Supervisor, Quality Assurance

Leiner Health Products

America’s largest store brand manufacturer of vitamins, minerals, supplements (VMS) and diet aids and leading producer of store brand over the counter (OTC) pharmaceuticals, is searching for a dynamic Quality Assurance Supervisor for our Garden Grove location.

 

For the Opportunity of Your Life...Come Join Our Team!

 

Leiner Employees Enjoy (Garden Grove):Fitness CenterBusiness Casual EnvironmentProduct Purchase Program (discount rates)Employee Store with over 90+ vitamin/health products itemsAdvantage Club (discount cards to recreation and theme parks)

We offer the following benefits:

Medical, Dental, Vision, Life, 401K, Employee Assistance Program,

Educational Assistance, and Paid Holidays.



 

The Supervisor is responsible for supervising the approval or rejection of components, raw materials, labeling, in-process material, and finished products.  Responsibilities also include:

 Review production records to assure material meets specifications.Investigate and document errors which occur during production.  Ensure adherence with cGMPs, SOPs, state and local regulations, in addition to customer specific requirements.Operational –Supervises the required Material Resource Planning (MRP) transactions for approvals, releases, quarantines, and rejections.  Ensures that work center inspection and in-process checks are properly performed.  Conducts and/or assists in investigations concerning operational problems and/or problems involving customer complaints.Departmental/Shift Administration – Schedules the work assignments for the department/shift.  Sets challenging yet achievable goals for staff.  Helps staff to build upon their capabilities and encourages others to achieve results.  Responsible for the training and motivation of the department. Maintains open lines of communications with department.  Provides input into department budget.  Conducts performance evaluations with the assistance of department management.  Stays abreast of developments in the field through own study as well as attendance of various seminars and workshops.  Recommends objectives and department goals.  Functional Administration – Conducts perpetual plant audits for strict adherence to cGMPs and SOPs.  Assists with the training of plant personnel in cGMPs.  Helps to develop SOPs.  Oversees the maintenance of the retain sample program, environmental monitoring, and settling plate (micro) monitoring programs.Continuously reviews efficiency opportunities within the daily workflow and recognizes the need for new or modified work procedures.  Seeks out and uses new tools, processes, and procedures to add value to the company.  Anticipates issues and works proactively to resolve problems.May be required to handle hazardous waste.  Performs other related duties as assigned by management.  Some travel required, such as vendor audits, seminars, and site visits.

Successful candidates for this position will possess:

 Bachelor’s Degree in a Life or Physical Science is required.  Must have a working knowledge of cGMP and regulatory guidelines.PC and mainframe literacy required.   Must effectively communicate cross functionally with peers, associates, and upper level management.  Able to write and ensure technical content is correct.  Good verbal and written communication skills required.  Ability to work independently and in a team environment.  Understands goal measurements.  Creates a goal oriented climate in the work force.  Ability to effectively interact in group.  Ability to display and reach concession.  Ability to take on team leader roles.ASQ – CQA preferred.

 

NO THIRD-PARTY RECRUITERS.