Technician II, Process Development

THIS POSITION IS ELIGIBLE FOR A $2,250.00 NEW HIRE SIGN-ON BONUS

JOB SUMMARY

The Technician II, Process Development is primarily responsible for providing tools and support to engineering and production while adhering to the quality and cost requirements of the company. The tools included but are not limited to written processes and procedures, equipment and fixtures, and training programs. The development of these tools must be based on sound engineering principles and be implemented in accordance with Good Manufacturing processes (GMP) and ISO standards. This position will also support other engineers and areas as needed and performs at an advanced level.

ESSENTIAL RESPONSIBILITIES

• Identifies, executes, and promotes Continuous Improvement objectives

• Assists in defining Lean Manufacturing requirements

• Develop processes and procedures for projects to improve quality and cost

• Originate and maintain written technical descriptions of processes and procedures comprehensive in scope and understandable by the audience

• Represent engineering for Material Review Board concerning material dispositions

• Represent Engineering in cross functional teams as assigned

• Maintain compliance to procedures and regulatory requirements

• Understand and follow safety policies and practices, attend safety training and wear PPE as required

• Maintains and prepares project plans to satisfy timeline requirements

• Prepares Engineering Change Orders for processes and components

• Performs Corrective and Preventative Action tasks

• Reliable, consistent, and punctual attendance is an essential function of the job

• Other Duties as assigned.

This is not a remote position.

An individual in this position must be able to successfully perform the essential duties and responsibilities listed above. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions of this position.

QUALIFICATIONS

• Bachelors degree in related technical field

• 3 Plus years experience in the engineering/manufacturing environment for medical devices

• FDA, cGMP principles and practices, (ISO 9001, ISO 13485)

• Experience with Silicone molding is a plus

• Familiarity with Pro-E / CREO and or SolidWorks is preferred.

• Strong computer skills associated with Microsoft software

• Ability to interpret technical drawing, blueprints, specification, and illustrations

• Must be able to read, write and speak fluent English.

• Excellent reading, writing, communication, and organizational skills.

• Demonstrated ability for systematic problem solving, DMAIC

WORKING ENVIRONMENT

Work is performed in an office environment. The noise level in the work environment is usually moderate. The work environment characteristics described here are representative of those an individual encounters while performing the essential functions of this position.

EEO STATEMENT

Cirtec Medical Corporation is an Equal Opportunity Minority/Female/Individuals with Disabilities/Protected Veteran and Affirmative Action Employer

Cirtec Medical Corporation considers for employment and hires qualified candidates without regard to age, race, religion, color, sex, sexual orientation, gender identity, national origin, ancestry, protected veteran or disability status or any factor prohibited by law. Cirtec Medical Corporation and all of its related companies fully endorse equal opportunity for all. Cirtec Medical provides reasonable accommodation for qualified individuals with disabilities and disabled veterans in the job application process.