4 дня назад
Facilities Coordinator (Biotech)
35 - 40$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Facilities Coordinator (Biotech): Inducting and managing pharmaceutical, biotech, and medical-device facility assets in the Blue Mountain RAM system with an accent on asset hierarchies, preventive maintenance, calibration planning, and GMP data integrity. Focus on coordinating project handovers, reconciling physical equipment records, maintaining inspection-ready documentation, and supporting facilities vendors and site operations.
Location: Onsite in Irvine, United States
Salary: $35–$40 per hour
Company
provides consulting and operational services to life sciences organizations, supporting the compliant development, manufacturing, and distribution of healthcare products.
What you will do
- Lead the end-to-end induction of new, relocated, and modified equipment, utilities, and facility assets into Blue Mountain RAM.
- Collect and verify equipment lists, technical data, P&IDs, manuals, spare parts lists, calibration certificates, and turnover packages.
- Create asset records, functional hierarchies, parent-child relationships, GMP impact classifications, and criticality assessments.
- Set up preventive maintenance and calibration plans, frequencies, tolerances, and job plans with Maintenance and Metrology.
- Coordinate physical asset tagging, field walkdowns, data-quality audits, asset retirement, and change-control records.
- Schedule vendor and contractor visits and support access, permits, safety orientation, facilities requests, space moves, and shutdown planning.
Requirements
- Associate’s or bachelor’s degree in Engineering, Facilities Management, Life Sciences, or a related field, or equivalent work experience.
- 3+ years of facilities, maintenance, or asset-management experience in a regulated pharmaceutical, biotech, or medical-device environment.
- Experience inducting assets into a CMMS, including building asset hierarchies, entering technical data, and configuring preventive-maintenance and calibration schedules.
- Working knowledge of cGMP, GDP, 21 CFR Part 11, and ALCOA+ data-integrity principles.
- Strong attention to detail, organization, and ability to manage multiple induction packages simultaneously.
Nice to have
- Experience with calibration-management and metrology programs.
- Knowledge of Veeva Vault, TrackWise, or MasterControl change-control and QMS systems.
- Knowledge of reliability concepts, including criticality assessments, RCM, and spare-parts strategy.
- CMRP, CAMA, or IAM certification.
Culture & Benefits
- 9-month W2 temporary assignment with potential extension.
- Medical and sick-time benefits are included for W2 temporary roles.
- Work alongside multidisciplinary project, CQV, Engineering, Maintenance, Metrology, Quality, and vendor teams.
- Professional development and coaching opportunities within a multicultural international organization.
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