Sterile Manufacturing Operator

Role: Manufacturing Engineer supporting pharmaceutical production, primarily in syringe packaging within a Penicillin facility. Responsibilities include providing technical support, preparing engineering documentation, conducting data analysis, executing tasks per SOPs, inspecting products, and maintaining GMP compliance. Requires collaboration with operations teams and adherence to safety standards. Qualifications: High School Diploma or GED with 2+ years in manufacturing, strong understanding of GMP, problem-solving skills, and ability to follow procedures. Preferred: experience in pharma manufacturing, proficiency with engineering software, knowledge of regulatory standards, and strong organizational skills. High-value biopharma specifics: involved in sterile injectable (syringe) manufacturing, cGMP compliance, and working in a union environment. Work setup: onsite with a 3pm-11:30pm shift, overtime, and potential extended hours; no travel mentioned.