6102 - FS QC - IPRB - In Process Inspector B

Inteplast Group•Miramar, FL

2d•Onsite

About The Position

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.

Requirements

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.
Computer literacy (M.S. Word & Excel).

Nice To Haves

Associate degree in related science education, preferred.
Working knowledge of Safety in the Workplace Rules and Regulations, preferred.
Working knowledge of cGMP’s a plus.

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.