specialist, you will benefit from comprehensive employee growth opportunities, competitive remuneration, and a commitment to compliance and quality in the regulated pharmaceutical industry. Join us to be part of a team that values your expertise and supports your professional development in a dynamic environment.
StudySmarter Expert Advice🤫
We think this is how you could land Validation Execution Specialist in Surrey
✨Tip Number 1
Network like a pro! Reach out to folks in the pharmaceutical industry, especially those who know about validation processes. A friendly chat can lead to insider info on job openings that might not even be advertised yet.
✨Tip Number 2
Show off your skills! When you get the chance to meet potential employers, whether at a job fair or an informal coffee chat, bring along examples of your technical documentation. It’s a great way to demonstrate your expertise in validation activities.
✨Tip Number 3
Stay updated on industry regulations! Make sure you’re familiar with the latest compliance expectations from VMD, FDA, and Eudralex Annex 1. This knowledge will not only boost your confidence but also impress interviewers.
✨Tip Number 4
Apply through our website! We’ve got loads of opportunities waiting for you, and applying directly helps us see your application faster. Plus, it shows you’re keen on joining our team!
We think you need these skills to ace Validation Execution Specialist in Surrey
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the Validation Execution Specialist role. Highlight your experience with technical documentation and any relevant knowledge of the pharmaceutical industry. We want to see how your skills align with our needs!
Showcase Your Compliance Knowledge:Since compliance is key in this role, don’t forget to mention your understanding of regulations like VMD, FDA, and Eudralex Annex 1. We’re looking for someone who knows their stuff, so let us know how you meet these expectations!
Highlight Collaborative Experience:This role requires working across functions, so share examples of how you've successfully collaborated in the past. We love teamwork, and showing us your ability to work well with others will definitely make your application stand out!
Apply Through Our Website:We encourage you to apply through our website for a smoother process. It’s the best way for us to receive your application and ensures you don’t miss any important updates from us. Let’s get started on this journey together!
How to prepare for a job interview at Boehringer Ingelheim GmbH
✨Know Your Regulations
Make sure you brush up on the key regulations like VMD, FDA, and Eudralex Annex 1. Being able to discuss these confidently will show that you understand the compliance expectations in the pharmaceutical industry.
✨Showcase Your Technical Writing Skills
Since the role involves authoring technical documentation, prepare examples of your previous work. Bring along samples or be ready to discuss how you've generated or revised validation documents in the past.
✨Understand GxP Systems
Familiarise yourself with GxP water systems, HVAC systems, and pharmaceutical gases. Be prepared to explain how these systems work and their importance in validation processes during the interview.
✨Collaborative Mindset
This role requires working across functions, so think of examples where you've successfully collaborated with others. Highlight your teamwork skills and how you can contribute to a positive working environment.
