Description

The Manufacturing Associate I is a full-time non-exempt position located in Chicago, IL, wherein the employee will engage in the manufacturing of Biotechnology products for clinical and commercial human use. This role requires the application of aseptic techniques while working in controlled and classified environments, necessitating complete aseptic gowning. Compliance with Client policies, procedures (SOP), FDA current Good Manufacturing Practices (cGMP), and other government requirements is mandatory.

Company Culture and Environment

The work environment emphasizes adherence to safety and quality standards, promoting a culture of accountability and teamwork. Employees are encouraged to follow detailed directions while contributing to the overall efficiency and cleanliness of the manufacturing space.

Career Growth and Development Opportunities

The role provides opportunities for employees to grow within the biotechnology field, especially through hands-on experience in drug manufacturing processes and technology transfer from Process Development to cGMP Manufacturing.

Detailed Benefits and Perks

While specific additional perks are not outlined, working in a biotechnology environment often includes standard benefits such as health insurance and opportunities for continuous learning and development in the field.

Compensation and Benefits

• Competitive salary based on experience
• Health and wellness programs
• Opportunities for professional development

Why you should apply for this position today

This position offers the chance to work at the forefront of biotechnology, contributing to products that have a significant human impact. Ideal candidates who are eager to follow safety protocols and thrive in a team-oriented environment will find this an excellent opportunity.

Skills

• Basic verbal and written communication skills in English
• Excellent interpersonal skills
• Ability to operate complex systems and equipment in alignment with current GMPs and SOPs
• Problem identification and troubleshooting skills
• Proficiency in word processing, spreadsheets, and data management
• Knowledge of GMP and safety requirements
• Understanding of biotechnology operations such as aseptic filtration systems, fermentation processes, and chromatography columns

Responsibilities

• Engage in daily operations including weighing and dispensing materials
• Operate filtration systems and inoculate mammalian or cytokine cells
• Participate in fermentation and harvest processes
• Work with chromatography columns and TFF operations
• Execute in-process testing (pH, conductivity, spectrophotometer, etc.)
• Prepare media and buffer solutions
• Complete Batch Records and other cGMP documentation accurately and timely
• Maintain cleanroom manufacturing conditions
• Report nonconformance events to the Supervisor
• Assist in technology transfer from Process Development to manufacturing
• Comply with safety and company policies and procedures

Qualifications

• Drug manufacturing experience required
• Associate degree or higher in Biology, Chemistry, Biotechnology, or related field preferred
• 1–2 years of biologics industry experience required

Education Requirements

• Associate degree or higher in a relevant field

Education Requirements Credential Category

• Degree in Biology, Chemistry, Biotechnology, or related field preferred

Experience Requirements

• Equivalent of 1–2 years of biologics industry experience required

Why work in Chicago, IL

Chicago is a vibrant city known for its rich history, diverse culture, and strong presence in the biotechnology sector. The city provides numerous opportunities for networking, professional development, and a high quality of life with a variety of recreational activities, dining options, and cultural experiences.