GMP Microbiology Quality Lab Associate I

Doist; Bloomington (IN); On-site; USD 42,000 - 64,000; Full time

Benefits offered by this job

Medical & Dental Coverage

401(k) Retirement Savings Plan with a

Paid Time Off

Education Assistance Program

Onsite Campus Amenities

Employee Assistance Program

Job summary

The Microbiology Quality Lab Associate I at Simtra BioPharma Solutions in Bloomington, IN performs complex routine and non-routine sampling and processes samples to support the Microbiology department. This role reports to a Microbiology Supervisor.

You will conduct testing (bioburden, sterility, growth promotion) on finished products and in-process samples, document results in LIMS, and participate in continuous improvement activities in a GMP-regulated environment.

Qualifications

• Bachelor’s degree in a science-related field, preferably Microbiology.
• Previous GMP-regulated environment experience is preferred.
• Computer proficiency: Word, Excel, Outlook; ability to use enterprise software (JDE, BPLM, Pilgrim, Trackwise, etc.).

Responsibilities

• Perform testing (bioburden, sterility, growth promotion, etc.) on finished products and in-process samples.
• Conduct investigational work for out-of-specification samples to identify root causes and corrective actions.
• Document and process samples in a Laboratory Information Management System (LIMS).
• Investigate and author Microbiology investigations.
• Enter test data into LIMS and participate in continuous improvement activities.

Skills

Bioburden testing

Sterility testing

Growth promotion testing

Documentation in LIMS

Continuous improvement

Education

Bachelor's degree in science (preferred Microbiology)

Tools

Microsoft Word

Excel

Outlook

JDE

BPLM

Pilgrim

Trackwise

Job description

The Microbiology Quality Lab Associate I at Simtra BioPharma Solutions in Bloomington, IN performs complex routine and non-routine sampling and processes samples to support the Microbiology department. This role reports to a Microbiology Supervisor.

You will conduct testing (bioburden, sterility, growth promotion) on finished products and in-process samples, document results in LIMS, and participate in continuous improvement activities in a GMP-regulated environment.