Lead the implementation & optimization of Product Lifecycle Management (PLM) systems across our global Clinical & Commercial Supply Chain.
Requirements:
Reqs Bachelor degree in Computer Science, Chemical Engineering, Biotech, or a related field + 8 yrs of experience in pharmaceutical supply chain operations, including manufacturing, distribution, & regulated workflows, w/ hands-on use of enterprise systems such as Oracle & SAP (including Oracle PLM). Alternatively, the employer will accept a Master degree in the above-listed fields + 6 yrs of experience in pharmaceutical supply chain operations, including manufacturing, distribution, & regulated workflows, w/ hands-on use of enterprise systems such as Oracle & SAP (including Oracle PLM). Must have full term of experience w/ the following: hands-on experience w/ System Development Lifecycle (SDLC) & Validation Lifecycle (VLC) methodologies, including authoring & executing validation documentation; experience in authoring & executing computer system validation activities (e.g., IQ/OQ/PQ) & managing validation deliverables in regulated environments using tools such as GTest; experience managing change control, deviations, & issue tracking within GxP-regulated systems, utilizing tools such as GVault; knowledge of data migration methodologies supporting global system implementations, including data integrity & validation reqs; proficiency in current Good Manufacturing Practices (cGMP) & regulatory standards governing electronic systems, including 21 CFR Part 11, Annex 11, & Annex 16. Telecommuting permitted up to 2 days/wk.
Compensation and Benefits:
Annual salary range for this position is $189,996 to $192,480. Compensation will vary depending on experience & qualifications, & for benefits visit: https://www.gilead.com/careers/compensation-benefits-and-wellbeing.
Application Instructions:
To apply for this role: [email protected] & ref job code DP021.
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