Regulatory Affairs Senior Specialist

Bring more to life.     Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?      At   Cepheid ,   one of   Danaher’s   15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.       You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And   by harnessing   Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.     At Cepheid, we are passionate about improving health care through fast, accurate, molecular diagnostic systems and tests. As a member of our team, you’ll get to make an immediate, measurable impact on a global scale, within an environment that fosters career growth and development. Our mission drives us to develop groundbreaking solutions for the world’s most complex health challenges. Together, we bring MORE change to the world.   Learn about the   Danaher Business Syste m   which makes everything possible.   The   QRC On-market Sustainment team   creates the regulatory strategy and assessments for complex post market design changes; interfaces with global regulatory authorities including BSI and WHO; and collaborates cross functionally to assess regulatory risk, define data and submission requirements as a result of design changes.   As the  Regulatory Affairs  Senior   Specialist   is responsible for s upporting global regulatory activities for Cepheid's in vitro diagnostic products throughout the product lifecycle. This role drives regulatory compliance by leading regulatory assessments, preparing and   maintaining   technical documentation, managing regulatory submissions, and supporting interactions with global regulatory authorities and Notified Bodies. The position plays a key role in enabling product registrations, implementation of product changes, and continued market access globally.    This position reports to the Principal Regulatory Affairs Specialist and is part of the Regulatory Affairs organization,   located   in Solna, Stockholm, Sweden, and will be an on-site role.    In this role, you will have the opportunity to:   Serve as the RA   Lead   on Project teams and provide   highly complex   regulatory impact assessments for analytical, manufacturing, labeling, packaging, and supplier changes to ensure global compliance.    Prepare, compile,   submit , and   maintain   regulatory submissions and technical documentation for global markets, including EU IVDR and international regulatory pathways.    Manage regulatory change control activities and interactions with Notified Bodies and regulatory authorities.    Serve as a key regulatory business partner to manufacturing, operations, supply chain, RA NPD,   Global Product Management   and the Commercial QRA Center of Excellence to define data requirements,   support product lifecycle management, continuous improvement initiatives, and regulatory compliance strategies   through use of DBS tools .   Monitor emerging regulatory requirements, provide regulatory intelligence, and deliver regulatory guidance and training across the organizatio n ;   act as regulatory affairs l ead for compliance during internal and external audits, post market surveillance, nonconformances, CAPAs and complaint invest igations.   The essential requirements of the job include:   Bachelor’s degree or higher in Life Sciences, Biotechnology, Biomedical Sciences, Chemistry, Regulatory Affairs, Engineering, or a related scientific discipline Several years  of experience in Regulatory Affairs, Quality Assurance, or   a related   regulated function within the IVD, medical device, biotechnology, or life sciences industry.   Experience preparing and   maintaining   technical documentation and regulatory submissions supporting EU IVDR, IVDD, MDR, FDA, or other global regulatory