Director of Quality Control - Regulatory Affairs

Market America•Greensboro, NC

3d•Onsite

About The Position

Market America, a Global Product Brokerage and Internet Marketing company, is seeking a Director of Quality Control & Regulatory Affairs. This role will manage the overall operations of the Quality and Regulatory Department to ensure goals are met effectively and efficiently. The Director will also direct and supervise lead and managerial staff within the department. This position is on-site in Greensboro, NC.

Requirements

10+ years of experience in Quality Control, Pharmaceutical, Science Operations, and staff supervision.

Nice To Haves

PHD in Chemistry, or related field preferred

Responsibilities

Serves as Senior Staff member of the Quality Assurance and Regulatory Affairs team to support, educate, motivate and direct the team.
Ensures a clear understanding of duties, provides accountability for performance and helps maximize high pay off activities that will increase productivity and profitability of product lines.
Responsible for the systems and processes implemented to ensure compliance to Good Manufacturing Practices; compliance with State, Federal and International regulatory standards; and the quality standards of our vendors.
Maintains accountability to the direction provided by the Executive Vice President and Vice President of Product Management.
Anticipates, evaluates and controls risks associated with complying with industry and government regulations.
Ensures timely completion of projects assigned to the team.
Predicts, detects, estimates, and measures product defects.
Oversees labeling changes in compliance with government regulations, including allergen labeling, ingredient, warnings and nutrient content labeling.
Develops, implements, and trains on departmental policies and procedures that impact job performance.
Determines areas for improvement and quality.
Collaborates with other departments to ensure all parties have the required information for success in their roles.
Manages the Quality Control Department to provide any needed information such as label review, vendor issues, and manufacturing changes.
Ensures that all products (drugs, dietary supplements, cosmetics, skin care) are manufactured, tested, stored, and distributed according to Good Manufacturing Practices (cGMP) and other applicable regulations and specifications.
Complies with Company policies and procedures.
Performs other duties as assigned.