Click or tap here to enter text.Do you want to be part of an inclusive team that works to develop innovative therapies for patients? Every day, we are driven to develop and deliver innovative and effective new medicines to patients and physicians. If you want to be part of this exciting work, you belong at Astellas!
Astellas Pharma Inc. is a pharmaceutical company conducting business in more than 70 countries around the world. We are committed to turning innovative science into medical solutions that bring value and hope to patients and their families. Keeping our focus on addressing unmet medical needs and conducting our business with ethics and integrity enables us to improve the health of people throughout the world. For more information on Astellas, please visit our website at www.astellas.com.
About Astellas Gene Therapies
Astellas Gene Therapies is an Astellas Center of Excellence developing genetic medicines for patients with rare, life-threatening diseases. Based on our innovative approach to developing genetic medicines, as well as our industry-leading internal manufacturing capability and expertise, we have become the Astellas Center of Excellence for their newly created Genetic Regulation Focus Area. We are currently exploring three gene therapy modalities: gene replacement, exon skipping gene therapy, and vectorized RNA knockdown, with plans to expand our focus and geographic reach under Astellas. We are based in San Francisco, with manufacturing and laboratory facilities in South San Francisco and Sanford, North Carolina. For more information, please visit our website: www.astellasgenetherapies.com.
The Role:
The Senior Specialist, QC Systems Support will be responsible for defining requirements, implementation and maintenance for QC support processes and systems including sample and data management (including stability study management and contract lab coordination), as well as investigations, change controls and document revisions. This role will also define, implement and maintain the departmental training program. This role will work closely with the multiple QC groups including Quality Assurance and Manufacturing. This roles primary function will be to support QC investigations and support other operations in QC.
Responsibilities:
Quantitative Dimensions:
The QC Specialist IV, QC Systems Support will be responsible for defining requirements, implementation and maintenance of Quality Control lab processes and systems including sample and data management, as well as processing QC requests/actions for investigations, change controls and document revisions.
Organizational Context:
The QC Systems Support, QC Specialist IV will typically report to the Lead, Quality Control Systems Support. This role is expected to Model our Core Values and to demonstrate work performance as someone who exemplifies the culture we want to create; operates with transparency; is trusted; and supports the overall mission and vision of Astellas Gene Therapies and the Astellas organization.
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