Test Labs cut through the complexity of medical device testing, their set up allows them to offer highly tailored solutions globally, ensuring strict compliance with EU CE Mark, UKCA Mark, FDA, Health Canada and SFDA requirements. Our core values:
Hungry, Humble, Smart
serve as the core foundations of our organisational culture, driving us toward unprecedented achievements in Healthcare Innovation, enabling us to deliver Better Healthcare, Faster.
We are relentless in our pursuit of excellence. We hunger for knowledge, challenges, and the constant evolution of healthcare solutions, which drives us to push boundaries, fostering a dynamic, innovative environment. Grounded in humility, we recognise the collective strength of our diverse team. We acknowledge that collaboration fuels innovation. Our humility allows us to learn from each other, embrace feedback, and continuously grow, fostering a culture of mutual respect and open communication. Intelligence is not just about technical prowess; it's about emotional intelligence, effective collaboration, and strategic thinking.
Together, these values create a culture where ambition meets collaboration, where passion meets practicality, and where innovation meets impact. People who live our values, thrive at Test Labs and benefit both personally and professionally by engaging in the Test Labs journey.
What are we looking for in this position?
Act as the Technical Lead, managing studies and complying to ISO17025 requirements
Be fully responsible for ISO17025 studies for GLP and non GLP studies, complying to all regulations
Conduct Medical Device testing where required
Develop new test methods that when applied support new claims and demonstrate compliance with regulatory/quality standards
Work along side the sales and marketing team to act as the technical expert when supporting client needs and questions
Train new staff and take on responsibility of continuous improvement and training schedule
Lead, engage and develop a tram of Laboratory analyses with 1-2-1's, daily huddles and reporting routines
Create and schedule weekly team rota's and assign studies to relevant analysts/scientists
Ensure all routine checks and calibrations are performed in line with the requirements and are compliant to the QMS
To be part of any customer meeting and contribute positively with technical advice and being able to fully participate in Outline Study Plan creation followed by proposals where necessary
Adherence to the company Management Systems and external certifications/accreditations maintained including responsibilities outlined in the company policies and procedures such as the Overview and context of the organisation
What will we need you to have?
Always represent our Core Values: Hungry, Humble, Smart
Ability to maintain a high level of attention to detail and a methodical approach
Excellent verbal and written communication skills
Ability to work in, and adapt to, a rapidly changing environment
Ability to work cooperatively with other to complete tasks and implement process improvement
Ability to prioritise and manage workload within a fast-paced environment
The ability to troubleshoot problems and develop solutions
Experience working in a GLP and UKAS accredited laboratory
Experience in managing a team of analysts
At least 3 years of experience working in a laboratory
What will you get?
33,000 to 38,000 per annum, depending on experience
Profit Sharing Bonus Scheme
Commitment to your Personal & Professional Development
Contributory Pension
* Employee Discounts and Employee Assistance Platform
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