Technician 2, Manufacturing (2nd Shift)

Antares Pharma • Minnetonka, MN

4d • Onsite

About The Position

The Technician 2, Manufacturing will be responsible for performing routine and complex tasks for the GMP manufacturing and packaging of pharmaceutical products at the Minnesota Operations Facility. The Technician 2, Manufacturing will be familiar with best practices for cGMP assembly and packaging of combination pharmaceutical products. This individual is responsible for the documentation and the hands-on execution of production activities related to assembly, final packaging, and inspection of manufactured pharmaceutical products. In this role, you’ll have the opportunity to:
Responsible for quality and adheres to all manufacturing process and quality requirements according to Halozyme quality processes
Receives and distributes supplies in the manufacturing area
Operates and monitors manufacturing equipment to produce clinical and commercial pharmaceutical products under minimal supervision
Performs the assembly, final packaging, and inspection of pharmaceutical products
Assembles products following all current Standard Operating Procedures (SOPS) and Work Instructions (WIs), while meeting manufacturing goals and metrics
Ability to maintain accurate records following Good Documentation Practices (GDP) and current Good Manufacturing Practices (cGMP) guidelines including training files and shop floor paperwork
Provides feedback to management on recommendations for procedural and process improvements
Other duties as assigned

Requirements

• Minimum High School Diploma with 1-3 years of work experience in a manufacturing environment
• An equivalent combination of experience and education may be considered
• Must be able to work in a controlled or clean room environment requiring special gowning
• Critical understanding of the importance of documentation and data traceability
• Experience utilizing automated and/or laboratory equipment
• Must have the ability to work safely and responsibly in a manufacturing environment
• Basic understanding of LEAN Manufacturing methodologies
• Comfortable utilizing computers in the workplace and familiar with Microsoft 356
• Ability to multi-task and adjust priorities, as necessary
• Excellent organizational skills
• Demonstrated attention to detail
• Familiarity with executing Standard Operating Procedures (SOPs) in a manufacturing or assembling environment, preferably in the pharmaceutical industry
• Must be able to work well independently and in a team environment
• Demonstrated ability to perform product and/or process investigations preferred
• Excellent communication skills, both verbal and written

Responsibilities

• Responsible for quality and adheres to all manufacturing process and quality requirements according to Halozyme quality processes
• Receives and distributes supplies in the manufacturing area
• Operates and monitors manufacturing equipment to produce clinical and commercial pharmaceutical products under minimal supervision
• Performs the assembly, final packaging, and inspection of pharmaceutical products
• Assembles products following all current Standard Operating Procedures (SOPS) and Work Instructions (WIs), while meeting manufacturing goals and metrics
• Ability to maintain accurate records following Good Documentation Practices (GDP) and current Good Manufacturing Practices (cGMP) guidelines including training files and shop floor paperwork
• Provides feedback to management on recommendations for procedural and process improvements
• Other duties as assigned

Benefits

• Employee Stock Purchase Program
• 401(k) matching
• Opportunities to grow in a culture that prioritizes learning, development and progression through in-house programs
• Tuition reimbursement

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Education Level: High school or GED