(MENLO PARK, CA)
There is no greater calling or opportunity for a fluid management company than today’s challenge – helping customers protect people, the environment and our natural resources.
Together we are implementing technologies that purify and conserve water, consume less energy, make alternative energy sources possible and practical, advance medicine and minimize emissions and waste.
Our collective efforts are enabling a greener more sustainable future.
Pall is a Fortune 1000 materials science and engineering company with the broadest filtration, separation and purification capabilities in the world. Our process and product enabling technologies help our customers make good products better, safer and even possible. We provide innovative products to customers in health care, biotechnology, pharmaceutical, semiconductor, municipal drinking water, aerospace, food and beverage and industrial manufacturing markets. Headquartered in Long Island, NY, Pall has operations in every major country.
QC ASSOCIATE – MENLO PARK, CA
The QC Associate performs Quality Control Testing of Octet and MicroReactor24 Instruments. The QC Associate will also be involved in the Testing and Validation of calibration tools for the Genedisc cycler.
The QC Associate performs an initial evaluation of product performance, analyzes Quality Control data and reports test results and observations to QC Manager for product release. The QC Associate needs to develop a very detailed understanding of the instrumentation and consumables in testing and the applied QC tests. The QC Associate performs the product testing independently without supervision and does an initial evaluation of the product performance. This person will summarize, track and communicate testing results.
Quality Control Testing of Octet and MicroReactor Instruments.
Testing and Validation of Calibration Tools for Genedisc Cycler.
Data analysis to report test results.
Maintenance of existing Quality Control protocols and documentation.
Cross train on QC procedures for other PALL products manufactured in Menlo Park.
Analyze experimental data and prepare documentation required for product release to Finished Goods Inventory.
Clearly communicate and document test results.
Maintain QC documentation and databases for performance tracking.
Maintain inventory of materials needed for QC Testing.
Participate in other QC activities as needed.
BS in Life Sciences and a minimum of 6 months laboratory experience.
Demonstrated experience with PCR techniques, SOP’s, Laboratory Instruments and documentation/reporting.
Proven experience working as part of a collaborative team and cross functional team working is essential.
Experience with Excel and data management preferred.
Experience in cGMP and/or cGLP a plus.
To apply for this position please visit our career site at www.pall.com .
The tracking code for this position is LW-120823115426
Equal Opportunity Employer
M / F / D / V
Pall Corporation is committed to equal opportunities to all without regard to race, color, religion, sex, sexual orientation, national origin, citizenship, age, marital status, disability, veteran's status or any other personal trait protected by federal, state or local law.
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