Overview
GMP Manufacturing Process Operator Jobs in Whitchurch-Stouffville, Canada at Teva Pharmaceuticals
Title: GMP Manufacturing Process Operator
Company: Teva Pharmaceuticals
Location: Whitchurch-Stouffville, Canada
Category:
Location: Whitchurch-Stouffville
Drive excellence as a GMP Manufacturing Process Operator. Contribute to pharmaceutical production with a focus on safety, quality, and operational efficiency in a night shift setting.
In this role, you will manufacture crucial products by following precise protocols and regulatory standards. Your primary responsibilities include managing equipment for multiple processes and documenting all activities with accuracy. Work collaboratively to maintain high quality and safety throughout the production process.
Key Responsibilities:
• Operate production equipment per Master Batch Record
• Ensure compliance through detailed GMP documentation
• Manage multiple processes and perform checks
• Engage in ERP data entry and verification
• Facilitate cleanliness and maintenance within GMP areas
Requirements:
• 1+ year of experience in a GMP environment
• High School diploma or equivalent required
• Strong mechanical skills for machinery
• Proficient in Windows applications and SAP
• Ability to multitask and problem-solve independently
Become a part of a team committed to quality and health improvement through innovative manufacturing practices.
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