Inspector; QA Manufacturing - 3rd Shift (11:00PM - 7:30AM)

CONTRACT PHARMACAL CORP•Town of Smithtown, NY

9d•Onsite

About The Position

The Inspector, QA Manufacturing has the primary responsibility of ensuring product quality is maintained through all phases of manufacturing in accordance with current good manufacturing practices.

Requirements

High School or GED diploma required
Knowledge of good manufacturing practices and good documentation practices preferred.
Ability to read, write, and communicate effectively.
Self-motivated with the ability to work in fast-paced environment and handle multiple tasks simultaneously.
Excellent organizational skills with ability to focus on details.

Responsibilities

Perform in-process monitoring (e.g. weight, thickness, hardness, disintegration, friability, etc.) of all manufacturing operations
Perform duties using good documentation practices
Collect in-process and finished product samples as required
Support collection of microbiological samples per procedure as required
Perform room inspections/clearances as required
Perform Batch Record release of both Commercial and IP batch records
Perform AQL sampling and inspections as required
Identify and report any non-conformances/discrepancies to management if applicable
Review general SOPs are being met by production
Assist in employee training (initial and ongoing)
Support environmental monitoring activities (i.e. water sampling air sampling)
Provide additional QA technical support to Coating Department
Review batch record documentation
QMS form issuance as required to production
Daily scale weight verification
Maintain QA supplies
Review and approve weekly pest control logs
Sample transmittal to QC and Account Services
Review grounds logbook for Maintenance
Monthly audit of facility fire extinguishers
Other responsibilities as assigned by Senior Management