QA Analytical Specialist at Sobi

Basel, Basel-City, Switzerland -

Full Time

Start Date

Immediate

Expiry Date

22 Jul, 26

Salary

0.0

Posted On

23 Apr, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

GMP compliance, Analytical method validation, Stability studies, Deviation management, CAPA, Change control, Quality assurance, Analytical chemistry, Bioassays, Regulatory affairs, Technical agreements, SOP development, Quality evaluation, Cross-functional collaboration, Pharmaceutical quality systems

Industry

Pharmaceutical Manufacturing

Description

Company Description Statistics show that women and underrepresented groups tend to apply to jobs only if they meet 100% of the qualifications. Sobi encourages you to change that statistic and apply. Rarely do candidates meet 100% of the qualifications. We look forward to your application! At Sobi, the work we do every day redefines the standards of care and transform the lives of people living with rare diseases. As a diverse team of entrepreneurial people, we are passionate about our growth journey towards becoming a global leader, making a difference for rare disease patients, moving quickly and always challenging the status quo. We are committed to an inclusive, sustainable and flexible workplace that fosters growth and development. Job Description About the role Global Quality plays a key role in making sure our medicines meet internal standards, regulatory expectations, and the commitments in our registration files. As an independent quality organisation, we bring the expertise to deliver on these commitments—while continuously strengthening our capabilities, developing our people, and evolving our quality system to support the business as we grow. As QA Analytical Specialist, you’ll be the quality partner for analytical activities and stability studies for products where Sobi is the MAH. You’ll ensure GMP-compliant methods and data support reliable release and stability testing for both clinical and commercial supply—working closely with internal stakeholders and external partners to keep quality, compliance, and patient impact at the centre of everything we do. It is a Hybrid role and can be based in either Stockholm or Basel, reporting to Head of Quality Product Lifecycle & Clinical Supply. Key Responsibilities Coordinator and Quality approver for deviations, CAPA and change controls. QA-approver for GMP-related analytical activities, e.g. validation and technology transfer of analytical methods used for in-process control, release and stability studies. Performance of quality evaluation of CLOs. QA contact for CLOs Provide Quality Assurance for stability studies for products where Sobi is the MAH, including approving plans and protocols. Perform QA review and approval of extension of expiry date of critical analytical material, including but not limited to reference standards and control samples. Perform QA review and approval of product specifications. Give support to Global Regulatory Affairs / CMC in analytical quality issues for variations and market expansions. Act as a representative of Global Quality and provide QA analytical guidance to support projects in order to ensure compliance with GMP Manage Quality Technical Agreements with CLOs. Author, review and approve SOPs and related documentation related to the position. Qualifications About you You’re a quality-minded analytical professional who enjoys working cross-functionally, taking ownership, and bringing structure to complex scientific work. You combine strong GMP understanding with a collaborative mindset, and you’re motivated by the opportunity to help deliver reliable, high-quality medicines to patients who need them most. Qualifications University degree in Chemistry, Biology, Biotechnology, Pharmaceutical Science, or similar. 5+ years’ experience in GMP analytical work within pharma/biotech—covering analytical method development and validation, product specifications, deviation investigations, and change control; ideally in QA supporting QC (or as a QC Coordinator/similar). Broad knowledge of analytical chemistry and bioassays, including clear and compliant documentation practices. Professional proficiency in English, written and spoken. You live the Sobi CARE values: Care, Ambition, Urgency, Ownership and Partnership. Ability to work independently, take initiative, and make sound quality decisions. Strong communication skills and a collaborative, team-oriented approach. A structured mindset with attention to detail and a commitment to continuous improvement. Here at Sobi we live by our core values: Care, Ambition, Urgency, Ownership and Partnership! Additional Information How to apply We have an ongoing selection process in this recruitment and ask you to send your application as soon as possible. Click apply and include your resume. Why Join Us? Here at Sobi, our mission and culture get us excited to come to work every day, but here are a few more reasons to join our team: Collaborative and team-oriented environment Opportunities for professional growth Diversity and Inclusion Competitive compensation for your work Making a positive impact to help ultra-rare disease patients who are in need of life saving treatments Emphasis on work/life balance Sobi is a global company with over 1,900 employees in more than 30 countries and are committed to the societies where we operate. We are a specialised international biopharmaceutical company transforming the lives of people with rare and debilitating diseases, providing reliable access to innovative medicines in the areas of haematology, immunology, and specialty care. Sobi’s share is listed on Nasdaq Stockholm. More about Sobi at sobi.com and LinkedIn. We know our employees are our most valuable asset and our culture conveys that. We offer a competitive benefits package, to support the health and happiness of our staff. Sobi Culture At Sobi, we refuse to accept the status quo. This is because we have witnessed first-hand the challenges facing those affected by rare diseases and have used this knowledge to shape our business to find new ways of helping them. As a specialized biopharmaceutical company, we are dedicated to rare diseases. And we see this focus as a strength. By effectively turning our research into ground-breaking treatments, we help make medicine more accessible and open more possibilities for patients and more opportunities for those caring for them. This has been our approach since day one, but we know we can’t change the world of rare diseases on our own. Accomplishing this requires strong partnerships with patients, partners and stakeholders across the entire value chain. Together, we define how our business can create solutions that serve the needs of those affected by rare diseases while facilitating sustainable growth. Sobi Location: Sweden

Responsibilities

The QA Analytical Specialist acts as a quality partner for analytical activities and stability studies, ensuring GMP compliance for clinical and commercial supply. Responsibilities include managing deviations, CAPA, change controls, and providing quality oversight for analytical method validation and technology transfers.