Asahi Kasei
Asahi Kasei
Posted 4 days ago
Internship
Glenview, Illinois
In Person
Smart Summary
Responsibilities
The Engineering Intern will assist in the design, manufacture, and qualification of custom capital equipment for pharmaceutical manufacturing. Key tasks include creating design documents, executing test protocols, and supporting commissioning and validation activities.
Qualifications
You are currently pursuing a Bachelor's or Master's degree in an Engineering field such as Mechanical, Chemical, Electrical, or Biomedical. You should possess an awareness of Quality Management Systems and demonstrate a customer-focused mindset with strong interpersonal and problem-solving skills.
Must Have Skills for ATS
technical drawings
specification documents
test protocols
GAMP
mechanical commissioning
automation commissioning
Factory Acceptance Testing
user manuals
Quality Management Systems
Job Description
Company:
Job Description:
The Engineering Intern will assist with the specification, design, manufacture, documentation, and qualification of custom and standard capital equipment used for pharmaceutical and biopharmaceutical product manufacturing (example equipment types include chromatography, buffer formulation, virus filtration, oligonucleotide synthesis):
assist project team during any project-related activities
interface as appropriate with vendors
interface as appropriate with customer stakeholders
assist with equipment assembly
assist with commissioning and validating assembled equipment
manage variety of concurrent assignments
apply curious, energetic, and customer-focused mindset
make suggestions for improvement as applicable
Primary Duties and Responsibilities
Customer Projects:
Create and / or review design documents, including technical drawings and specification documents
Create and / or review detailed project-specific test protocols in accordance with GAMP and established templates and practices
Execute testing activities including mechanical and automation commissioning, GAMP qualification, and Factory Acceptance Testing
Construct user manuals and other customer-facing documents to comply with project requirements and realize customer satisfaction, and perform engineering review of final documentation turnover packages
Internal Projects:
Research technology, components, companies, or solutions for specific internal projects
Contribute to process improvement activities as directed
Additional Duties and Responsibilities
Seek and participate in current, relevant technical training as well as non-technical training opportunities
Provide subject matter training to colleagues and customers
Contribute technical support to Quality for addressing customer feedback and supplier issues
Minimum Requirements
Currently in pursuit of Bachelor’s or Master’s Degree in Engineering (Mechanical, Chemical, Electrical, Biomedical)
Ability to work onsite at Glenview facility
Awareness of Quality Management Systems
Awareness of personal strengths, weaknesses, and impact of decisions on wider team and department
Eagerness to learn new technical information, new processes, and new skills
Willingness to assist outside of everyday responsibilities when required
Possess these qualities: energetic, positive, strong interpersonal communicator, detail-oriented, ethics-minded, problem-solver, adaptable, team-oriented, customer-focused, and self-motivated
Physical Demands and Environmental Conditions
Occasional exposure to pressurized liquids, live electrical circuits, and/or chemical solutions requiring proper personal protective equipment (provided)
The base compensation range for this role is $18-20/hour. Base Compensation is influenced by many factors including, but not limited to: time in the role, previous experience, skills, knowledge, performance, work requirements, internal equity, and business / economic conditions.
About Asahi Kasei Bioprocess America, Inc.
Asahi Kasei Bioprocess America, Inc. (AKBA) provides pharmaceutical and biopharmaceutical manufacturers with a comprehensive suite of tools to maximize safety and improve yields of biotherapeutics during research, clinical and commercial-scale production. Planova™ virus-removal filters anchor a diverse product portfolio defined by quality, consistency and scalability. Additional areas of expertise include liquid chromatography, inline buffer dilution and oligonucleotide synthesis.
We are a growing team (140+) of professionals excited about what we do and our ability to impact healthcare delivery systems worldwide. We offer a "big company" benefits package and a "small company" culture and work environment. Every employee at Asahi Kasei Bioprocess America can impact our future.
Please note, we will not be providing immigration-related sponsorship now or in the future for this role.
#LI-SG1
As an equal opportunity employer, Asahi Kasei believes a diverse workforce will provide us with the ability to continuously support the changes in the economy, society, and environment.
Asahi Kasei
🏢 About Asahi Kasei The Asahi Kasei Group contributes to life and living for people around the world. Since its foundation in 1922 with ammonia and cellulose fiber business, Asahi Kasei has consistently grown through the proactive transformation of its business portfolio to meet the evolving needs of every age. With more than 50,000 employees around the world, the company contributes to sustainable society by providing solutions to the world’s challenges through its three business sectors of Health Care, Homes, and Material. ⚠️Be cautious of fraudulent communications claiming to be from Asahi Kasei. If someone does not have a verification badge, that person is not authorized to engage in recruitment activities on behalf of Asahi Kasei.
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