Clinical Quality Assurance Career Research and Resources
ISP Pharma Technologies
Reviews all R@D and GMP batch records. Performs in-process QA checks during granulation, tableting an encapsulation. Engages in shipment of products
Avg. Salary: $48,000 · Company Rank: Not Available
Baxter BioSciences
Performs review of QC test records (water and process air). Assist in review of manufacturing batch records. Provide support and guidance to material handlers during shipment.
Avg. Salary: $48,000 · Company Rank: Not Available
Irvine Pharmaceutical Services
• Qualified to perform Internal Company Quality Audits • Responsible for the implementation of an in-process review system and SOP to minimize errors in the laboratory in accordance to cGMP, USP and ICH guidelines. • Work with QA for review, investigation and approval of scientific projects. • Manage different schedules simultaneously and meet project deadlines by working closely with Project Management. • Lab Approve...
Avg. Salary: $55,000 · Company Rank: Not Available
Ulitmate Marketing Concepts
• Managed and Coordinated all Conferences, Seminars and Vendor Shows • Provided project plans and timelines to the project management team • Reviewed Client Marketing Material prior to printing • Assisted in the layout of new marketing material • Able to Lead, Supervise and Coordinate groups by providing necessary information and dedication to all projects in a team environment and independently with 100% dedication.
Avg. Salary: $55,000 · Company Rank: Not Available
Quest Diagnostics-Nichols Institute
• Lead and trained all new critical reagents group members in the conjugation, biotinylation, data reduction and process for the immunodiagnostic group. • Responsible for protein Conjugation of critical reagents used for all chemiluminescent NID assays, both automated and manual. Conjugation was both with biotin and acridinium and included product purification, qualification, release, R&D and troubleshooting of all immuno...
Avg. Salary: $55,000 · Company Rank: Not Available
Bachem California
QC Chemist • Test and release raw material to meet GMP compliance through wet chemistry techniques • Prepared buffers, reagents and solvents for instrument use • Maintained and calibrated analytical equipment • Sampled and analyzed water quality and reviewed results • Identified and researched microbiological organisms for environmental quality • Basic training in Beckman HPLC and GC
Avg. Salary: $55,000 · Company Rank: Not Available
MAP Pharmaceutical
Manages characterization, formulation and aerosol laboratories. Ensures equipment functioning, maintenance and calibration scheduling. Schedules instrumentation usage time according to projects priorities. Analytical data release. Laboratory supplies purchasing. Capital equipment purchasing sourcing, management and coordination. Equipment installation. Coordinates with different vendors on methods/technology transfer, ...
Avg. Salary: $110,000 · Company Rank: Not Available
Neosil Inc.
Planned, organized and established a new startup GLP analytical laboratory. Purchased and installed all instrumentation. Wrote all laboratory SOP’s, methods, protocols, calibration, PQ and PM procedures. Provided instrument (UV-Vis, FTIR, HPLC-GPC, RP, NP, Chiral) and analytical software training for all group members. Maintenance and troubleshooting of all laboratory instruments. Conducted stability, degradation studies, ...
Avg. Salary: $110,000 · Company Rank: Not Available
Stabford Research International
Train/mentor scientists on instrument (UV-Vis, FTIR, GC, HPLC, LC-MS) and analytical software use and maintenance. Wrote training materials for instrument use, maintenance and applications. Developed and transferred methods including client training and support for GPC-Agilent Molecular Weight Determination software. Developed material specifications, test methods, validation and stability protocols according to FDA and ICH...
Avg. Salary: $110,000 · Company Rank: Not Available
Alza Corp.
Instrument (HPLC) and analytical software application training, troubleshooting and maintenance for new employees. Wrote protocols, reports and SOP’s. Developed and validated methods and data for IND level submissions. Planned and conducted stability and degradation studies, RS qualification, drug release rate testing, technical reports and data review. Generated analytical stability data necessary for IND and NDA submiss...
Avg. Salary: $110,000 · Company Rank: Not Available
