Thousand Oaks, CA USA
This is Kacy, from CompNova.
We have a NEW job position and would like to share with you, if you are looking for a job/change please let me know your thoughts by replying to this email email@example.com you can reach me at 469-329-1500 Ext.503
If you are not available or not suitable for this role please accept my apologies. I appreciate & will be thankful for your support with few references from your network that are looking for a job.
Position: Associate QA
Location: Rhode Island
JOB ID: AMAGJP00002432
Top 3 skills:
Attention to detail
Proficient in Microsoft Office Systems and previous experience in GMP Quality Systems (i.e. LIMS)
Support the Corporate Product Quality department through the entry, verification, review, tracking, and archiving of technical data. Required skills include knowledge of GMP, 2-3 years operational experience in pharmaceutical or regulated industry; data entry; data verification; clerical and/or administrative experience; proficient in MS Excel, Word, PowerPoint, MS Project.
The successful candidate will:
Perform transcriptional data verification of technical reports and other documents, following corporate Standard Operating Procedures.
Enter documents into corporate quality GMP Lab databases, checking for completion and correctness.
Enter data from external sources into MS Excel spreadsheets or MS Word documents.
Gather documents and materials, collates, distributes and/or files.
Enter and distribute documents and forms.
Data processing support to include maintaining database for all documentation.
Audit reports and files for discrepancies.
May compile information and metrics from various documents or databases.
Provide guidance or refer staff members to appropriate contacts.
Coordinate or manage multiple documents and team members t
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||Biotech / Pharma
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