Quality Manager V

PSG Global Solutions; Swiftwater; On-site; CAD 30,000 - 60,000; Full time

Job summary

An innovative firm is seeking a Quality Manager V to oversee critical validation activities in the Pharmaceuticals and Medical Products industry. This role involves participating in project teams for biotech facilities and ensuring compliance through the review and approval of validation studies. The successful candidate will play a pivotal role in maintaining the highest quality standards for drug substance and product vaccines. Join a forward-thinking organization that values excellence and offers the opportunity to make a significant impact in a vital industry.

Responsibilities

• Participate in project teams for biotech facilities and processes.
• Review and approve validation studies for assigned areas.
• Signatory responsibilities for validation documents.

Job description

Description

We're looking for a Quality Manager V, working in Pharmaceuticals and Medical Products industry in Discovery Drive, Swiftwater, Pennsylvania, 18370, United States.

Key Accountabilities:

• Participate in project teams involved in site biotech facilities, processes and equipment for the manufacture of Drug Substance and/or Drug Product Vaccines.
• Review and approve validation related studies for assigned areas. These assigned areas would include validation lifecycle activities such as Validation Planning, Biotech Process.
• Validation, Equipment and Facility Qualification and Validation Risk Management.
• Signatory responsibilities for validation/qualification documents within assigned areas.