Overview
Director, Pharmaceutical Quality Systems Jobs in Remote at Telix Pharmaceuticals (Americas)
JOB OVERVIEW
The Key Objective of the QC Inspector is to contribute to the growth and profitability of Multi-Pak by effectively executing the functions of Quality while providing additional support to the other senior managers. Specifically, under the general direction of the QC Manager, he/she is responsible and has commensurate authority for the following:
RESPONSIBILITIES:
Position Summary: The primary responsibility of this position is to inspect the production lines they are assigned for cleaning and packaging compliance. The person in this position is responsible for monitoring and enforcing compliance with the company’s SOPs and cGMPs.
Essential Functions:
Effectively monitoring and enforcing compliance with the company’s SOPs and cGMPs.
Overseeing and approving the clearing of production lines for the startup of production.
Overseeing that the requirements for Level I or Level II cleaning are met.
Execute validation activities as required by Protocols and Master Batch Records.
Perform Swab Testing on Packaging Equipment and Samples as per Multi-Pak, Client, Certification and Cleaning Validation requirements.
Verifying that the correct bulk and components were issued.
Confirm that packaging is completed according to specifications.
Responsible for completing quality checks
Completing paperwork per SOP and Client’s requirements.
Responsible for accepting or rejecting all in process or finished goods during inspections.
Ensuring that all quality and production documentation is properly completed and signed.
Investigating any production or inventory discrepancies when they arise.
Responsible for collecting and labeling Multi-Pak and Client samples as specified on the Master Packaging Specifications and Master Batch Record for each lot. Collected samples must be issued to the quality office or when required, shipped with the finished product.
Audits packaging lines to ensure all personnel are adhering to Multi-Pak procedures and policies; including but not limited to, following Personal Hygiene and PPE requirements, cGMP’s and Good Documentation Practices.
Nonessential Functions/Demands:
Training line operators on quality requirements and properly executing the requirements of the job.
Working on the production line, when required.
· Perform other related duties as assigned.
QUALIFICATION REQUIREMENTS:
A high school graduate with experience in quality in a packaging company.
Bi-lingual is a plus (English/Spanish).
Attention to detail a must.
REPORTING RELATIONSHIP:
Manager: QC Manager
Managerial Responsibility: None
PHYSICAL/MENTAL DEMANDS:
Must be able to lift-up to 20 pounds on occasion.
Must be able to remain in the stationary position for up to 30% of the time.
Must be able to walk or stand up to 100% of the time.
The person in this position is sometimes required to function in narrow aisles or passageways while walking throughout the production area.
The person in this position will need to occasionally kneel, climb, crawl, climb and/or reach to complete their job duties.
The person in this position is required to communicate to all other departments and must be able to exchange accurate information in these circumstances.
Job Type: Full-time
Pay: $23.00 – $24.00 per hour
Benefits:
401(k)
Dental insurance
Health insurance
Life insurance
Paid time off
Vision insurance
Schedule:
8 hour shift
Monday to Friday
Night shift
Work Location: In person
Title: Director, Pharmaceutical Quality Systems
Company: Telix Pharmaceuticals (Americas)
Location: Remote
