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Description:
Responsible for troubleshooting production, receiving inspection, complaint investigations, NCMRs
working on manufacturing line, inspecting product and ensuring compliance
Documenting sterile load release and inspection once a month
completing risk assessments and NCMRs
collaborating with team members on different initiatives
Skills:
risk assessment, complaint analysis, Manufacturing engineering, Manufacturing process, Capa, Medical device, Process improvement, capital equipment
Qualifications:
Must Haves
Bachelors' in Engineering
2 years experience in Engineering
medical device or other regulated industry (pharmaceutical, food)
Nice to Haves
CAPA
Medical Device
Catheter or Neuro Experience
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.
At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DE&I are embedded into our culture through:
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.
Other
$91k-111k (estimate)
06/26/2024
08/25/2024