Quality Pocess Engineer

at  Heraeus Medevio

PDC, Provincia Cartago, Costa Rica -

Start DateExpiry DateSalaryPosted OnExperienceSkillsTelecommuteSponsor Visa
Immediate23 Oct, 2024Not Specified24 Jul, 2024N/AAnalytical Skills,Iso,Regulatory Compliance,Process Validation,Microsoft Office,Erp Software,Interpersonal Skills,PaddingNoNo
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Description:

QUALIFICATIONS:

Bachelor’s degree in engineering, Science, or a related field.
Knowledge of quality management systems, such as ISO 13485 and FDA standards, applicable to medical device manufacturing.
Experience with statistical analysis, process validation, and quality assurance methodologies.
Strong problem-solving and analytical skills, including familiarity with tools like FMEA, SPC, and DOE.
Excellent communication and interpersonal skills to collaborate effectively with internal and external stakeholders.
Excellent English Communications Skills
Understanding of risk management, CAPA processes, and regulatory compliance in the medical device industry.
ASQ certified Quality engineer a plus.
Ability to utilize MRP or ERP software and Statistical Analysis Software.
Root cause analysis training, Project Management, Statistical analysis, SPC, Six Sigma Tools and Geometric Dimensioning and Tolerancing experience preferred.
Proficient with Microsoft Office.
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Candidates, interested in requisition in Quality Process Engineer, are invited to apply online or contact jobs-medevio@heraeus.com for further questions – both will of course be treated confidentially

Responsibilities:

Develop and implement quality control plans and processes to ensure compliance with regulatory requirements.
Lead and oversee process improvement initiatives to enhance product quality, reduce defects, and optimize manufacturing processes.
Collaborate with cross-functional teams to identify and resolve quality issues and drive continuous improvement efforts.
Conduct root cause analysis and implement corrective and preventive actions to address quality non-conformances.
Perform risk assessments and develop risk mitigation strategies to ensure product safety and efficacy.
Provide training and guidance to production teams on quality control practices and procedures.
Monitor and analyze quality performance data to identify trends and opportunities for improvement.
Actively works within all aspects of the Quality System to provide supporting Value Stream Team.
Actively involved with Manufacturing/Engineering in the identification and resolution of product quality problems.


REQUIREMENT SUMMARY

Min:N/AMax:5.0 year(s)

Pharmaceuticals

Production / Maintenance / Quality

Clinical Pharmacy

Graduate

Engineering science or a related field

Proficient

1

Provincia de Cartago, Costa Rica