Quality Control Manager Phoenix Arizona

Quality Control Manager Phoenix Arizona
Company:

Eiworkflow Solutions, Llc


Place:

Arizona


Quality Control Manager Phoenix Arizona

Details of the offer

eiWorkflow Solutions, LLC is a consulting firm based in Albany, NY. eiWorkflow Solutions, LLC is currently looking for a consultant for the following role.

Quality Control Manager Phoenix Arizona

Tasks the role will be performing:
The Quality Control Manager is responsible for the quality control functions within the all company facilities. The QC Manager verifies product quality and is responsible for specific quality assurance documentation and data gathering. The QC Manager will supervise and monitor the inspection and testing of materials, parts, and products to ensure adherence to established quality standards. The QC Manager also establishes inspection protocols, defines sampling procedures, determines equipment and mechanisms to be used in the testing process, and may suggest improvements to process, revise quality control policies and procedures, as well as be a knowledge resource for other team members. In this role, the QC Manager will report to the Plant Manager any issues that need to be addressed.

Requirements for the position:
• Leads, trains, and coaches QC staff to ensure manufacturing requirements are met;
• Act as department communicator during status meetings, management updates, and staff shift changes;
• Ensure products are in compliance with professional standards and customer requirements;
• Stays up-to-date with CGMPs, FDA, NSF and other regulatory guidelines;
• Signs off on verifications, packets, logs, and other documentations;
• Approves incoming materials by confirming specifications; laboratory testing, conducting visual, organoleptic and measurement tests; rejecting and returning unacceptable materials;
• Responsible for creating C of A’s for internal test results as well as releasing C of A’s from 3rd party laboratories;
• Writing and finalizing Master Manufacturing Record (MMR’s);
• Collaborating with R&D personnel to document and finalize future products and processes;
• Responsible for administering the company quality control program in accordance with customer and company requirements;
• Determine, establish and enforce, through all operational departments, quality and safety requirements in accordance with company needs, based on FDA regulations, cGMP, NOP(National Organic Program), and other regulatory guidelines;
• Act as liaison with external parties on matters relating to the quality system and support all operational departments;
• Participate in organizational committees, such as Osha Safety, Hazard control, Formula change;
• Recommends changes in specifications of materials, parts, and products based on inspection results;
• Help develop in-house training material related to regulatory statutes;
• Responsible for the training of personnel in cGMPs and overseeing audits;
• Oversees audits and/or quality regulatory inspections;
• Assure that all documentation is maintained, updated, reviewed and approved to reflect current processes;
• Assure that all consumer complaints are recorded properly and are closed out upon resolution;
• Assure all components and raw materials meet specifications for use in processing of intermediate and final product by documented methods of sampling, testing, formulation, labeling, storage, distribution, and approvals;
• Assure that all process errors, product failures and any process deviations are investigated and that any corrective actions and/or preventive actions are carried out;
• Responsible for creating CAPA’s and participating in root cause investigation;
• Help develop laboratory necessities and/or research laboratory equipment;
• Perform other related duties as assigned by Plant Manager.

Requirements

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