Hydrogen Group
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).
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).