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Inteplast Group

6102 - FS QC - IPRB - In Process Inspector B

Inteplast Group, Miramar, Florida, United States

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6102 - FS QC - IPRB - In Process Inspector B

Job Description

Posted Monday, June 23, 2025 at 4:00 AM | Expires Saturday, July 5, 2025 at 3:59 AM Mon - Fri 3:30PM - 12:00AM 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 cGMPs and Standard Operating Procedures, 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 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 cGMPs, SOPs, 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 performance consistency. 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. Identify any deficiencies, constraints, 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 cGMPs 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.

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