Purpose And Scope
The SCM compliance specialist SPD is responsible for the department quality management system. Keeps all documentation up to date, lead the quality process improvements and reports the quality performance. The specialist is organizing the risk management process and all investigations till closure
Responsibilities And Accountabilities
- Responsible for maintaining a document management system compliant with GxP requirements.
- Performs QA document control functions, including document issuance, reconciliation, distribution, release, and archiving of documents.
- Responsible for ensuring Data Integrity within the SPD Group.
- Learning Management System (LMS) key contact, maintain training matrix, owner of curricula within LMS.
- Ensures accuracy by reviewing documents for completeness, proper authorization, and impact to other quality systems.
- Collaborates with cross-functional departments to ensure timely implementation of document change requests.
- Lead Investigations of Non-conformances related to SPD processes and develops effective corrective action plans in collaboration with internal and external stakeholders.
- Contribute to Non-Conformances and CaPa outside SPD, impacting SPD group processes.
- Assist in providing training to new staff on document management processes and procedures.
- Supports audits (internal, external) to verify that regulatory and quality requirements have been met.
- Coordinates the revision, review, and approval and obsoletion of SOPs and other GMP documents. Responsible for ensuring periodic reviews of all related documents and SOPs.
- Performs other duties as assigned or special projects as needed.
- Organize and lead the Risk management process.
- Responsible for periodic quality KPI reporting
- Responsible for organizing, preparing, and documenting the periodic quality management review
Required Qualifications
Education : bachelor's degree or equivalentExperience of working in a GxP organization : more than 3 yearsExperience with Electronic Document Management Systems.Excellent communication and interpersonal skills. Excellent judgment, problem resolution & teamworkAbility to work independently without significant oversight or instruction to achieve results with a high degree of accuracy and attention to detail.Cross-functional collaboration skills, able to build friendly cooperative relationships (including external parties)Preferred Qualifications
Experience using document management software in a regulated industry.Proficiency in MS Excel, PowerPoint, and / or Visio to include creation / formatting of charts and data tables.Experience in an environment subject to regulatory audits / inspections.Knowledgeable about SAP, Veeva Vault, Track Wise and / or other commonly used tools within GxP environment.Experience of working in project organizationsBasic knowledge and understanding of supply chain processes.Working Environment
Astellas' Global Capability Centres (GCCs) are strategically located sites that give Astellas the ability to access talent across various functions in the value chain and to co-locate core capabilities that are currently dispersed. Our three GCCs are located in India, Poland and Mexico.
The GCCs will enhance our operational efficiency, resilience and innovation potential, enabling a timely response to changing business demands.
Our GCCs are an integral part of Astellas, guided by our shared values and behaviors, and are critical enablers of the company's strategic priorities, sustainable growth, and commitment to turn innovative science into VALUE for patients.
Category Supply Process Development
Astellas is committed to equality of opportunity in all aspects of employment.
EOE including Disability / Protected Veterans
Skills Required
Ms Excel, Sap, Powerpoint, Visio