2 дня назад
Injection Process Manager (Medical Devices)
120 000 - 140 000$
Мэтч & Сопровод
Для мэтча с этой вакансией нужен Plus
Описание вакансии
Текст:
TL;DR
Injection Process Manager (Medical Devices): Leading injection molding process engineering across multiple sites, including mold installation, validation, ramp-up, optimization, and lifecycle management for medical device components with an accent on scientific molding, equipment qualification, and regulatory compliance. Focus on managing processing engineers, solving complex molding problems through root cause investigations, and implementing corrective and continuous improvement initiatives.
Location: Buffalo Grove, Illinois, United States; onsite work in an office and clean manufacturing environment
Salary: $120,000–$140,000 USD per year
Company
is a global manufacturer of drug delivery systems and medical device components for the pharmaceutical industry, with manufacturing sites in the United States, France, Germany, Brazil, and Poland.
What you will do
- Lead injection molding process engineering and processing activities across multiple plastic injection molding sites.
- Manage project-specific injection teams, including planning, workload allocation, performance indicators, recruitment needs, onboarding, and training.
- Oversee process development, optimization, troubleshooting, validation, equipment qualification, and lifecycle management for injection molds and molding solutions.
- Support specifications for injection molding machines, molds, and plastic preparation and regulation peripherals.
- Lead root cause investigations, corrective actions, lean initiatives, and continuous improvement projects.
- Coordinate technical file transfers, production team training, internal project reviews, and client project meetings.
Requirements
- Bachelor’s or master’s degree in engineering or a similar technical field.
- Minimum 3–5 years of supervisory experience in plastics manufacturing and 7+ years of injection molding processing experience.
- Strong knowledge of scientific molding methodologies and high-volume plastic injection molding production.
- Experience qualifying complex, tight-tolerance injection molds and supporting high-volume production.
- Strong knowledge of regulatory requirements, including FDA and ISO standards.
- Must be eligible to work in the United States. Clear and well-organized oral and written communication is required.
Nice to have
- Experience in a cGMP- and ISO 13485-compliant manufacturing environment.
- Leadership experience with the ability to mobilize individual and collective efforts.
- Excellent problem-solving skills using DMAIC methodology.
- Strategic thinking.
Culture & Benefits
- Opportunity to work in an international medical device manufacturing group.
- Work environment includes office areas, clean manufacturing areas, moderate noise, PPE, and cleanroom apparel.
- US employee benefits are offered.
- Work contributes to the development of drug delivery devices designed to improve patient treatment adherence.
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