Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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У роли понятная зона ответственности на senior-уровне в регулируемом производстве медизделий и конкретные задачи по операциям и улучшениям; при этом важно учитывать работу на площадке и широкий круг взаимодействия.
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Описание вакансии
Текст:
Hirify AI/Оригинал
TL;DR
Sr. Value Stream Manager (Medical Device Manufacturing): Managing value stream activities, production schedules, quality standards, material flow, and manufacturing teams with an accent on cost reduction, risk mitigation, process validation, and regulatory compliance. Focus on optimizing capacity and safety stock, resolving cross-functional production issues, improving equipment and processes, and developing teams for continuous improvement.
Location: On-site in La Garita, Costa Rica; other listed locations include Mexico, Puerto Rico, and Colombia
Company
hirify.global is a fertility and women’s healthcare company offering medical devices, assisted reproductive technology, and genomic testing solutions as a business unit of CooperCompanies.
What you will do
Manage value stream activities and employees according to production schedules, quality standards, and profit objectives.
Monitor production flow, schedules, rejected materials, scrap, safety stock, and capacity utilization.
Coordinate with supply chain, engineering, quality, manufacturing, sales, buyers, planners, suppliers, and customers to resolve production and material issues.
Review and approve engineering change notices, NCMRs, OALs, variances, CAPAs, and other quality documentation.
Lead cost improvement, risk reduction, quality improvement, communication, team development, and continuous improvement programs.
Prepare operating reports and budgets, keep the Director of Operations informed, and ensure compliance with GMP, ISO, and OSHA requirements.
Requirements
At least 8 years of experience managing a labor- and machine-intensive manufacturing environment.
Degree in Mechanical, Industrial, Chemical, Materials, or Biomedical Engineering, Microbiology, or a similar field.
Ability to communicate well in English and Spanish, orally and in writing.
Personnel management, team development, motivation, and coordination skills.
Analytical ability to collect, analyze, and communicate complex data concisely.
Understanding of equipment, equipment qualification, process validation, and medical device manufacturing requirements, including FDA and ISO 13485 requirements.
Proven record of cost reduction and work simplification, with the ability to carry improvement ideas through implementation.
Solid understanding of lean tools and strong proficiency with Microsoft Excel, Word, PowerPoint, Power BI, and related software.
Nice to have
Understanding of molding and automation processes.
Six Sigma Green Belt certification or higher.
Master’s degree in Mechanical, Industrial, or Chemical Engineering.
Culture & Benefits
Work is performed on-site in a manufacturing environment.
Focus on dedicated, innovative, friendly, collaborative conduct and doing the right thing.
Equal employment opportunity is provided regardless of legally protected characteristics.
Disability accommodations are available through Talent Acquisition.
Hiring process
Applications should be submitted directly; agencies must not contact hirify.global employees unless engaged under a valid agreement.
Employment agencies submitting candidates outside an authorized engagement will not receive a fee.
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