Supervisor, Quality Control

Leiner Health Product

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 Supervisor of Quality Control for our Garden Grove location.

 

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

 

Leiner Employees Enjoy (Carson Facility):On-Site Fitness CenterProduct Purchase Program (discount rates)Employee Store with over 90+ vitamin/health products itemsOn-Site Car Wash every WednesdayBusiness Casual EnvironmentAdvantage 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 and training all laboratory personnel (up to 40 direct reports), directing the flow of the laboratory operation and testing product samples for release of product.  Responsibilities also include:  Establish and enforce procedures and policies to ensure completion of appropriate testing and documentation according to company policy, cGMPs, GLPs, and regulatory requirements. Administer incoming raw materials, in-process and finished products through communication with Technical Operations, R&D, QA, Purchasing, Production & Inventory Control, and Regulatory AffairsWrite, review and/or revise all departmental Standard Operating Procedures (SOPs) and test procedures, including assay methods development and validation and ensure compliance. Participate in the establishment of uniform corporate laboratory procedures. Write, review, and approve product specifications on raw material, purchased products, in-process and finished products.  Produce written reports of special projects as needed.  Provide training, supervision and technical guidance to all laboratory employees including safety.Coordinate samples and paperwork for all samples.  Review data as testing is completed, for raw material, in-process and finished bulk product including buy-out and stability samples, process alert forms and initiate investigation procedures, if needed. Conduct LIRs (Laboratory Investigation Reports).Review and approve outgoing Certificate of Analysis and corporate stability reports. Coordinate Customer Complaint investigation, product testing (in-house and outside lab testing) on Competitors’ samples, Marketing New Product samples, R&D and Process Engineering pilot samples.

Successful candidates for this position will possess:Bachelor’s degree in Chemistry or related field required.  Master’s degree preferred.Minimum 5 years'  analytical laboratory experience,  with min. 1 year in a lead role. Previous supervisory exp. Pharmaceutical manufacturing a plus. Familiar with cGMPs and Good Laboratory Practices (GLP).Strong written/verbal communication, math, computer and organizational skills required. Knowledge of specific regulatory requirements related to pharmaceutical QC testing required.  Good supervisory and training skills required.

 

NO THIRD-PARTY RECRUITERS.