Be part of something altogether life-changing!
Working at Cytiva 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.
Forming part of the Biotechnology segment at Danaher, we bring together dedicated technical expertise and talent to develop the next generation of life-changing therapeutics.
The Senior Manager QA for Custom Engineering & SCO (Standard and Custom Operations) Sweden, independently leads, coordinates and prioritizes the work within the assigned site/s to ensure successful management of the QMS and associates processes.
The role is responsible for ensuring that the Custom Engineering Sweden team executes on deliveries, internal audits, QMS training, QMS documentation, complaints, NC/CAPA, product holds and field actions. Ensures compliance of the processes and drives a strong Quality Culture by engagement, empowerment, and inclusiveness.
This position is part of the QA Custom Hardware department located in Uppsala, Sweden and will be onsite. At Cytiva, our vision is, to advance future therapeutics from discovery to delivery.

What you will do:
Be responsible for engaging strong intra departmental and cross-functional/organizational relationships to drive compliance and ensuring product quality.
Be the QA representative in project steering committees as agreed with QA Director.
Lead, coordinate, prioritize and follow-up the work within the team.
Engage, coach and develop the personnel.
Set goals for the team and follow up on completion.
Drive internal improvement work to assure continuous improvements.
Support key quality activities and be open to take on additional tasks supporting the overall performance of the QA Department.

Who you are:
Bachelor’s degree preferably in a science or engineering discipline.
A minimum of 5 years of experience in the Quality Assurance field.
Experience of working as a manager within Quality Assurance/Quality Control
Comprehensive understanding of ISO 9001 requirements.
Experienced in continuous improvement methodologies & tools.
Experienced in leading external audits, including customer communications.
Excellent organizational, presentation, meeting facilitation and technical writing skills.

It would be a plus if you also possess previous experience in:
Knowledge and awareness of the methods and techniques of Quality Control in the manufacturing industry.
Technical knowledge of systems/devices used in the biopharma field.
Fluency in Swedish both written and verbal communication.