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Director of Quality - Lake Bluff, United States - Aegis Worldwide
Description
Aegis Worldwide is partnering with a Contract Manufacturing Company that is looking for a Director of Quality to join their teamSalary:
130k-160k/year base (DOE)
Responsibilities:
Manage the Quality Assurance and Quality Control teams to ensure production activities and new product development is supported as required.
Monitor quality metrics and drive continuous improvement initiatives.
Knowledge of industry regulations, standards, and guidelines related to personal care product manufacturing, ensuring compliance with FDA, EPA, and other regulatory bodies.
Implement quality assurance processes, including incoming materials inspection, in-process quality checks, and finished product testing.Work with R&D and production teams to establish product specifications, standards, and testing protocols.
Maintain strong relationships with suppliers, conducting supplier audits and evaluations to ensure adherence to quality standards.
Maintain customer relations to drive the understanding of requirements and production feasibility to ensure that the organization meets and/or exceeds the customer/compliance requirements and expectations for quality.
Manage and resolve customer complaints and concerns related to quality.Work closely with cross-functional teams including R&D, manufacturing, procurement, and logistics to resolve quality issues, mitigate risks, and drive product quality improvements.
Ensure Standard Operating Procedures (SOP's) and processes are developed and maintained to meet customer and regulatory requirements.Audit programs to ensure the facility meets current Good Manufacturing Practices (cGMP's) and customer requirements.
Ensure compliance audits of company's process manufacturing and component suppliers to determine compliance status and identify risks.
Train and mentor the quality assurance and quality control teams, ensuring a thorough understanding of quality standards, procedures, and best practices.
Qualifications:
Bachelor's degree in a relevant field such as Chemistry, Chemical Engineering, or related disciplines.
7+ years of experience in quality management
Personal care or consumer goods manufacturing industry
Minimum 5+ years' experience in regulatory affairs in an FDA-regulated environment.
Strong knowledge of regulatory requirements for personal care products, including FDA regulations, GMP, and ISO standards.
Proven track record of implementing and managing Quality Management Systems (QMS) in a manufacturing environment.
Experience leading regulatory audits and inspections, with a thorough understanding of audit processes and requirements.
If you are interested please apply today My email is if you would like to schedule a time to connect.
