1 Validation Specialist Job in Edinburgh, IN
RoslinCT is Hiring a Validation Specialist Near Edinburgh, IN
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.
Find out more about what we do here!
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.
- An exciting opportunity to join our high performing team as a Validation Specialist.
- Responsible for the regulatory compliance of the facility and equipment validation activities and the preparation and execution of validation protocols and reports.
- You will also support GMP project management activities in the validation of a new cell therapy facility.
- Manage and perform routine qualification, calibration, and maintenance of equipment.
- Complete and review quality related documentation including but not limited to validation documents, change controls, deviations, and risk assessments in accordance with GMP and standard operating procedures.
- Ensure that the confidentiality of all information to clients and patients is always maintained.
- You may communicate procedures and results with clients.
- Plan and undertake the validation of new equipment and to advise and assist others in this.
- Comply with Health and Safety policies and procedures.
- Provide out of hours cover for critical equipment alarms as required on a rotational basis.
- Contribute to the set up and execution of the validation schedule for the new facility.
- Ensure the data integrity of software systems.
- Experience with cleanroom facilities, manufacturing, and QC testing equipment would be advantageous.
- Demonstrable experience of working with a validation programme in a GMP environment.
- Experience in a sterile manufacturing facility strong preferred.
- Flexible and adaptable to react to rapid changes in project priorities.
- A working knowledge of UK laws and regulations for cell therapy products and tissue donation would be advantageous.
- Excellent communication and interpersonal skills, with the ability to build strong working relationships internally and externally
- Competent in the use of Microsoft Office products
- Exceptional organisational and planning skills with the ability to multi-task in a fast-paced environment
- Excellent attention to detail with a real desire to continually develop and improve our processes.
- A BSc in a Life Science subject or other equivalent experience.
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 at jobs@roslinct.com. We’re here to assist and make things as smooth as possible for you.
Job Summary
Full Time
$52k-70k (estimate)
07/04/2024
08/01/2024
The job skills required for Validation Specialist include Planning, Project Management, Validation Protocols, Calibration, Microsoft Office, Change Control, etc. Having related job skills and expertise will give you an advantage when applying to be a Validation Specialist. That makes you unique and can impact how much salary you can get paid. Below are job openings related to skills required by Validation Specialist. Select any job title you are interested in and start to search job requirements.
The following is the career advancement route for Validation Specialist positions, which can be used as a reference in future career path planning. As a Validation Specialist, it can be promoted into senior positions as a Validation Engineer II that are expected to handle more key tasks, people in this role will get a higher salary paid than an ordinary Validation Specialist. You can explore the career advancement for a Validation Specialist below and select your interested title to get hiring information.
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