Hello,
This is Das from IntellecttINC we are working with Medical Device Manufacturing clients.
At this moment we are looking for candidates for the
Quality Control Technician position who can do these below mentioned job duties, Please go through it and let me know if you are interested or if not try to help who would be interested by sharing.
Interested please share your resume to das@intellectt.com or can reach me on phone +1 732-201-5142 (WhatsApp for quicker response (wa.me/+17322015142))
Role: Quality Control Technician
Location: Scarborough, ME
Start Time (AM/PM):
2:30pm-11pm, either Sun-Thurs or Tues-Sat
Job Description
- Perform a wide variety of activities to support the Quality Management System.
Essential Duties And Responsibilities
- Conduct product testing, including testing to support complaint investigations and stability verification
- Generate product testing results reports
- Review production batch records (DHR's) for accuracy and completeness in order to approve intermediate products for use in production.
- Review finished goods batch records.
- Report all deviations in these records and assure these have been addressed and resolved prior to issuing approval.
- Conduct spot-check inspections/audits of production operations
- Participate in the internal audit program
- Write, review and approve Standard Operating Procedures (SOPs) as necessary
- May assist in supporting the Document Control program, record retention areas, and sample retention areas
- May support returned instrument processing
- Log returned instruments from the field.
- Decontaminate returned instruments in a Biohazard level II environment following standard operating procedure and documenting decontamination as required.
- Inspect returned instruments for damage, and performed basic investigation and documenting results prior to second level processing.
- As necessary, process instrument documentation for return to the repair facility, and pack instruments as required.
- Other duties as assigned by supervisor
Qualifications
- To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.
- The requirements listed below are representative of the knowledge, skill, and/or ability required.
- Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions.
- Ability to follow Good Manufacturing/Laboratory Practices (GMP and GLP)
Education And/or Experience
- Bachelor's degree in a scientific or technical area or equivalent combination of experience and education.
- At least one year in a quality assurance role in the medical device industry is preferred.
If anyone interested please share your resume to das@intellectt.com or can reach me over the phone.
Direct: +1 732-201-5142 (WhatsApp for quicker response (wa.me/+17322015142))