Manufacturing Technician I
Minnetonka, Minnesota
Schedule:
6:00am to 4:30pm (Monday through Thursday)
Duration:
3-month contract
Pay:$20-24/ph
Job Summary:
The Manufacturing Technician I is responsible for executing both routine and complex tasks related to the GMP manufacturing and packaging of pharmaceutical products. This role involves hands-on assembly, final packaging, and inspection activities while adhering to current Good Manufacturing Practices (cGMP). The ideal candidate will be well-versed in cGMP standards for combination pharmaceutical products and demonstrate a strong commitment to quality, safety, and operational excellence.
Job Responsibilities:
In this role, you will support the production of pharmaceutical products in a controlled environment. Key responsibilities include:
- Performing assembly, packaging, and inspection tasks in accordance with current Standard Operating Procedures (SOPs) and Work Instructions (WIs).
- Following manufacturing protocols and quality requirements under cGMP and Good Documentation Practices (GDP).
- Receiving and managing inventory of manufacturing supplies.
- Completing production documentation accurately and on time.
- Collaborating with team members to meet manufacturing goals and quality standards.
- Participating in training and maintaining up-to-date training records.
- Supporting continuous improvement efforts and performing other duties as assigned.
Essential Duties and Job Functions:
- Execute assembly and packaging tasks per SOPs, maintaining compliance with internal quality standards.
- Document all production activities with precision to ensure traceability and compliance.
- Perform visual inspections of final products for quality assurance.
- Follow gowning procedures and operate within controlled/cleanroom environments.
- Engage in physical activity including lifting (up to 50 lbs), standing, and manual tasks as needed.
- Contribute to a safe, clean, and organized work environment in accordance with safety and GMP regulations.
Knowledge & Skills:
- Familiarity with cGMP guidelines and GDP.
- Strong attention to detail and commitment to documentation accuracy.
- Ability to work both independently and collaboratively in a team setting.
- Effective verbal and written communication skills.
- Organizational skills to manage time and tasks effectively.
- Comfortable working in cleanroom environments requiring specific gowning protocols.
- Understanding of basic manufacturing principles; pharmaceutical experience is a plus.
Education & Experience:
- High School Diploma or equivalent required.
- Prior experience in a regulated manufacturing environment preferred (pharmaceutical or biotechnology industry is a plus).
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