Description

The Microbiology Analyst I is a full-time exempt position based in Chicago, IL, responsible for supporting the Microbiology and Environmental Monitoring (EM) department. This role involves implementing and managing microbiology and EM programs as well as overseeing laboratory operations to ensure compliance with current regulations. The position requires direct interaction with biological non-sterile drug substance and sterile drug product manufacturing processes, with a requirement for aseptic gowning qualifications.

Company Culture and Environment

The company fosters a collaborative and compliant work environment, emphasizing adherence to current regulations and meticulous attention to detail. Employees are expected to effectively manage their time and contribute to both individual and team goals, highlighting a strong organizational culture.

Career Growth and Development Opportunities

While specific career growth opportunities are not detailed in the job description, the position in a cGMP pharmaceutical manufacturing environment may provide valuable experience and skills that could facilitate professional advancement within the industry.

Detailed Benefits and Perks

The job description does not specify particular benefits or perks beyond the standard expectations for a full-time position in the pharmaceutical industry.

Compensation and Benefits

• Competitive salary based on experience
• Full-time exempt position
• Opportunities for professional development

Why you should apply for this position today

This role offers a unique opportunity to contribute to critical microbiology and EM programs within a reputable pharmaceutical environment. Candidates will gain valuable experience working with aseptic and non-sterile manufacturing processes, which are essential for career advancement in the industry.

Skills

• Good written and verbal communication skills
• Strong organizational skills
• Detail-oriented
• Effective time management abilities
• Proficient with Microsoft Excel and Microsoft Word

Responsibilities

• Perform environmental monitoring of controlled and aseptic manufacturing areas
• Collect samples for detecting viable and non-viable particles
• Incubate viable samples and manage sample tracking
• Conduct tests for bacterial endotoxin, bioburden, and microbial limits
• Perform sanitation and temperature verification of laboratory equipment
• Monitor water systems and submit samples for testing
• Maintain accurate data entry for trend analysis
• Other tasks as assigned by management

Qualifications

• Bachelor’s degree in microbiology, biology, or a related discipline
• Some experience in a cGMP pharmaceutical manufacturing environment preferred

Education Requirements

• Bachelor’s degree in microbiology, biology, or a related discipline

Education Requirements Credential Category

• Bachelor’s degree

Experience Requirements

• Some experience in a cGMP pharmaceutical manufacturing environment is preferred

Why work in Chicago, IL

Chicago offers a vibrant urban environment with a rich cultural scene, diverse entertainment options, and a strong professional community in the pharmaceutical and biotechnology sectors. The city provides a dynamic backdrop for both personal and professional growth, making it an attractive place to live and work.