4 дня назад
Associate Engineer (Biopharmaceutical Manufacturing)
73 245 - 99 096$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Associate Engineer (Biopharmaceutical Manufacturing): Supporting process systems, equipment maintenance, reliability, and operational improvements at a commercial and clinical manufacturing site with an accent on troubleshooting, commissioning, qualification, and predictive maintenance. Focus on analyzing equipment data, resolving process and control issues, improving maintenance systems, and supporting critical operations through a rotating 24/7 on-call schedule.
Location: US - Rhode Island - West Greenwich; onsite role with rotating 24/7 on-call support, including nights, weekends, and holidays as needed
Salary: $73,245.35–$99,096.65 annually
Company
is a biotechnology company developing, manufacturing, and delivering medicines for serious illnesses across oncology, inflammation, general medicine, and rare disease.
What you will do
- Provide daily process, equipment, maintenance, and reliability engineering support for commercial and clinical manufacturing systems.
- Troubleshoot process equipment and control issues, identify performance problems, and implement corrective solutions.
- Coordinate with Manufacturing, Process Engineering, Process Development, Utility Operations, Maintenance, Quality Assurance, and Validation teams.
- Support the design, construction, startup, commissioning, qualification, and improvement of new or modified systems.
- Analyze operational, maintenance, and engineering data; communicate findings, recommendations, project progress, and issues.
- Improve Maximo equipment records, job plans, spare-parts data, safety information, preventive maintenance, and condition-based maintenance practices.
Requirements
- High school diploma or GED with 6 years of engineering experience, an associate degree with 4 years of engineering experience, or a bachelor’s degree.
- Bachelor’s degree in engineering or a related technical field is preferred.
- Strong written and verbal communication, analytical, interpersonal, and facilitation skills.
- Ability to work with minimal direction and collaborate effectively across cross-functional teams.
- Ability to participate in a rotating 24/7 on-call schedule and support shutdowns, investigations, critical operations, and occasional off-hours issues.
- Experience with mammalian cell culture, protein purification, clean utilities, CIP, SIP, production services, non-GMP utilities, or biopharmaceutical manufacturing equipment is preferred.
Culture & Benefits
- Collaborative, innovative, science-based working environment focused on serving patients.
- Comprehensive health, dental, vision, life, disability, and flexible spending benefits.
- Retirement and savings plan with company contributions.
- Discretionary annual bonus program and stock-based long-term incentives.
- Paid time-off plans and career development opportunities.
- Onboarding lasts approximately 2–6 weeks and covers site operations, engineering systems, quality processes, and safety expectations.
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