3rd shift Quality Technician I (Sunday-Thursday 11:00 pm-7:00 am)

Solesis•Winston-Salem, NC

7h•Onsite

About The Position

Charter Medical, part of the Solesis family of companies, specializes in single-use solutions that enable life sciences innovators to turn bold ideas into lasting breakthroughs, supporting industry-leading companies in bringing life-saving therapies to market. Operating in North Carolina, Charter Medical employs more than 150 team members across two facilities in Winston-Salem. Guided by a commitment to quality, innovation and customer success, Charter partners with customers to transform promising therapies into commercial realities. Employees contribute to solutions that support life-changing treatments and make a meaningful impact on patients around the world. This role is for the 3rd shift, Sunday-Thursday, 11:00 pm-7:00 am. The Quality Control Technician conducts inspection and testing activities at various manufacturing stages including incoming, in-process, and final release.

Requirements

High school graduate or equivalent required.
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 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.
Must be able to work extended hours when required.
20/20 vision (with corrective eyeglasses) and ability to pass a color perception test.

Nice To Haves

Two years Quality experience preferred.
Basic understanding of GMP and working within FDA regulated industries preferred.
Familiarity with an ERP system and Quality Management System (eQMS) preferred.

Responsibilities

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.