Indotronix Avani Group
Essential Functions
Assemble and test medical device assemblies, final products, and accessories per the manufacturing documentation provided. Perform assembly diagnosis, repair, and test equipment maintenance with supervision. Ensure work is completed in compliance with the company quality system and medical device regulations. Assemble, test, and repair work per established work instructions, policies and procedures. Performs assembly diagnosis and repair. Notify the area supervisor and/or team lead of quality concerns. Operating within standard operating procedures (SOPs) and assembly drawings. Provide guidance in problem diagnosis and resolution with team members. Assist in the development and revisions of Standard Operating Procedures (SOP), Work Instructions (WI), and Device History Records, or other quality documentation, as necessary, to support production processes. Education / Experience / Skills
Bachelor’s degree in engineering or a related scientific field. Associate’s degree with 2+ years’ experience or High School Diploma with 6+ years of experience in a similar position. Desired Qualifications
Experience working in a cGMP setting and controlled documentation, SAP, and Six Sigma belt, or LEAN ideology. Seniority level
Associate Employment type
Contract Industries
Medical Equipment Manufacturing, Pharmaceutical Manufacturing, and Biotechnology Research
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Assemble and test medical device assemblies, final products, and accessories per the manufacturing documentation provided. Perform assembly diagnosis, repair, and test equipment maintenance with supervision. Ensure work is completed in compliance with the company quality system and medical device regulations. Assemble, test, and repair work per established work instructions, policies and procedures. Performs assembly diagnosis and repair. Notify the area supervisor and/or team lead of quality concerns. Operating within standard operating procedures (SOPs) and assembly drawings. Provide guidance in problem diagnosis and resolution with team members. Assist in the development and revisions of Standard Operating Procedures (SOP), Work Instructions (WI), and Device History Records, or other quality documentation, as necessary, to support production processes. Education / Experience / Skills
Bachelor’s degree in engineering or a related scientific field. Associate’s degree with 2+ years’ experience or High School Diploma with 6+ years of experience in a similar position. Desired Qualifications
Experience working in a cGMP setting and controlled documentation, SAP, and Six Sigma belt, or LEAN ideology. Seniority level
Associate Employment type
Contract Industries
Medical Equipment Manufacturing, Pharmaceutical Manufacturing, and Biotechnology Research
#J-18808-Ljbffr