דרושים חברת פרמייר

Requirements:
Bachelors degree in Biomedical Engineering, Mechanical Engineering, Quality Assurance, or related field.
Minimum of 3 years of experience in a Quality Assurance role within a medical device manufacturing environment.
Strong knowledge of FDA regulations (21 CFR 820), ISO 13485, and other relevant standards.
Familiarity with clean room protocols and sterilization methods for medical devices (e.g., EO sterilization, steam sterilization).
Strong analytical and problem-solving skills, with the ability to assess complex production issues.
Excellent communication skills, both verbal and written, with the ability to effectively collaborate across teams.
Detail-oriented and highly organized, with the ability to manage multiple priorities in a fast-paced environment.
Proficient in Microsoft Office Suite (Excel, Word, PowerPoint).