Description

Ensure compliance with FDA, ISO 13485, and other regulatory standards by conducting inspections, audits, and risk management activities.

Develop, implement, and maintain quality control procedures and documentation to uphold manufacturing excellence.

Fully competent engineer in all conventional aspects of the subject matter, functional area, and assignments.

Plans and conducts work requiring judgment in the independent evaluation, selection, and substantial adaptation and modification of standard techniques, procedures, and criteria.

Devises new approaches to problems encountered.

Independently performs most assignments with instructions as to the general results expected.

Receives technical guidance on unusual or complex problems and supervisory approval on proposed plans for projects.

Plans, schedules, conduct, and coordinates detailed phases of engineering work in part of a major project or in a total project of moderate scope.

Performs work that involves conventional engineering practice but may include a variety of complex features such as conflicting design requirements, unsuitability of conventional materials, and difficult coordination requirements.

Work requires broad knowledge of precedents in the specialty area and good knowledge of principles and practices of relates specialties.

May technically supervise or coordinate the work of engineers, draftspersons, technicians, and others who assist in specific assignments.

Practices company safety, quality policies and procedures, actively requires conformance.

Responsible for ensuring personal and company compliance with all Federal, State, local and company regulations, policies and procedures for Health, Safety and Environmental compliance.

Responsible for the purchase or design of equipment that meets health, safety and environmental standards set by the company.

Responsible for performing design reviews and pre-validation assessments to ensure the safe and environmentally sound start-up of new processes.

Skills & Qualifications

MUST:

-8+ Years Product Quality Engineering Experience

-Design Quality and Design Review Experience

-Risk Management

-Bachelor's Degree in STEM Field

PREFERRED:

-Lean Six Sigma

-Chemistry

-Process Validation

-Medical Device

-Masters Degree

Experience Level

Expert Level

ON SITE

Pay and Benefits

The pay range for this position is $48.07 - $62.50/hr.

Eligibility requirements apply to some benefits and may depend on your job classification and length of employment. Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following:

• Medical, dental & vision
• Critical Illness, Accident, and Hospital
• 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available
• Life Insurance (Voluntary Life & AD&D for the employee and dependents)
• Short and long-term disability
• Health Spending Account (HSA)
• Transportation benefits
• Employee Assistance Program
• Time Off/Leave (PTO, Vacation or Sick Leave)

Workplace Type

This is a fully onsite position in Miami Lakes,FL.

Application Deadline

This position is anticipated to close on Mar 13, 2025.

About Actalent

Actalent is a global leader in engineering and sciences services and talent solutions. We help visionary companies advance their engineering and science initiatives through access to specialized experts who drive scale, innovation and speed to market. With a network of almost 30,000 consultants and more than 4,500 clients across the U.S., Canada, Asia and Europe, Actalent serves many of the Fortune 500.

Diversity, Equity & Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:

Hiring diverse talent Maintaining an inclusive environment through persistent self-reflection Building a culture of care, engagement, and recognition with clear outcomes Ensuring growth opportunities for our people

The company is an equal opportunity employer and will consider all applications without regard to race, sex, age, color, religion, national origin, veteran status, disability, sexual orientation, gender identity, genetic information or any characteristic protected by law.

If you would like to request a reasonable accommodation, such as the modification or adjustment of the job application process or interviewing process due to a disability, please email actalentaccommodation@actalentservices.com for other accommodation options.