OBS! Ansökningsperioden för denna annonsen har
passerat.
Arbetsbeskrivning
Be part of something altogether life-changing!
Working at Cytiva in the Life Sciences industry means being at the forefront of providing new solutions to transform human health. Our incredible customers undertake life-saving activities ranging from fundamental biological research to developing innovative vaccines, new medicines, and cell and gene therapies.
At Cytiva you will be able to continuously improve yourself and us – working on challenges that truly matter with people that care for each other, our customers, and their patients. With associates across 40 countries, Cytiva is a place where every day is a learning opportunity – so you can grow your career and expand your skills in the long term. Your health and wellbeing are important to us and together we will not compromise on safety in the workplace or the environment.
Cytiva is proud to work alongside a community of nine fellow Danaher Life Sciences companies. Together, we’re pioneering the future of science and medicine, developing products that enable researchers in the fight to save lives.
Our QA department is growing and we are now looking for a new colleague to one of our QA teams at Cytiva in Uppsala. The team consists of around 8 persons and is responsible for internal audits, customer audits, deviations, complaints, CAPA management, documentation management and QMS training. You will be working closely with experienced colleagues where team spirit, flexibility and support are important factors.
We are looking for a person who has a strategic mind set, is analytical and structured and with good communication and collaborative skills.
What you'll do:
Accountable for managing the QMS training plan for the site.
Monitoring and trending training KPIs and drive improvements based on performance.
Ensure process efficiency and compliance effectiveness.
Participate in global forum as the QMS Training Lead.
Provide a structured QMS onboarding program and maintain a solid foundation and knowledge of the QMS processes and the quality culture.
Assign new QMS trainings to associates within the training system.
Review documents within the QMS training Plan.
Act as business admin and support in the Cytiva Learning System.
Collaborate with relevant stakeholders to identify and implement training and development opportunities continuously.
Develop relevant QMS training based on internal and external feedback.
Improve the QMS training process.
Drive opportunities to leverage best practices across the site.
Lead trainers and coordinators in delivering the training content and meeting the site QMS training objectives.
Who you are
Bachelor's / Master’s degree from university.
Experience in training, development, or facilitation.
Experience from the life science industry or regulatory industry (meritorious).
Able to work in a matrix environment with multiple stakeholders and to develop strong relationships with key stakeholders.
Solid influencing skills.
Ability to plan and manage a range of priorities, and deliver projects to deadline, within an agreed/defined standard.
Ability to identify new and creative solutions to business challenges.
Ability to communicate effectively in both Swedish and English (written and oral).
We are applying a hybrid working model with the possibility to work partly from home. Our business is growing quickly, and we hire across the board. Selections, interviews and recruitment take place on an ongoing basis.