Description

The Manufacturing Associate I (Aseptic) will play a crucial role in the daily operations of our manufacturing facility. You will be involved in various tasks including weighing and dispensing materials, operating equipment, and participating in drug substance manufacturing processes. This position requires adherence to strict aseptic practices while ensuring compliance with safety and cGMP regulations.

Company Culture and Environment

Our company fosters a culture of safety, quality, and continuous improvement. Teamwork and collaboration are emphasized as associates support each other in maintaining high standards in a cleanroom environment.

Career Growth and Development Opportunities

As a Manufacturing Associate I, you will have opportunities to develop your skills in aseptic manufacturing and participate in the training of new employees. There is potential for career advancement within the manufacturing team as you gain experience and expertise in cGMP processes.

Detailed Benefits and Perks

While specific benefits are not listed in the job description, the role provides valuable hands-on experience in a regulated environment, which can serve as a strong foundation for your career in the pharmaceutical manufacturing industry.

Compensation and Benefits

• Competitive hourly wage based on experience
• Opportunities for overtime
• Professional training and development

Why you should apply for this position today

This is an excellent opportunity for individuals looking to start or advance their career in pharmaceutical manufacturing. You will gain essential skills in aseptic processing and cGMP compliance, making you a valuable asset in the healthcare industry.

Skills

• Strong attention to detail
• Ability to follow strict aseptic and safety protocols
• Basic knowledge of cGMP regulations
• Good communication skills
• Team-oriented mindset
• Willingness to learn and adapt

Responsibilities

• Weighing and dispensing materials
• Operating Glasswasher and autoclave
• Preparing media and buffers
• Participating in drug substance manufacturing and filtration systems
• Performing aseptic filling of glass vials and pre-fillable syringes
• Conducting visual inspections of glass vials and prefilled syringes
• Training in aseptic practices in the ISO 6 area
• Participating in media fill operations
• Handling secondary packaging, material issuance, and visual inspection
• Conducting in-process testing (pH, conductivity, etc.)
• Verifying raw materials and commodities
• Completing Batch Records and other cGMP documentation accurately and timely
• Disposing of soiled materials appropriately
• Maintaining cleanroom standards
• Reporting nonconformance to the Supervisor
• Complying with safety and company policies
• Writing and reviewing cGMP documentation like SOPs and Batch Records
• Assisting with new employee training
• Supporting coordination of activities as necessary

Qualifications

• High school diploma or equivalent
• Experience in a regulated environment is a plus
• Knowledge of pharmaceutical manufacturing is desirable

Education Requirements

• High School Diploma or equivalent required

Education Requirements Credential Category

• High School Diploma or equivalent

Experience Requirements

• Previous experience in a manufacturing or laboratory environment preferred but not mandatory
• Familiarity with cGMP processes is an advantage

Why work in Chicago, IL

Chicago offers a vibrant urban environment with a rich history, diverse culture, and numerous professional opportunities. The city is known for its thriving healthcare and biotechnology sectors, making it an ideal location for career growth in the life sciences field. With its wide array of dining, entertainment, and cultural events, Chicago provides a well-rounded lifestyle for residents.