Manufacturing Engineer I
Tekwissen
Overview:
TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. Client is a publicly traded medical device company. Client designs, develops, manufactures and markets orthopedics products, including knee, hip, shoulder, elbow, foot and ankle artificial joints and dental prostheses. client has operations in more than 40 countries around the world
Job Title: Manufacturing Engineer I Work Location: Warsaw, IN, 46580 Duration: 12 Months Job Type: Temporary Assignment Work Type: Onsite Job Description: Principal Duties and Responsibilities:
TekWissen® Group is an equal opportunity employer supporting workforce diversity.
TekWissen Group is a workforce management provider throughout the USA and many other countries in the world. Client is a publicly traded medical device company. Client designs, develops, manufactures and markets orthopedics products, including knee, hip, shoulder, elbow, foot and ankle artificial joints and dental prostheses. client has operations in more than 40 countries around the world
Job Title: Manufacturing Engineer I Work Location: Warsaw, IN, 46580 Duration: 12 Months Job Type: Temporary Assignment Work Type: Onsite Job Description: Principal Duties and Responsibilities:
- Responsible for the development, execution, and management of installation, qualification, and validation documents and protocols for process equipment
- Support a wide variety of Equipment qualifications including CNC machines
- Guide, mentor, and cross-train team members to broaden validation capabilities, including equipment and process validation
- Create change requests in windchill to support equipment moves
- Execute to project plans and schedules for work activities.
- Communicate (written and verbal) with appropriate personnel from other departments.
- This is not an exhaustive list of duties or functions and might not necessarily comprise all of the essential functions for purposes of the Americans with Disabilities Act.
- Strong knowledge of cGMP regulations, including FDA, EMA and ISO requirements
- Experience writing and executing validation protocols and reports, including IQ/OQ/PQ documentation
- Proficiency with validation of manufacturing equipment, utilities, cleaning processes and computer systems
- Good problem-solving skills through the use of quality and statistical tools.
- Ability to effectively work within a cross-functional team to complete critical project tasks.
- Demonstrates good written and verbal communication skills.
- Strong technical writing and documentation skills
- Ability to independently develop and execute on project plans.
- Demonstrated ability to take initiative and provide recommendations on process, procedure and training.
- B.S. in Engineering with a minimum of 3-year experience in validation in pharmaceutical/biotech manufacturing.
- Bachelor's Degree and 0 years of relevant experience, or Associate's Degree and 2 years of relevant experience, or High School Diploma or Equivalent and 4 years of relevant experience
TekWissen® Group is an equal opportunity employer supporting workforce diversity.
Vacancy posted 1 day ago
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