Qa Floor Inspector 3Rd Shift Jobs

Minimum Required Skills And Knowledge

Experience with HCM (e.g., Workday) or equivalent ERP product and productivity software desired.

Excellent written and verbal communication skills

Performs inspections, checks testing and sampling procedures for product manufacturing processes.

Monitors critical equipment and instrumentation.

May draft procedures and assist with validating or troubleshooting testing methods, including assays.

Adhere to all Zenith Management Company standards

Ability to communicate satisfactorily with guests, management, and co-workers.

Reports to Building Manager or Housekeeping Executive any unexpected vacant rooms

Have knowledge of fire alarm/carbon monoxide alarm and evacuation procedures

Responsible to inspect for cleanliness of guest rooms, public areas and for reporting any

Inspect bed and bathroom linens for cleanliness and condition. Pull any item not up to

Perform live review of manufacturing batch records in preparation for batch release and escalate any discrepancies immediately.

Assist functional areas with achieving timely and compliant final product disposition of the product.

Review, approve and support procedures and production/testing records as required and assist in the training of site associates.

Ensure compliance of site personnel and application of aseptic techniques and full compliance to sterile manufacturing regulations.

Support FDA/Regulatory interactions for the site activities and products to ensure successful regulatory submissions and inspections.

Other related duties as assigned.

Assemble quality data to support management review meeting requirements

Identify and report any non-conformances and/or discrepancies to management if applicable.

Complete other duties or participate in project work as assigned by management.

Advanced training or education in pharmaceutical quality compliance or related field of study from an accredited college/university.is preferred.

Minimum of three (3) years’ experience in a quality assurance in a GMP pharmaceutical work environment.

Effective interpersonal relationship skills and the ability to work in a team environment.

High school diploma or general education degree (GED), required required.

QA experience in manufacturing, required

Have strong organizational skills and attention to detail

Schedule: Sunday night-Friday morning with opportunities for overtime

Performs in-process testing verifications, submits samples for testing, and conducts AQL as required

Approves pre-start-up activities and checks equipment for proper functioning