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Quality Control Analyst

Integrated Resources, Inc ( IRI )
Paul, MN Contractor
POSTED ON 3/26/2025 CLOSED ON 3/29/2025

What are the responsibilities and job description for the Quality Control Analyst position at Integrated Resources, Inc ( IRI )?

Quality Control Analyst I

Location: St. Paul, MN (onsite)

Duration: 12 months (possibility of extension)

Offered pay: $23/hr


Job Overview:

The Quality Control Analyst I is responsible for conducting biological, chemical, and physical analyses on pharmaceutical products, biologics, drugs, and medical devices across all manufacturing stages. This includes raw materials, in-process testing, finished goods, and environmental monitoring.

Key Responsibilities:

Perform critical biological, chemical, and physical testing on raw materials, in-process, and final products.

Utilize laboratory instrumentation and computer systems (e.g., LIMS) to collect and record data.

Conduct precise analytical assays requiring a strong understanding of biology and chemistry principles.

Ensure data integrity and compliance with FDA, GLP, QSR, and cGMP regulations.

Document exceptions and deviations in compliance reports.

Participate in process improvement efforts to enhance quality, efficiency, and cost savings.

Conduct laboratory and manufacturing audits and update SOPs as required.

Perform equipment maintenance and calibration as needed.


Qualifications & Skills:

Bachelor’s degree in Chemistry, Biological Sciences, or related field (with coursework in Analytical Chemistry or Laboratory Techniques).

0-2 years of relevant experience in quality control, pharmaceutical, or laboratory settings.

Strong attention to detail and ability to manage multiple tasks efficiently.

Basic knowledge of laboratory instrumentation and pharmaceutical production equipment.


Preferred Experience:

Experience with LIMS, autoclaves, incubators, CIP/SIP systems, and analytical equipment.

Prior work in pharmaceutical or biotech manufacturing settings.

Knowledge of chemical and biological safety protocols.

Understanding of cGMP, GLP, and quality standards in a regulated environment.

Proficiency in computer systems for data entry, training, and documentation.

Excellent written and verbal communication skills for reporting and team collaboration.

Ability to follow detailed instructions and adhere to safety procedures.

Personal attributes: Integrity, accountability, problem-solving mindset, eagerness to learn, and dedication to quality.

Salary : $23

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