Who we are:

Charter Medical, LLC is a life sciences company that is committed to designing, developing, and manufacturing quality products to support cell and gene therapy, bioprocessing, and blood management.

About the role:

The Quality Control Technician conducts inspection and testing activities at various manufacturing stages including incoming, in-process, and final release.

3rd shift: Sunday-Thursday 11:00 pm-7:00 am

What you will do:

• Performs in-process and final inspections; including visual, dimensional and functional verifications, as well as inspections for defects, non-conformance and contamination with adherence to Work Instructions (WI’s), Visual Inspection Criteria, Standard Operating Procedure (SOP) and internal specifications defined for each product.
• Records inspection results and completes appropriate documentation; assists notification of non-conforming product/processes.
• Follows documented procedures to maintain control of non-conforming products by identifying and segregating products that do not meet specifications and completing appropriate documentation.
• Performs Quality Control (QC) verification of line openings, closing and subsequent line clearances. Records sample collection in current Enterprise Resource Planning (ERP) system.
• Performs verification or calibration of measurement equipment.
• Ensures proper labeling of acceptable material.
• Reviews supplier certifications/packing list to ensure compliance with specification.
• Assists in collection of data for certification of finished products.
• Logs, files, and maintains finished goods retention samples.
• Assists with receiving inspection of raw materials using appropriate sampling plan and measuring/test equipment as needed.
• Assist in all areas within the quality department as needed.

Who you are:

• High school graduate or equivalent required.
• Two years Quality experience preferred.
• Ability to effectively communicate with coworkers and management. Business communication is conducted in English.

• Ability to comprehend and follow SOP’s, WI’s, policies, and procedures such a safety, quality, and HR that are written in English.
• Possess basic mathematical skills to add, subtract, multiply and divide in all units of measure, using whole numbers, common fractions, and decimals.
• Basic understanding of GMP and working within FDA regulated industries preferred.
• Basic computer skills including ability to use MS Outlook and automated manufacturing and quality systems.
• Excellent interpersonal skills with ability to get along well with others and work in a team environment.
• Ability to properly complete paperwork as required according to work instructions, standards, or other specifications.
• Excellent dependability and reliability.
• Willingness to accept change, learn, and work with new processes.
• Familiarity with an ERP system and Quality Management System (eQMS) preferred.

• Must be able to work extended hours when required.

• 20/20 vision (with corrective eyeglasses) and ability to pass a color perception test.

Perks / Benefits:

• Generous Paid Time Off
• Paid Breaks
• Annual Bonuses
• 401k with excellent company match
• Health Insurance with multiple plans to choose form
• Paid Short Term and Long Term Disability