Associate Director, Quality Assurance SupportCSL Behring • Bern, Berne, Switzerland

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Associate Director, Quality Assurance Support

CSL Behring

Bern, Berne, Switzerland

Bern, Berne, Switzerland

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About

CSL Behring is a global biotherapeutics leader driven by its promise to save lives. In Bern, more than 1500 employees develop and deliver life-saving therapies to treat people with rare and serious medical conditions worldwide. For our location in Bern, we are currently looking for a Associate Director, Quality Assurance Support Responsibilities Responsible for routine and non-routine quality oversight activities in collaboration with local operational units (Maintenance & Utilities, Quality Control, warehouse & internal transport) and qualification activities in Opex and periodic re-qualification projects Ensures operational quality management according to cGMP to guarantee appropriate service quality for Value Streams and compliance with CSL standards and procedures Reviews and approves complex GxP records and documentation Supports and approves complex quality risk assessments, non-conformances, investigations, CAPAs, and change controls Monitors relevant quality performance metrics and drives improvement initiatives Leads project management and implementation of complex cross-functional and global projects Acts as Subject Matter Expert (SME) for complex deviations and changes during inspections and audits; collaborates with global QA Support Functions Quality Oversight & Stakeholder Collaboration Ensures proactive QA oversight and drives quality decisions with stakeholders across maintenance/utilities, utility monitoring, material management, warehousing, and QC Conducts periodic warehouse floor tours with warehouse supervision and Supply Chain teams to address improvements, exceptions, and material usage decisions Initiates and supports implementation of new “Quality on the Floor” activities Deviation, Change & Document Handling Independently manages complex and cross-functional deviations at local and cross-site level Performs “Quality Delegate” function for change management Reviews and provides QA approval for GxP documentation within assigned areas Additional Responsibilities Reviews and completes APR/PQR raw material data Leads cross-functional Tier 1 meetings (QC, warehouse, M2U) Coordinates and delivers GMP training and qualification of new employees in QA Support Functions Independently prepares and presents quality investigations and changes to health authorities Qualification 8 years of experience in a similar role with a high degree of independence and strong self-directed learning capabilities cGMP and Compliance Engineering & maintenance operations Utility monitoring programs Material management, warehousing & logistics Quality control & analytical methods Change control management Deviation management CAPA management Strong collaboration skills with proven ability to build cross-functional networks and drive efficient interfaces between departments Coaching & mentoring skills with the ability to upskill colleagues in areas of expertise Excellent communication abilities , capable of explaining complex technical matters in a clear, concise and precise manner Strong influencing and presentation skills , enabling effective stakeholder engagement and decision-making We are looking forward to receiving your online application. Applications must include a motivation letter and CV, as well as letters of references and copies of relevant transcripts and/or diplomas in the original language. Please include all these in one document together with the CV. About CSL Plasma CSL Plasma operates one of the world’s largest and most sophisticated plasma collection networks, with over 350 plasma collection centers in the U.S., Europe and China. Headquartered in Boca Raton, Florida, CSL Plasma is a subsidiary of CSL Behring, a global biotherapeutics business and a member of CSL. Plasma collected at CSL Plasma facilities is used by CSL Behring for the sole purpose of manufacturing lifesaving plasma-derived therapies for people in more than 100 countries. The parent company, CSL, headquartered in Melbourne, Australia, employs 32,000 people. Learn more about CSL Plasma here https://www.cslplasma.com/ and CSL, CSL Behring, CSL Seqirus and CSL Vifor here https://www.csl.com/ . Learn more about CSL, CSL Behring, CSL Seqirus and CSL Vifor here at https://www.csl.com/ and CSL Plasma at https://www.cslplasma.com/ . Our Benefits For more information on CSL Plasma benefits visit https://cslbenefits.com/cslp . You Belong at CSL At CSL, Inclusion and Belonging is at the core of our mission and who we are. It fuels our innovation day in and day out. By celebrating our differences and creating a culture of curiosity and empathy, we are able to better understand and connect with our patients and donors, foster strong relationships with our stakeholders, and sustain a diverse workforce that will move our company and industry into the future. To learn more visit https://www.csl.com/careers/inclusion-and-belonging Equal Opportunity Employer CSL is an Equal Opportunity Employer. If you are an individual with a disability and need a reasonable accommodation for any part of the application process, please visit https://www.csl.com/accessibility-statement .

Bern, Berne, Switzerland

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