Skip to main content
Tallo logoTallo logo

Find Jobs

Find Jobs Near You – Available Work in Your Location

Skip to job details

Back to Results

Apply for this opportunity

To apply for this job, you'll continue to an external website or email application.

Noramtec Consultants Americas

Manufacturing Engineer (Validation)

Career Insights for Validation Engineer

See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.

Scorecard

Based on Indiana data

Review key factors to help you decide if this role fits your goals. How is this calculated?

Were these scores useful?

What they do

A Validation Engineer evaluates and maintains machinery and equipment used in manufacturing, and supervises workers that use and repair the machines.

$94,546 / year median in Indiana

-2% projected decline

Explore Career

Job Description

Our client is a global leader in musculoskeletal healthcare. They design, manufacture and market orthopedic reconstructive products; sports medicine, biologics, extremities and trauma products. Their products and solutions help treat patients suffering from disorders of, or injuries to, bones, joints or supporting soft tissues. Alongside some of the world's top healthcare professionals, they help deliver new possibilities to patients.
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. Expected Areas of Competence (i.e., knowledge, skills and abilities) 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. Education/Experience Requirements B.S. in Engineering with a minimum of 3-year experience in validation in pharmaceutical/biotech manufacturing.
Pay:
Up to $42.00 per hour
Benefits:
401(k) Dental insurance Health insurance Vision insurance
Work Location:
In person