Analytical Science & Technology Technical Lead at Sobi

Stockholm, , Sweden -

Full Time

Start Date

Immediate

Expiry Date

19 Jul, 26

Salary

0.0

Posted On

20 Apr, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Analytical chemistry, Biochemistry, Pharmacist, Chemical engineering, Biological drugs, Validation, Analytical tech transfer, Stability studies, HPLC, Spectroscopy, ELISA, Bioassay, GMP, Regulatory filing, CAPA, Quality management

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 Join Sobi’s Global CMC Science & Technology team and help shape how our medicines are developed and supplied worldwide. We’re hiring an Analytical Science & Technology (Analytics) Specialists who will take a leading analytical role across our project and product portfolio. Working cross-functionally with colleagues throughout Sobi—and in close partnership with external contract manufacturing organizations (CMOs) globally—you’ll ensure our analytical methods remain compliant, robust, and fit for purpose, while also driving method transfers, validations, and continuous improvements. You’ll coordinate stability studies and support investigations and quality activities (deviations, changes, and CAPAs), acting as an Analytical Subject Matter Expert (SME) to help deliver reliable products to patients. This is a remote role located within the European time zone, reporting to Group Head Analytics based in Sobi HQ, Stockholm. Key Responsibilities Be able to act as Analytics product responsible taking overall responsibility for analytical methods and analytical related work for the specific product in e.g. the virtual plant teams Responsible for analytical method transfers, validations as well as supporting product stability and shelf life through ongoing stability studies Establishment and maintenance of reference materials and responsibility for product specific method standards and qualified materials (critical reagents) Ensure life cycle management, compliance, robustness, and relevance of analytical methods Act as SME in work with regulatory filing, new launches as well as the ongoing work with supply of the commercial products Support investigations of deviations, changes and CAPAs, complaints, out of trends (OOT) and out of specifications (OOS) Qualifications Qualifications MSc/PhD, analytical chemistry/chemistry/biochemistry/pharmacist/chemical engineering or similar +5 years of experience of Life Science/Pharma industry with commercial products Experience of analysis of biological drugs, validation, analytical tech transfer, stability studies, specifications, handling of reference standards and critical reagents. Skilled in common QC methods in the laboratory, e.g. any of HPLC, spectroscopy, ELISA, bioassay Experience of working with contract manufacturer with CMOs and CLOs Experience of GMP English is required and Chinese highly preferred. 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 in English. 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: Emphasis on work/life balance 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 We are a global company with over 1,900 employees in more than 30 countries and are committed to the societies where we operate. With a deeply skilled management team directing our day-to-day wins, and a Board with a stellar track record, we’re ready to take on the world’s diseases, ailments and adversity. Our people believe they have the power to make a positive impact in others’ lives because that’s exactly what we do here. If you’re seeking a career that taps into your talents in a way that makes the world a better, healthier place, we just may have a job for you. 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 up 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 Technical Lead will manage analytical methods, method transfers, and validations while acting as a Subject Matter Expert for product stability and regulatory filings. They will work cross-functionally and with external CMOs to ensure compliance, robustness, and continuous improvement of analytical processes.