Description

The Manufacturing Associate I is a full-time, non-exempt position responsible for the manufacturing of Biotechnology products for clinical and commercial human use. In this role, you will employ aseptic techniques while working in controlled and classified environments, adhering to SOPs, FDA current Good Manufacturing Practices (cGMP), and any other governmental requirements.

Company Culture and Environment

The workplace emphasizes safety and adherence to strict guidelines, promoting a culture of compliance and teamwork. Employees are expected to operate independently while also collaborating effectively with others in a dynamic environment.

Career Growth and Development Opportunities

This position offers opportunities for professional development through hands-on experience in biotechnology and the potential for technology transfer from Process Development to cGMP Manufacturing.

Detailed Benefits and Perks

• Flexible working hours, including rotating shifts
• Opportunities for skill enhancement in biotechnological processes
• A structured training environment to improve compliance and technical skills

Compensation and Benefits

• Competitive salary based on experience
• Health, dental, and vision insurance
• Retirement savings plan options
• Paid time off and holidays

Why you should apply for this position today

This role is an excellent opportunity for individuals looking to grow their careers in the biotechnology field while making a tangible impact on human health. You will gain valuable experience in a cleanroom environment and be part of a dedicated team focused on advancing biotechnology products.

Skills

• Basic verbal and written communication skills in English
• Excellent interpersonal skills
• Ability to operate complex systems and equipment
• Basic troubleshooting skills for equipment and processes
• Proficient in word processing, spreadsheets, and data management
• Knowledge of GMP and safety requirements
• Familiarity with biotechnology operations, including Aseptic Filtration Systems and Chromatography Columns

Responsibilities

• Weighing and dispensing of materials
• Operating filtration systems
• Inoculating mammalian or cytokine cells
• Conducting fermentation and harvest processes
• Managing chromatography columns and TFF operations
• Performing in-process testing (e.g., pH, conductivity, spectrophotometer)
• Preparing media and buffer solutions
• Completing Batch Records and cGMP documentation promptly
• Maintaining cleanroom conditions and disposing of soiled materials
• Reporting nonconformances to the Supervisor
• Assisting in technology transfer from Process Development to cGMP Manufacturing
• Following all safety, cGMP, and company policies

Qualifications

• Basic understanding of technical documents and procedures
• Ability to follow detailed directions reliably
• Strong problem-solving skills and ability to work independently or as part of a team

Education Requirements

• Associate degree or higher in Biology, Chemistry, Biotechnology, or a related field preferred
• Or 1-2 years of biologics industry experience

Education Requirements Credential Category

• Associate’s Degree or higher preferred

Experience Requirements

• 1-2 years of experience in the biologics industry required

Why work in Chicago, IL

Chicago is a vibrant city known for its rich history, diverse culture, and booming job market. With numerous biotech firms and academic institutions, the city provides a supportive environment for professional growth and networking. Enjoy a dynamic lifestyle with access to world-class dining, arts, and entertainment.