Mq Inspector I - 3Rd Shift (395)

NOW Health Group•Bloomingdale, IL

4d•Onsite

About The Position

The Mq Inspector I is responsible for performing quality control inspections on raw materials, in-process materials, and finished products to ensure compliance with Good Manufacturing Practices (GMPs) and Standard Operating Procedures (SOPs). This role involves detailed documentation, testing, and communication with various departments to maintain product quality and safety. The inspector will work in a manufacturing environment and must adhere to all safety regulations.

Requirements

High school diploma or equivalent.
Zero to two years related inspection experience.
Familiarity with general inspection procedures.
Basic computer skills.
Ability to read and interpret documents such as product specifications, departmental instructions, and procedure manuals.
Ability to write routine e-mails to communicate within QC and with operations personnel.
Good writing and good communication skills.
Ability to apply concepts such as fractions, percentages, and averages.
Ability to compare results to specifications to determine if result meets requirements.
Ability to interpret a variety of instructions.
Ability to work in a quick-paced environment and change tasks frequently.
Ability to learn quickly, operate independently, and to assume responsibility for new tasks.

Nice To Haves

Experience in a quality department preferred.

Responsibilities

Performs raw material evaluation on all incoming shipments and obtains representative lot samples.
Completes necessary documentation and Oracle entries for incoming materials.
Samples incoming raw material and incoming packaged products upon receipt in the warehouse.
Reviews COC/COA (Certificate of Conformance/Certificate of Analysis) of incoming material and/or incoming packaging component, as needed.
Reviews documentation for completeness and compliance with GMPs and SOPs for processing or packaging inspection.
Performs random in-process testing to verify operator’s results.
Releases materials for use and reviews documentation for completeness.
Communicates problems/out-of-specification issues to supervisor/lead and operations personnel.
Assists supervisor/lead in conducting investigations.
Performs AQL (Acceptable Quality Limit) inspections on bulk or packaged product, as needed.
Places product on hold status to investigate quality issues.
Complies with safety and GMP requirements.
Supports a culture of safe production and operations; follows all safety rules and procedures.
Actively participates in the safety program by engaging in training, reporting safety concerns, submitting suggestions, and correcting or reporting hazards.
Assists with communicating safety information to new employees.
Fulfills responsibilities as outlined in the company safety management plan.