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Resumes 81 - 90 of 304 |
Trenton, NJ
... in process logs and machine down time ●Ensure all drums are properly labeled ●Ensure work area is clean and maintained in a c GMP environment ●Ensure equipment usage and room logs are properly maintained ●Must remain at machine at all times during ...
- 2020 Oct 07
Hillsborough Township, NJ
... ●Contributes expertise and provides guidance in 21 CFR Part 11, GAMP5, and EU GMP Annex 11 requirements and data integrity principles and requirements as well as participates in assessments. ●Develops and evaluates quality processes and system ...
- 2020 Oct 06
Monmouth Junction, NJ
... • Training of the new employees or re-training of the old employees for Basic GMP Series. • Planning for samples sending to outside laboratory which are not possible to analyze in the department and checking of its records. • Monitor monthly indent ...
- 2020 Sep 30
Ringoes, NJ
... Trained in SOP/SQF/GMP/HACCP, lockout/tagout, and maintained production lines and performed PM’s Dec. 03 To July 09 International Technidyne Corp., Edison, NJ. Production Mechanic Respond to, identify, and correct production equipment problems / ...
- 2020 Jun 26
Milltown, NJ
... Proven ability to work efficiently and effectively in a fast paced GMP/GLP environment. Demonstrated success in using knowledge and experience to interpret and properly enter testing data into LIMS. EDUCATION BS, Bachelor Degree of Science, ...
- 2020 Jun 07
Bristol, PA
... Provided manufacturing process development and validation support, identified in-control and out-of-control processes, formulated quality and production improvement plans, and assisted with GMP and cGMP activities. Managed laboratory maintenance and ...
- 2020 Apr 27
Somerset, NJ
... Experience in working with Search skills like,GMP,CGMP,GLP,validation,Technical writing, Sop writing, GMP Documentation,Manufacturing,Data Analysis,bench scientist, SQL, Oracle, Cell Culture,Elisa,Molecular Filed etc…… UDP International Human ...
- 2020 Mar 08
East Brunswick, NJ
... Proven expertise in: •Strategic Project Management •Product Development & Management •Inventory Control •Root Cause Analysis •Lean Six Sigma, Kaizen Events, & 5S •FDA/GMP/OSHA Requirements •Cost & Risk Mitigation •Value Stream Mapping •Continuous ...
- 2020 Feb 28
Hightstown, NJ
... Batch paperwork Perform final documented review of completed batch paperwork prior to shipment and final review of all other GMP documents Documentation responsibilities include the initiation of SOP changes, processing new and revised SOPs, ...
- 2020 Feb 21
Trenton, NJ
... Successfully executed packaging line implementations and commissioning as engineering lead from concept to commercialization with GMP and FDA requirements. Highly organized and efficient with proven technical skills and ability to motivate. ...
- 2020 Jan 14