Senior Technician 1, Quality Control

Antares Pharma Inc.; Hopkins (MN); On-site; Full time

Job summary

A leading company in pharmaceutical manufacturing is looking for a Senior Technician 1, Quality Control for their Minnetonka office. This full-time position supports the quality control function through inspection, testing, and teamwork while ensuring compliance with ISO and GMP standards, contributing to patient safety and product efficacy.

Qualifications

• At least 2 years of experience in a quality control role within ISO and GMP systems.
• Ability to collaborate with technical, R&D, manufacturing, and regulatory teams.

Responsibilities

• Perform lot release testing and data recording.
• Conduct inspections and provide peer review.
• Lead training exercises and support manufacturing.

Skills

Collaboration

Statistical analysis

Quality assurance principles

Education

High School diploma

Tools

Microsoft Excel

Job description

Join to apply for the Senior Technician 1, Quality Control role at Antares Pharma Inc.

Position Overview

We are seeking a Senior Technician 1, Quality Control for the second shift at our Minnetonka, MN office. Join us to be part of a culture that values diversity, innovation, and collaboration, and make a meaningful impact on patients' lives.

Responsibilities

1. Perform lot release testing, data recording, and basic statistical analysis.
2. Conduct receiving inspections on incoming materials, including visual examinations and measurements.
3. Provide independent peer review of work done by other technicians.
4. Assemble samples for testing and document inspection results.
5. Monitor incoming product quality and report observations.
6. Maintain measurement equipment and monitor calibration status.
7. Identify and report NCRs/Deviations.
8. Participate in Quality System improvements via CAPA processes.
9. Lead training exercises and support manufacturing activities.
10. Provide mentorship and training to team members.

Qualifications

• High School diploma with at least 2 years of experience in a quality control role within ISO and GMP systems.
• Ability to collaborate with technical, R&D, manufacturing, and regulatory teams.
• Proficiency with Microsoft Excel or similar software.
• Knowledge of GxP, 21CFR, ISO, QSR, and related regulations.
• Strong technical background and quality assurance/control principles.

Additional Information

This is a full-time onsite position, working 4 days of 10 hours each. The typical pay range is $23.00 - $32.00 per hour, with shift differentials. Total compensation may include bonuses and equity awards.

We are committed to providing reasonable accommodations for qualified individuals with disabilities. Contact Human Resources at [e-mail] for assistance.

Employment Details

• Seniority level: Mid-Senior level
• Employment type: Full-time
• Job function: Quality Assurance
• Industry: Pharmaceutical Manufacturing