Validation Managers + Specialists / Chemists / QA + QC Supvs

Leiner Health Products

We’re growing and looking for world-class team members.

At Leiner Health Products, we manufacture store brand vitamins, minerals, supplements and over-the-counter drugs for America’s top retailers.

Check us out at www.leiner.com.If any of the job postings below match your skills and abilities please let us know by clicking on APPLY NOW.

Please indicate in a cover letter which position you are applying for!

** All positions below require experience in the Pharmaceutical or Bulk Pharmaceutical Industry + experience in solid oral dosages. **
REQUIREMENTS
POSITIONS & HIGHLIGHTS



Manager of Method Validation / QC
7+ years experience
Establishes, implements and executed validation policies for assigned facilities.
Establishes, implements and executes policies and procedures for QC method development, implementation and validation for assigned facilities.
Establishes, coordinates and executes validation project plans.
Interacts with internal customers as well as FDA and external consultants.





Manager of Process Validation
7 – 10 years experience
Establishes, implements and executed validation policies for assigned facilities.
Establishes, coordinates and executes validation project plans.
Interacts with internal customers as well as FDA and external consultants.





Validations Specialist II
3 – 5 years experience
Provides documented evidence that manufacturing processes are meeting predetermined specifications.
Designs validation protocols incorporating process variables, sampling methods and acceptance criteria.
Participates on validation project teams.





Validations Specialist III
5 – 10 years experience
Responsible for coordinating, locating, tracking, organizing and verifying validation documentation for cGMP compliance.
Plans, coordinates, schedules and oversees validation projects.
Review QA systems that impact the quality of drug products.






Chemist I – Methods Development / Validation
2+ years experience
Develops, troubleshoots and validates testing methodologies by analyzing and documenting raw materials, products in-process, and finished products.
Prepares validation and testing protocols, and revises SOPs.






Chemist II, QA/QC
3 – 5 years
Inspects and analyzes samples submitted for testing including – finished products, raw materials, in-process materials, stability and validation samples.
Performs physical and analytical tests.
Follows all SOP and cGMP and lab safety procedures.






QC Supervisor
4+ years
Supervises and trains all laboratory personnel.
Directs the flow of lab operation and tests product samples for release of product.
Administers incoming raw materials, in-process and finished products through communication with Process Engineering, R&D, QA, Purchasing and Regulatory Affairs.






QA Supervisor
5+ years
Supervises the approval or rejection of components, labeling, in-process material, and finished products.
Reviews production records to assure material meets specifications.
Investigates and documents errors which occur during production.







Leiner Health Products is an Equal Opportunity Employer – EEO/AA/M/F/D/V