Medical Device Manufacturing Associate

HIRING FOR A MEDICAL DEVICE MANUFACTURING ASSOCIATE FOR A BRAND NEW PRODUCT -

please apply to join this exciting and innovative company/project!

• Opportunity for growth into shifts leads and team leads, as they continue to grow they would have the opportunity to make a move into an engineering, regulatory roles, quality roles long term.
• They will be directly involved in a very innovative product that will save many lives. The opportunity to work for a government funding project.
• They will learn more about blood products and biologics. This military kit will be sold to the DoD and used to save many peoples lives. Once it is commercialized you will see this product in hospitals, ambulances, etc.
• This is a brand new product that they will have first hand experience on getting it to commercialization.

Description:

This position will consist of transforming the frozen plasma into freeze-dried plasma.

They will be walking into the freezer to grab the frozen plasma and put it into a machine that will thaw it out. Once this is completed they will transfer the liquid plasma into another bag to put it into the lyophilizer for 7 days to extract all of the moisture to turn it into a freeze dried substance. They will repackage the plasma in the kitting room after that. Every unit is tracked in a BECS system, so attention to detail and experience in a GMP environment is needed.

When they are not spending their time in the cleanroom they will be reviewing procedure and redlining the production procedure to continuously improve it. At this point in time the majority of their time is spent working at the desk.

• Champion a safety driven culture. Ensure compliance with all safety and environment regulations.

• Manufacture, inspect, and package products following written processes.

• Work at a pace that meets, or exceeds, established time standards while making quality product.

• Build, inspect and package product following written procedures and using applicable equipment to perform basic visual, dimensional, time and documentation checks, while meeting established timed standards and production goals.

• Identify quality issues or workmanship deficiencies related to equipment, assembly and inspection processes, materials, sub-assemblies, and manufacturing environment.

• Comply with GMP requirements by maintaining individual training records, completing data entry in production records in a timely and accurate manner, and adhering to documented manufacturing practices and procedures.

• Maintain a clean, safe and organized work environment.

• Comply with all policies and procedures.

• Cross-train across multiple product lines following the Teleflex program.

• Perform other duties as assigned.

Qualifications:

GMP understanding (6+ months)

Understands how to follow SOPs

Computer Literate (they will be logging information into a BECS system)

6+ months of relevant experience required – Biologics, Pharmaceuticals or Medical Devices

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. DE&I 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 actalentaccommodation@actalentservices.com for other accommodation options.