Data Steward - Associate Principal Scientist, Analytical R&D

GQLMAS Data Steward

The GQLMAS Data Steward will support implementation of standard digital solutions for analytical method transfer, analytical method execution and assay monitoring in the QC network. This will involve collaboration with key partner groups in our company to define solutions and implement them across the QC network.

In this role, the Data Steward will work with the Analytical Program Lead (APL) to ensure that digital solutions are available to support QC laboratories operating in a consistent manner using standard global analytical documentation. Data management and visualization will be supported to ensure data is available on demand for all necessary purposes across the network. This will include both assay monitoring and data trending (e.g. release data and proactive process analysis (PPA) data).

Furthermore, the Data Steward will organize external data oversight (from CMOs and CTLs) and will support the APL in the management of stability data for filing and response-to-question (RtQ) purposes.

• Support the creation of digital method and assay monitoring solutions across the end-to-end analytical lifecycle in our company to QC laboratories. Collaborate with partners to support technology deployment and method implementation in a standard manner to all QC testing nodes.
• In collaboration with MS&T and QC partners, develop standard processes to collect, organize, analyze and interpret analytical release, stability and in-process data across internal and external testing nodes.
• Support maintenance of standard execution approaches across testing nodes via digital solutions.
• Support change control for digital methods to ensure changes are rigorously reviewed and implemented in a standard manner across QC testing nodes.
• Support creation of data reporting tools to facilitate regulatory filings, RtQ, stability period assignment, investigations and analytical method performance verification.

• MSc-level education or equivalent through experience
• At least 7 years' experience in the pharmaceutical industry
• Basic understanding of the product development trajectory, regulatory filing requirements and existing regulatory GMP requirements (ICH, pharmacopeia)
• Affinity for digital solutions for assay monitoring and data trending
• Proven proactive, service-oriented and collaborative mindset
• High personal integrity, credibility and energy
• Excellent communication skills (verbal and written)

Adaptability, Analytical Method Development, Analytical Method Transfer, Assay, Assay Development, Biochemical Assays, Biological Assay Development, Cell-Based Assays, Chromatographic Techniques, Collaborative Development, Cross-Functional Teamwork, Data Monitoring, Data Stewardship, External Collaboration, GMP Compliance, High-Performance Liquid Chromatography (HPLC), Optimism, Pharmaceutical Management, Process Analytical Technology (PAT), Product Development, Protein Analysis, Quantitative Assay, Strategic Collaborations, Teamwork

The salary range for this role is $ - $

This is the lowest to highest salary we in good faith believe we would pay for this role at the time of this posting. An employee's position within the salary range will be based on several factors including, but not limited to relevant education, qualifications, certifications, experience, skills, geographic location, government requirements, and business or organizational needs.

The successful candidate will be eligible for annual bonus and long-term incentive, if applicable.

We offer a comprehensive package of benefits. Available benefits include medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days. More information about benefits is available at .

You can apply for this role through (or via the Workday Jobs Hub if you are a current employee). The Final date to receive applications for this position is stated on this posting.