Jobs at Merit Medical Systems, Inc.

Provides executive and administrative support to the EMEA leadership team during a nine-month onsite contract. Responsibilities include calendar and travel coordination, meeting preparation, stakeholder communication, confidential file management, data collection, reporting, presentations, project planning, timeline monitoring, process improvement, and cross-departmental coordination.

Leads process engineering support for medical device manufacturing, including automation projects, equipment upgrades, maintenance, calibration, validation, and continuous improvement. Improves machine uptime, yield, output, quality, process capability, and OEE while managing engineering resources, capital expenditures, risk assessments, and compliance. Collaborates with production, technical teams, suppliers, plants, and regulatory stakeholders to maintain safe, efficient, and compliant operations.

Develops and closes business relationships for oncology medical devices across the Northeast region. Presents and demonstrates products, manages new and existing accounts, negotiates pricing and contracts, resolves customer issues, prepares customized drawings and sales reports, and identifies opportunities to increase sales and market share. Requires extensive travel, strong presentation and communication skills, medical equipment knowledge, independent judgment, and at least five years of direct sales experience, preferably selling medical products.

Performs advanced engineering problem-solving, makes technical decisions, develops prototypes, writes engineering change notices, supports special projects, and may supervise technicians. The role requires independent application of analytical and scientific principles, teamwork, strong organizational skills, computer proficiency, and knowledge of applicable U.S. and international standards in a medical device environment.

Perform audits of production and finished medical products to verify compliance with Device Master Record/QSR/GMP. Generate, document, and close nonconformances (NCs), complete final inspection paperwork, review work orders/ECNs, segregate discrepant product, and operate basic test equipment to confirm product meets specifications.

Supervise clean room production teams to meet work orders and quality standards. Assign work, manage paperwork, maintain clean room, coordinate with QA, train staff, evaluate performance, and improve processes to achieve production and profitability goals.

The Senior Compliance Manager oversees compliance programs across the EMEA region, ensuring adherence to regulations and improving compliance practices. Responsibilities include risk assessment, policy development, compliance training, investigations, and regulatory knowledge management.

The Senior Director of Quality Assurance leads departments ensuring quality policies, manages quality systems, and collaborates with global teams to enhance operational efficiency and compliance in medical device production.

Sell and promote Merit medical devices across South Africa, build and maintain customer relationships, demonstrate products, prepare custom kits and pricing, resolve delivery/manufacturing issues, coordinate with marketing/sales, meet sales targets, prepare monthly reports, participate in trainings, and travel extensively to clients.

The Territory Manager will sell medical devices, achieve sales targets, maintain customer relationships, present products, and collaborate with teams. Extensive travel is required.

Sell and support Merit medical products to new and existing OEM clients. Build relationships, demonstrate products, prepare custom drawings and pricing, resolve delivery/manufacturing issues, coordinate with internal teams, meet sales targets, produce reports, and travel extensively to client sites.

The Operations Associate I assembles medical devices, performs quality inspections, verifies orders, and adheres to safety standards as part of a production team.

Serve as the primary HR contact for assigned groups, advising leaders on employee relations, performance management, investigations, compliance, training, workforce analytics, and HR process improvements to support business objectives.

Lead development and validation of manufacturing processes, equipment and fixtures for vascular medical devices. Collaborate with R&D, operations and vendors to ensure designs are manufacturable and regulatory-ready, execute risk assessments and process qualifications (IQ/OQ/PQ), and mentor junior engineers and technicians.

Perform monthly invoice payments, approve expense reports, assist with month-end close and financial recordkeeping, process sales tax returns, research problem accounts, prepare month-end balancing reports, and support department projects and other accounting tasks.

Supervise clean-room production teams to meet work orders and quality and cleanliness standards. Assign and review work, manage paperwork, coordinate with QA, train and evaluate staff, hire and manage personnel actions, identify process improvements, and support shift supervision and production performance goals.

Plan and schedule finished goods and sub-assemblies using Oracle/ASCP to balance demand and supply, manage DC inventory, process internal orders, perform allocations, monitor expirations, prepare KPI reports, support S&OP, continuous improvement, and cross-functional coordination to meet customer demand.

Lead design transfer activities ensuring design outputs translate to manufacturing. Coordinate risk management, ECNs, validations, nonconformance investigations, audits, and quality system improvements while mentoring staff.

Designs and develops medical device components and prototypes, evaluates and applies engineering techniques, investigates technical variables, writes ECNs, supports NCMR corrective actions, may supervise technicians, and works on special projects under broad direction.

Manage corporate communications channels and editorial systems, own editorial calendars and workflows, serve as primary editor for clarity and brand compliance, draft press releases and coordinate approvals, track channel performance, and provide operational support for internal and external communications.