Stockholm Group Expert QCIO

Job description

Become part of a vital chain and contribute to our common goal of making people’s lives better. Octapharma is one of the largest human protein manufacturers in the world, developing and producing medicines sourced from human plasma and human cell lines. We are a privately-owned company, where the warmth of family meets the scale of a global organisation. As Group Expert QCIO , you will play a key role representing cQC in new pipeline products, the optimization of licensed products, and technology transferanalytical projects and continuous improvements across our global Quality Control organisation. Working closely with stakeholders from QC, R&D and Method Validation, you will coordinate critical analytical activities and ensure successful collaboration across functions and sites. This position is ideal for someone with a strong analytical background who enjoys leading projects, building relationships and bringing people together to achieve common goals. Octapharma AB is located in northwestern Kungsholmen in Stockholm and has approximately 1,100 employees. This is a temporary position covering a parental leave, with an expected duration of approximately one year. The position is based in Stockholm, with a preferred start date as soon as possible or as agreed. Join us in shaping our vision to provide new health solutions advancing human life. Your main tasks and responsibilities Drive and coordinate innovation and improvement projects within Corporate Quality Control Act as the key link between project teams, analytical experts, Corporate QC Method Validation and local QC organisations Coordinate and follow up analytical method development, validation and transfer activities across development and technology transfer projects Represent Corporate QC in cross-functional project teams and provide quality control expertise Prepare and present analytical method status assessments, analytical risk assessments and project updates to stakeholders Drive GMP-related activities including risk assessments, change controls, SOPs and other quality documentation Your expertise and ideal skill set M.Sc. or Ph.D. in Chemistry, Biochemistry, Analytical Chemistry or a related scientific discipline Experience of analytical methods and method validation within a GMP-regulated environment Strong communication and stakeholder management skills with the ability to build effective collaborations across functions and sites Experience of coordinating projects and driving activities to completion Ability to work independently and navigate a global organisation with multiple stakeholders Fluency in English Additional language skills in French, German, or Swedish are considered an advantage. Your department - where you make an impact Group Innovation for QC Operations collaborates closely with other departments to support the development of new pipeline products, the optimization of licensed products, and technology transfers. The team combines project leadership and analytical expertise to support product development, product lifecycle activities and technology transfers Working closely with stakeholders across functions and sites, the department contributes to the continuous development of Octapharma's global Quality Control organisation "What I appreciate most about leading this team is the combination of a collaborative atmosphere and the opportunity to make a real impact across our global organisation. Although we are a relatively small team, we work closely with colleagues, experts and stakeholders across multiple sites and functions. As Group Project Manager QCIO, you will play a key role in supporting Octapharma’s analytical development, validation and technology transfer activities, helping ensure that our global Quality Control organisation can meet both current and future business needs. If you enjoy bringing people together, driving projects forward and building strong collaborations, this is a fantastic opportunity to make a difference." Barbara Malkowsky, Group Head of QC Method Validation and Analytical Lifecycle Thrive with us Company restaurant & meal subsidy Training & further education Health promotion Parking spaces and good public transport connections Company and team events Enjoy these attractive benefits! You can find all offers here: Benefits It´s in our blood We live diversity and stand for equal opportunities as an employer! We therefore look forward to receiving your application - regardless of age, gender, origin, sexual orientation, and religion. Apply Today! Please apply in English. If you have questions about the position, contact Josefina Kihlström (Responsible recruiter) at josefina.kihlstrom@octapharma.com. The application deadline Is 2026-11-17, but the position may be filled before then. Want to find out more about us? Visit our website Octapharma Career and follow us daily on LinkedIn ! About Octapharma Octapharma is one of the largest human protein manufacturers in the world, developing and producing human proteins from human plasma and human cell lines. We employ more than 11,000 people worldwide to support the treatment of patients in 120 countries with products across three therapeutic areas: Immunotherapy, Haematology and Critical Care. With seven R&D sites and five state-of-the-art manufacturing facilities in Austria, France, Germany, and Sweden, Octapharma also operates over 195 plasma donation centres across Europe and the US. With four decades of experience, we are committed to advancing patient care worldwide. About Octapharma Octapharma is one of the largest human protein manufacturers in the world, developing and producing human proteins from human plasma and human cell lines. We employ more than 11,000 people worldwide to support the treatment of patients in 120 countries with products across three therapeutic areas: Immunotherapy, Haematology and Critical Care. With seven R&D sites and five state-of-the-art manufacturing facilities in Austria, France, Germany, and Sweden, Octapharma also operates over 200 plasma donation centres across Europe and the US. With four decades of experience, we are committed to advancing patient care worldwide. Apply now » Find similar jobs: Global Website Data Privacy Statement Cookie Consent Manager Legal Statement Opens in a new tab. Opens in a new tab. © 2026 Octapharma AG Cookie Consent Manager When you visit any website, it may store or retrieve information on your browser, mostly in the form of cookies. 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