Company:
Tucker Parker Smith Group (TPS Group)
Location: Irvine
Closing Date: 19/11/2024
Hours: Full Time
Type: Permanent
Job Requirements / Description
Quality System Specialist
12-month position (potential to extend)
Irvine, CA
Pay: $32-$36/HR
Our client, a leading life science and research company is looking for a Quality System Specialist to join their team. This position will support the compilation and maintenance of IVDR technical files, review IVDR and other registration labeling change requests and various quality tasks to support the QMS overall.
How You'll Make An Impact:
Review, approve, and process labeling and FOC change requests
Compile, create, review, and update quality related technical file documentations (i.e. DMR updates, compile finished product testing documents, etc)
Various quality tasks such as LS FOC creation, non-labeling related change requests, etc
What You Bring:
Education: Bachelors degree preferred or high school diploma/equivalent with 2 to 3+ years of work experience
Work Experience: 2+ years experience in Quality, Documentation Control, Change Control process, GMP
Basic understanding of GMP and quality system standards
Proficient in Microsoft office (word, excel, etc)
Please submit your resume in Word or PDF format to be considered.
Quality System Specialist
12-month position (potential to extend)
Irvine, CA
Pay: $32-$36/HR
Our client, a leading life science and research company is looking for a Quality System Specialist to join their team. This position will support the compilation and maintenance of IVDR technical files, review IVDR and other registration labeling change requests and various quality tasks to support the QMS overall.
How You'll Make An Impact:
Review, approve, and process labeling and FOC change requests
Compile, create, review, and update quality related technical file documentations (i.e. DMR updates, compile finished product testing documents, etc)
Various quality tasks such as LS FOC creation, non-labeling related change requests, etc
What You Bring:
Education: Bachelors degree preferred or high school diploma/equivalent with 2 to 3+ years of work experience
Work Experience: 2+ years experience in Quality, Documentation Control, Change Control process, GMP
Basic understanding of GMP and quality system standards
Proficient in Microsoft office (word, excel, etc)
Please submit your resume in Word or PDF format to be considered.
Share this job