Quality Control Inspector Lead (Production)Qcip

Swiss American CDMO; Carrollton (TX); On-site; USD 65,000 - 90,000; Full time

Job summary

Swiss American Products in Carrollton, TX seeks a Quality Control Inspector Lead Production (QCIP) to assure product conformity with regulatory and quality specs under supervision. You will assign shifts, document checks, and report quality issues to supervision.

Role requires 3–5 years in a QC role within regulated environments, strong communication, leadership, and SAP proficiency, with a focus on detail and collaboration.

Qualifications

• High School Diploma or equivalent required.
• Associate’s degree in quality control, science, or engineering preferred.
• 3–5 years of experience in a regulated quality control role (FDA/USDA).
• Excellent verbal and written communication skills.
• Ability to clearly communicate complex technical information.
• Ability to resolve interpersonal conflicts within the QC Inspector group.
• Strong understanding of math concepts, fractions, percentages, ratios and proportions.
• Familiarity with rounding rules and significant figures.
• Strong analytical and problem-solving skills.
• Ability to interpret and apply SAP protocols to production processes.
• Sound decision-making to ensure product quality and safety.
• Identify and resolve quality issues promptly and effectively.
• Proficiency in Microsoft Office Suite (Word, Excel, Outlook).
• Familiarity with relevant quality control software and databases.
• Strong leadership and mentorship skills.
• Excellent organizational and time management skills.
• Ability to work independently and as part of a team.
• Strong attention to detail and accuracy.

Responsibilities

• Perform pre-production line inspections to ensure lines are clear of materials from previous runs and ready for use.
• Provide line assignments to all QC inspectors on his/her shift.
• Complete routine production line checks to document fill weights, visual conformity, and seal inspection.
• Collect, document and prepare samples for shipment for microbial and chemical testing.
• Ensure operations in production areas follow SAP SOPs and FDA/GMP guidelines.
• Assist in product/process validation activities.
• Collect and analyze samples for release testing of finished goods and bulk products.
• Monitor production floor to assure adherence to SAP SOPs and FDA/GMP regulations.
• Participate in investigations for deviations and quality failures and implement CAPAs.
• Provide a daily shift summary of production activities and issues impacting conformity.
• Conduct final review of MBRs and ensure records are complete for document control.

Skills

Quality control

Communication

Leadership

Problem solving

Data analysis

Interpersonal conflicts

Attention to detail

Teamwork

Independence

Time management

Documentation

SAP

Microsoft Office

Education

High School Diploma

Associate's Degree in quality control/science/engineering

Tools

SAP

Microsoft Office

QA databases/ software

Job description

Job DetailsJob Location: Corporate - CARROLLTON, TX 75006Position Summary: Under supervision of the Quality Control Supervisor, the Quality Control Inspector Lead Production (QCIP) is responsible for assuring that all products produced at Swiss American Products conforms to all regulatory and quality specifications. The QCIP is also responsible for providing job assignments for his/her shift as well as reporting any quality related issues to his/her supervisor.

Essential Duties and Responsibilities

• Perform pre-production line inspections to ensure that all manufacturing lines are clear of materials from previous runs and is acceptable for use.
• Provide line assignments to all QC inspectors on his/her shift.
• Complete routine production line checks to check and accurately document finished good product for fill weights, visual conformity, and/or seal inspection
• Collect, document and prepare samples for shipment for microbial and chemical testing.
• Ensure that all operations in production areas are performed in accordance with SAP SOP’s and FDA/GMP guidelines.
• Assist in execution of product/process validation activities.
• Collect and analyze appropriate samples for the release testing of finished goods and bulk products (i.e. pH and Viscosity).
• Monitor all activity on the production floor to assure adherence to SAP SOP’s and applicable FDA/GMP regulations.
• Participate in investigations for process deviations and product quality failures and assist in implementation of corrective actions.
• Provide a daily shift summary of production activities and any issues that may contribute to the manufacture of non-conforming products.
• Conduct final review of MBR’s priority to submitting to document control for review to ensure that each record is completely and accurately filled out and all activities required by the QC department are fulfilled.
• Other duties may be assigned.

QualificationsLimits of Authority:

Interprets work situations and expectations, handles issues which conform to Company policy and past practice, and refers to extraordinary situations to the Quality Control Supervisor or Quality Control Manager for guidance when necessary.

Essential Skills and Qualifications:

• High School Diploma or equivalent required.
• Associate's Degree in a relevant field (e.g., Quality Control, Science, Engineering) preferred.
• 3-5 years of experience in a Quality Control role within a regulated environment (FDA, USDA).
• Excellent verbal and written communication skills.
• Ability to clearly and effectively communicate complex technical information.
• Ability to effectively resolve interpersonal conflicts within the QC Inspector group.
• Strong understanding of mathematical concepts, including fractions, percentages, ratios, and proportions.
• Familiarity with rounding rules and significant figures.
• Strong analytical and problem-solving skills.
• Ability to interpret and apply SAP protocols to various production processes.
• Ability to make sound decisions and take decisive action to ensure product quality and safety.
• Ability to identify and resolve quality issues promptly and effectively.
• Proficiency in Microsoft Office Suite (Word, Excel, Outlook).
• Familiarity with relevant quality control software and databases.
• Strong leadership and mentorship skills.
• Excellent organizational and time management skills.
• Ability to work independently and as part of a team.
• Strong attention to detail and accuracy.

Work Environment:

The work environment characteristics described here are representative of those an employee encounters while performing the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.The noise level in the work environment is usually moderate.

Physical Demands:

The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.

• Must be able to lift up to 50lbs on a regular basis.

The above job description is not intended to be an all-inclusive list of duties and standards of the position. Incumbents will follow any other instructions, and perform any other related duties, as assigned by their supervisor. Employees will be required to perform overtime (OT) duties as requested by their manager.