At a Glance
- Tasks: Lead validation activities and ensure compliance in a dynamic quality department.
- Company: Join a forward-thinking company dedicated to sustainability and innovation.
- Benefits: Empowerment, recognition, growth opportunities, and a supportive team environment.
- Other info: Inclusive workplace welcoming diverse backgrounds and experiences.
- Why this job: Make a real impact on product quality and contribute to a sustainable future.
- Qualifications: Degree in science or engineering with 5+ years in cGMP validation.
The predicted salary is between 60000 - 80000 £ per year.
Your key responsibilities:
- Leadership role within the Quality Department responsible for the management and co-ordination of the site cGMP validation activities.
- Support validation activity during design, installation & commissioning of new equipment, processes, packaging lines & facilities and utilities.
- Ensure the validated status of site facilities, i.e., equipment, processes, CSV and utilities is complete and compliant with internal local and corporate procedures, relevant regulatory requirements and industry guidance.
- Authoring, reviewing, executing and maintaining validation documentation including site Validation Master Plan and Site Validation Strategy.
- Support Production departments in validation activities for processes and equipment.
- Preparation and management of validation plans, protocols and reports.
- Support and coordinate with corporate validation team.
- Supporting external audits including customer and regulatory inspections, presenting and explaining relevant validation information to inspectors/auditors.
- Execute validation protocols and drive to completion any CAPA associated with non-conformances raised.
- Use quality risk management tools (e.g., FMEA, System Impact Assessments) to ensure that risks are appropriately identified, documented and managed.
- Ensure product quality through robust testing and process monitoring including the use of statistical techniques.
- Support Cleaning, Utilities and Computer System Validation.
We offer:
- Empowerment to make meaningful contributions while upholding ethical standards.
- Recognition and celebration of your efforts and accomplishments.
- Being a part of an agile local team at the site.
- Opportunities for growth and advancement for those who embrace innovation and take initiative.
- Opportunity to build a career in a company supplying sustainable products.
- Dedication to creating better futures for customers, communities, people, and the planet.
- Responsibility and accountability in living company values and driving sustainable solutions.
- Supportive environment where individuals are empowered to progress and contribute to meaningful change.
You bring:
- Successful candidates should have a degree in a relevant science or engineering discipline.
- Minimum 5 years of validation and qualification experience in a cGMP regulated life science industry, i.e., Pharmaceutical, API or Bio-tech.
- Other essential behaviors are excellent communication and organizational skills, and the ability to work independently & within cross functional teams.
We’re proud to be an equal opportunity employer, and we’re serious about making our hiring process as fair and inclusive as possible. We welcome candidates from all backgrounds — no matter your gender, ethnicity, sexual orientation, or anything else that makes you, you. And if you have a disability or need any support through the application process, we’re here to help.
Lead Expert Validation, Dalry employer: dsm-firmenich
As a Lead Expert Validation at our Dalry site, you will join a dynamic and supportive team dedicated to upholding the highest standards of quality in the life sciences industry. We offer a culture that celebrates innovation and empowers employees to make meaningful contributions, alongside opportunities for professional growth and advancement. With a commitment to sustainability and ethical practices, you will be part of a company that values your efforts and fosters a collaborative environment where every voice is heard.
StudySmarter Expert Advice🤫
We think this is how you could land Lead Expert Validation, Dalry
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, attend relevant events, and engage with professionals on platforms like LinkedIn. We all know that sometimes it’s not just what you know, but who you know that can help you land that dream job.
✨Tip Number 2
Prepare for interviews by researching the company and its culture. Understand their values and how they align with yours. We want you to shine, so practice common interview questions and think about how your experience in validation can add value to their team.
✨Tip Number 3
Showcase your skills through real-life examples. When discussing your experience, focus on specific projects or challenges you've tackled in validation. We love hearing about how you’ve made an impact, so don’t hold back!
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, we’re always looking for passionate individuals who are ready to make a difference in the validation space.
We think you need these skills to ace Lead Expert Validation, Dalry
Some tips for your application 🫡
Tailor Your CV:Make sure your CV reflects the skills and experiences that match the Lead Expert Validation role. Highlight your cGMP validation experience and any leadership roles you've held. We want to see how you can contribute to our Quality Department!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to explain why you're passionate about validation in the life sciences industry and how your background aligns with our values at StudySmarter. Keep it engaging and personal!
Showcase Your Achievements:Don’t just list your responsibilities; showcase your achievements! Use specific examples of how you've improved processes or led successful validation projects. We love seeing how you’ve made a difference in your previous roles.
Apply Through Our Website:We encourage you to apply directly through our website for the best chance of getting noticed. It’s super easy, and you’ll be able to keep track of your application status. Plus, we love seeing candidates who take the initiative!
How to prepare for a job interview at dsm-firmenich
✨Know Your Validation Stuff
Make sure you brush up on your cGMP validation knowledge. Understand the key processes, equipment, and regulatory requirements that are relevant to the role. Being able to discuss specific examples from your past experience will show that you’re not just familiar with the theory but have practical insights too.
✨Showcase Your Leadership Skills
Since this is a leadership role, be prepared to talk about your experience managing teams and coordinating projects. Think of specific instances where you led a successful validation project or resolved conflicts within a team. This will demonstrate your ability to lead effectively in a quality department.
✨Prepare for Technical Questions
Expect some technical questions related to validation protocols, risk management tools like FMEA, and how you handle non-conformances. Practise articulating your thought process clearly and confidently, as this will reflect your expertise and problem-solving skills.
✨Emphasise Communication and Collaboration
Highlight your communication skills and your ability to work within cross-functional teams. Be ready to share examples of how you’ve successfully collaborated with production departments or supported audits. This will show that you can effectively bridge gaps between different teams and ensure compliance.
