Date Posted: 11/06/2024

*Hiring Organization: *Rose International

*Position Number: *473922

*Job Title: *Production Worker - 1st Shift

*Job Location: *Sturgis, MI, USA, 49091

*Work Model: *Onsite

*Shift: *07:30am - 4:00pm EST

*Employment Type: *Temporary

*Estimated Duration (In months): *5

*Min Hourly Rate($): *18.50

*Max Hourly Rate($): *18.50

*Must Have Skills/Attributes: *Manufacturing

*Nice To Have Skills/Attributes: *Assembler, Assembly

Required Education: High School Diploma or Equivalent Preferred Education: NA

Required license/Certification: NA Preferred License/Certification: NA

Required Qualifications/Skills/Experience: • Previous experience in product inspection, packaging, or a similar role preferred. • Familiarity with Good Manufacturing Practices (GMP) and quality control standards. • Detail-oriented mindset with strong observational skills. • Ability to follow protocols and maintain clean-room standards as needed. • Basic record-keeping skills for accurate documentation. • Moderate supervision is required, so the ability to work independently with minimal oversight is important.

Preferred Qualifications/Skills/Experience: • NA

Job Overview: We are seeking a detail-oriented and motivated Product Inspector and Packaging Specialist to join our team. In this role, you will play a critical part in our production process, ensuring that both raw materials and finished products meet our high standards of quality.

You will be responsible for inspecting, labeling, and packaging products accurately and maintaining records in compliance with Good Manufacturing Practices (GMP). This role may also involve working in a clean-room environment to maintain product integrity.

Job Duties: • Inspect and Ensure Quality: Examine raw materials and finished products to confirm they meet our quality and safety standards. • Accurate Labeling and Packaging: Label and package products with precision, ensuring compliance with product specifications and labeling requirements. • Maintain GMP Records: Accurately document inspection findings and packaging records according to GMP standards to support compliance and traceability. • Work in a Clean-room Environment: Follow specific protocols to maintain a sterile work environment when required to ensure the highest standards of cleanliness and quality. • Collaborate with Team: Work closely with the production team and quality control personnel to resolve any quality issues that may arise.

Industry: Medical Device or Manufacturing Estimated Start Date: 12/16/2024 Location: Sturgis MI Trav