Description:

Fabrication, inspection, and metrology, testing and troubleshooting components and instrumentation.

Document, report, and present results of experiments and procedures.

Recommend improvements for related processes while maintaining GLP/GMP practices and reagent conformity.

Follow work instructions and Standard Operating Procedures (SOPs) as required by ISO 13485:2016 quality management systems.

Complete routine activities within the laboratory and workshop including equipment maintenance.

Skills:

iso 13485, troubleshooting, instrumentation, repair

Additional Skills Qualifications:

7+ years of engineering technician experience

Lead/supervisory experience is a plus

Development experience including testing, verification activities, generating documentation, and product technical transfer preferred.

Specific work experience in medical devices or pharmaceutical regulated environment (i.e., ISO 13485) desired.

Experience with Lean/Six Sigma methods.

Practical experience in rapid prototyping techniques (e.g., CNC milling, 3D printing, laser cutting, plastic bonding techniques).

3D CAD design (Solidworks).

Experience Level:

Expert Level

About Actalent

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.

Diversity, Equity Inclusion

At Actalent, diversity and inclusion are a bridge towards the equity and success of our people. DEI are embedded into our culture through:

Hiring diverse talent

Maintaining an inclusive environment through persistent self-reflection

Building a culture of care, engagement, and recognition with clear outcomes

Ensuring growth opportunities for our people

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 [email protected] (%[email protected]) for other accommodation options.