At a Glance
- Tasks: Lead validation activities and ensure compliance in a cutting-edge cell therapy environment.
- Company: Join RoslinCT, a leader in life-changing therapies with a collaborative culture.
- Benefits: Generous salary, 31 days leave, private healthcare, and flexible benefits.
- Why this job: Make a real impact in the field of gene therapy while developing your career.
- Qualifications: Degree in Life Sciences or equivalent experience in a GMP environment.
- Other info: Inclusive workplace that values diversity and supports your career growth.
The predicted salary is between 40000 - 50000 £ per year.
Location: Shawfair
Who are we? We are RoslinCT, a world‑leading cell and gene therapy contract development and manufacturing organisation creating cutting‑edge therapies that change people’s lives. Collaborative, dedicated and talented people are the backbone of our culture, working both autonomously and in driven teams to make life‑changing products utilising ground‑breaking science.
Why join us? The opportunity to join a rapidly expanding company which is changing lives, giving you the skills and experience to develop your career. A generous salary package – we reward our people at the level they deserve. 31 days of annual leave, plus 4 public holidays which increases with tenure. A competitive company pension scheme to help you save for the future. Group Life Cover – you are automatically covered for three times your basic salary to give you and your family peace of mind. Private healthcare and access to mental health/wellbeing support as your health and wellbeing means a lot to us. Flexible benefits such as retail discounts and access to the Cycle2Work scheme.
Your new role: An exciting opportunity for a Senior Validation Officer to join our Validation team. You’ll be responsible for planning, managing and executing RoslinCT validation activities to include facility and equipment validation, qualification and re‑verification. Prepare and implement validation protocols and reports. Perform and manage routine qualification, calibration and maintenance of equipment when required. Complete and review quality related documentation, including validation documents in accordance with GMP and standard operating procedures. Lead on the validation of new equipment and provide guidance and assistance to team members as needed. Communicate procedures and results with clients, and ensure patient and client information is kept confidential at all times.
About you: Proven experience working with a validation program in a GMP environment. Experience working in a sterile manufacturing facility. Flexible and adaptable, with the ability to respond effectively to shifting project priorities. Excellent communication skills, particularly engaging with customers and service providers. Proficient in IT, specifically with Microsoft Word & Excel. Ideally, you will have experience with cleanroom facilities, manufacturing and QC testing equipment. Additionally, a working knowledge of UK laws and regulations relating to cell therapy products and tissue donation would be advantageous.
Qualifications: A degree in a Life Sciences or related subject. We will also consider candidates with equivalent training and experience.
Next Steps: If this sounds like you, then please hit ‘Apply’ now. We will ask you to upload your CV and complete a short application form detailing why you are interested and why we should hire you. At RoslinCT, we’re all about inclusivity and creating a fair, welcoming workplace. Our goal is to make sure everyone knows they’re valued and encouraged to be themselves, whether they’re our employees, customers, or partners. We take pride in being an equal opportunity employer. We treat all applicants fairly and don’t discriminate based on any protected characteristics. So, no matter who you are, we welcome your application with open arms. If you’ve got any specific needs or concerns regarding accessibility during the recruitment process, don’t hesitate to reach out to us. We’re here to assist and make things as smooth as possible for you.
Senior Validation Officer in Danderhall employer: RoslinCT
Contact Detail:
RoslinCT Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior Validation Officer in Danderhall
✨Tip Number 1
Network like a pro! Reach out to people in the industry, attend events, and connect on LinkedIn. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by researching RoslinCT and understanding their mission. Tailor your answers to show how your experience aligns with their goals. We want to see your passion for cell and gene therapy!
✨Tip Number 3
Practice makes perfect! Do mock interviews with friends or use online resources to get comfortable with common questions. The more you practice, the more confident you'll feel when it’s time to shine.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets seen. Plus, we love seeing candidates who take that extra step to engage with us directly.
We think you need these skills to ace Senior Validation Officer in Danderhall
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior Validation Officer role. Highlight your experience in validation programs and GMP environments, as well as any relevant qualifications. We want to see how your skills match what we're looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you're passionate about joining RoslinCT and how your background makes you a great fit for our team. Keep it engaging and personal – we love to see your personality come through!
Showcase Your Communication Skills: Since excellent communication is key for this role, make sure to demonstrate your ability to engage with clients and team members in your application. Whether it's through your CV or cover letter, let us know how you effectively communicate complex information.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the easiest way for us to receive your application and ensures you don’t miss out on any important updates. Plus, it shows us you’re keen to join our amazing team!
How to prepare for a job interview at RoslinCT
✨Know Your Validation Stuff
Make sure you brush up on your knowledge of validation processes, especially in a GMP environment. Be ready to discuss your previous experiences with facility and equipment validation, as well as any specific protocols you've implemented.
✨Show Off Your Communication Skills
Since you'll be engaging with clients and team members, practice articulating complex ideas clearly and concisely. Prepare examples of how you've effectively communicated procedures and results in past roles.
✨Be Ready for Flexibility
RoslinCT values adaptability, so think of instances where you've successfully managed shifting project priorities. Highlight your ability to stay calm under pressure and adjust your plans as needed.
✨Familiarise Yourself with Regulations
Brush up on UK laws and regulations related to cell therapy products and tissue donation. Being knowledgeable about these topics will show that you're serious about compliance and patient safety, which is crucial in this role.