QA - In Process Inspector - Second Shift

Inteplast Group; Town of Florida, Northern (NY, KY); Hybrid; USD 50,000 - 65,000; Full time

Job summary

Inteplast Group's Florida facility is seeking an In Process Inspector B for the second shift (Mon-Fri, 3:00PM–11:30PM) to execute quality control sampling throughout manufacturing, production and packaging, ensuring compliance with product specs, cGMPs and safety procedures.

You will prepare detailed reports, communicate findings to QC personnel, support audits, and maintain accurate data recording across processes to prevent non-conformities.

Qualifications

• High School Diploma or equivalent with 1–2 years in QA/quality control.
• Knowledge of sampling and testing techniques in manufacturing.
• Good math skills and attention to detail.
• Ability to work with cGMPs, SOPs, and safety procedures.
• Excellent written and verbal communication.

Responsibilities

• Perform QA sampling, testing, and record data accurately.
• Communicate results and data to QC personnel and supervisor.
• Maintain quality standards throughout manufacturing and packaging.
• Adhere to cGMPs, SOPs, MSDS, and safety rules.
• Assist with audits and data validation as needed.

Skills

Attention to detail

Written and oral communication

Ability to manage stress

Punctual attendance

Education

High School Diploma/Certificate

Job description

QA - In Process Inspector - Second Shift

Job Description

Mon - Fri

3:00PM - 11:30PM

TITLE: In Process Inspector B

POSITION OBJECTIVE: Responsible for performing all Quality Control and Assurance sampling functions throughout the entire process of manufacturing, production and packaging, by product specification, following cGMP's and Standard Operation Processors, food safety regulations, and safety procedures.

QUALIFICATIONS:

• Ensure consistent, dependable attendance and demonstrate a willingness to accommodate non-standard work hours as necessary.
• Capable of effectively managing job-related stress and fostering productive workplace interactions.
• High School Diploma/Certificate; or one to two years related experience and/or training; or equivalent combination of education and experience.
• Requires 1-2 years experience in quality assurance, quality control or related inspection activities, preferably in a nutraceutical or pharmaceutical environment.
• Basic knowledge of quality processes for manufacturing, production and packaging, including but not limited to basic knowledge of sampling techniques, sample testing techniques, systems and equipment.
• Good written and oral communication skills.
• Good mathematical skills and attention to detail.

JOB RESPONSIBILITIES:

• Communicate regularly with QC personnel and Supervisor/Manager, provide detailed reports, testing results, sample analysis and OOS items, quality issues and findings, in order to approve processes and to identify and correct issues immediately.
• Conduct ongoing Sampling Quality Assurance inspections and prepare for audits.
• Perform sample collections, sample preparation, sample processing and sample testing to ensure consistency throughout the process, and record all data as required and instructed by supervisor.
• Maintain all required Standards of Quality throughout the entire process.
• Follow cGMP's, SOP's, MSDS specifications, Sampling Plans, Safety in the Workplace if and when applicable; adhere to safety policies and procedures at all times.
• Report any out-of-compliance items to the supervisor immediately.
• Document all results, findings, information and record data timely and accurately.
• Perform data retrieval and reporting, ensure correct usage of quality related documents, perform multiple sample quality control processes concurrently to demonstrate consistency of performance.
• Perform operational tasks as needed, requested, directed or instructed by the supervisor/manager.
• Assist with validation of data, processes and equipment, equipment preventive maintenance and operational tasks, as needed.
• Identifies any deficiencies, constrains and/or problems that could impede the efficient process flow and assist and/or provide ideas and feedback to solve them.
• May be required to perform other duties as requested, directed or assigned.

TRAINING:

• Working knowledge of Safety in the Workplace Rules and Regulations, preferred.
• Working knowledge of cGMP’s a plus.

Florida Supplement is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.