9 дней назад
Senior Manager, Systems Automation (Pharmaceutical Manufacturing)
121 100 - 231 000$
Мэтч & Сопровод
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Описание вакансии
Текст:
TL;DR
Senior Manager, Systems Automation (Pharmaceutical Manufacturing): Leading a technical automation team that supports manufacturing systems, deviation investigations, validation, and large-scale performance improvement projects with an accent on compliant and reliable automation in a pharmaceutical manufacturing environment. Focus on designing and troubleshooting networked systems, managing software lifecycle documentation under cGMP and GAMP 5, and coordinating cross-functional quality and engineering work.
Location: Menands, New York, United States; onsite Monday–Friday, 8:00 a.m.–4:30 p.m. Travel to Ireland: 5–10%.
Salary: $121,100–$231,000 annually.
Company
is a biotechnology company that develops and commercializes medicines for serious diseases.
What you will do
- Lead and develop a technical automation team, managing performance, development, delegation, and delivery.
- Provide automation systems support for manufacturing and support areas and coordinate investigations into deviations and system anomalies.
- Lead corrective-action and systems-performance improvement projects using production, operational, and business data.
- Review lifecycle documentation, software testing, protocols, system test plans, change controls, and validation projects.
- Create, maintain, and approve SOPs, software lifecycle documentation, design documents, technical evaluations, and test plans.
- Design, configure, and troubleshoot networked systems while managing project portfolios, metrics, reports, and cross-functional communication.
Requirements
- Bachelor’s degree in Engineering, Computer Science, or a related field.
- Manager level: 7+ years of experience in software, database, and computerized-systems design, configuration, administration, and management.
- Senior Manager level: 8+ years of relevant experience; level depends on qualifications.
- Experience with PI Historian and Rockwell applications; familiarity with PLC, HMI, historian, and product-testing software is strongly preferred.
- Strong skills in software lifecycle documentation, design documents, technical evaluations, and test plans following cGMP and GAMP 5 guidelines are preferred.
Nice to have
- Experience in a pharmaceutical or biopharmaceutical manufacturing facility.
Culture & Benefits
- Inclusive workplace with equal employment opportunity.
- Comprehensive rewards may include bonuses, equity awards, retirement benefits, health and wellness programs, insurance, paid time off, and family support benefits.
- Background checks may verify identity, right to work, and educational qualifications.
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