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Sobi

Develops therapies for rare diseases

External Quality Operations Manager

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeNo salary listed

About the Job

Requirements

  • A university degree or similar in a relevant area such as pharmaceutical, biotech, or life science is required.
  • More than 5 years of experience within pharmaceutical or biotech products, with experience in QA operations, production, or another relevant area such as GMP or GDP.
  • More than 1 year of experience managing external quality oversight of CMOs.
  • A curriculum vitae is required to evaluate batch release qualification.
  • Fluently spoken and written English is required.

Responsibilities

  • Act as the single point of contact for all quality-related activities at the Contract Manufacturing Organization (CMO).
  • Ensure that handling, manufacturing, and distribution of products comply with the Sobi Quality System, the effective Quality Technical Agreement, and relevant current Good Manufacturing Practice regulatory requirements.
  • Support product release by acting as a Qualified Person (QP) delegate according to delegation documents when necessary.
  • Support qualification of External Service Providers (CMOs).
  • Ensure that Quality Technical Agreements (QTAs) are appropriately established and validly define roles and responsibilities between Sobi and the external supplier.
  • Ensure implementation and maintenance of Quality Risk Assessments and key performance indicators for external quality activities; guide the definition and monitoring of remediation plans; and drive or support process and product quality performance improvements.
  • Ensure that CMOs provide product reviews or data, including Annual Product Quality Reviews/Product Quality Reviews and stability reports, as specified in the QTA, and assess product and process performance against Sobi requirements.
  • Manage and approve quality issues, including deviations, corrective and preventive actions, and complaints, according to the QTA and Sobi requirements.
  • Ensure that change requests from the CMO or Sobi are managed according to the QTA and Sobi requirements.
  • Support quality audits of the CMO in accordance with Sobi requirements and the QTA.
  • Lead the definition of implementation and monitoring strategies for key Quality transformation initiatives and align with process stakeholders outside the Quality organization.
  • Lead or act as the Quality representative in CMO-related projects such as technology transfer and launch.
  • Assess and ensure CMO readiness for Health Authority inspections.
  • Support Health Authority inspections and audits of Sobi.
  • Inform the line manager and cross-functional teams of all critical and major issues, and escalate issues according to Sobi's escalation policy.
  • Maintain good collaboration within Global Quality Operations and cross-functionally.

Desired Qualifications

  • More than 2 years of experience working in a global operations environment with English as a main language.
  • Proven experience leading Quality KPI assessment and improvement at CMOs.
  • A proven track record with the FDA, EMEA, or other Health Authorities.
  • A strong understanding of risk assessment and risk management fundamentals and tools.

About the Company

Sobi

Develops therapies for rare diseases

Sobi specializes in developing and delivering therapies for rare diseases. It focuses on hematology, immunology, and specialty care, bringing medicines to patients who have limited treatment options. Their products are designed to treat rare conditions and are typically administered by prescription under medical supervision; the company collaborates with partners to advance research, develop, and commercialize these therapies. Sobi differentiates itself through its strong biotechnological foundation from its Biovitrum heritage and a track record of strategic collaborations with major pharmaceutical players like Sanofi and Apellis, which expand its research capabilities and reach. The company’s goal is to improve the lives of patients with rare diseases worldwide by creating and delivering effective treatments that address unmet medical needs.

Company size
1,001-5,000
Company stage
IPO
Headquarters
Solna kommun, Sweden
Founded
1988

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