Manufacturing Tech I
Minnetonka, MN (onsite)
Schedule:
2nd Shift (Monday to Thursday, 4:20pm - 2:50am)
Duration:
8-Month Contract
Pay:$20-25/ph
Training Schedule:
Monday to Thursday, 6:00am - 4:30pm, 1-2 weeks of training depending on their ability to complete their training tasks.
We are seeking a Manufacturing Technician
I
to join our biotech client’s pharmaceutical production team. This role is responsible for supporting both routine and complex tasks related to the Good Manufacturing Practice (GMP) compliant assembly and packaging of combination pharmaceutical products. The technician will play a critical role in documentation, production activities, inspection, and final packaging processes. The ideal candidate is detail-oriented, team-driven, and committed to quality and safety.
Job Responsibilities:
In this role, you will perform hands-on work in a GMP-regulated environment, contributing to the manufacturing and packaging of pharmaceutical products. Key responsibilities include:
- Executing assembly, final packaging, and inspection of pharmaceutical products per standard operating procedures (SOPs) and work instructions (WIs).
- Adhering to manufacturing and quality standards, including proper documentation practices and traceability.
- Receiving and distributing materials within the production area.
- Meeting defined production metrics while maintaining compliance with all quality and safety standards.
- Participating in ongoing training and continuous improvement initiatives.
- Performing other related duties as assigned.
Essential Duties and Job Functions:
- Follow cGMP and company guidelines for production and documentation.
- Operate in controlled or clean room environments with proper gowning protocols.
- Maintain compliance with documentation standards such as Good Documentation Practices (GDP).
- Accurately complete batch records and associated production documentation.
- Collaborate with team members and other departments to meet daily production goals.
- Safely operate manufacturing equipment and troubleshoot as necessary.
Knowledge & Skills:
- Familiarity with executing SOPs in a manufacturing or regulated environment.
- Understanding of quality systems including cGMP and GDP.
- Strong attention to detail and accuracy in documentation.
- Ability to lift up to 50 pounds and perform physically demanding tasks (e.g., standing for long periods, manual assembly).
- Excellent communication and organizational skills.
- Ability to work independently and collaboratively within a fast-paced team environment.
Education & Experience:
- High school diploma or equivalent required.
- Previous experience in a manufacturing setting preferred; experience in pharmaceutical or biotechnology environments is a plus.
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