PSG Global Solutions
Quality Control Analyst
PSG Global Solutions, Summit, New Jersey, us, 07902
At Real we're always looking for new and ambitious people to help deliver exceptional service levels, change the lives of the candidates we represent and partner with some of the world's best pharmaceutical, biotechnology and medical companies.As specialists in recognising talent we pride ourselves on not just finding the best people for our client partners but on our ability to spot the best and brightest talent to work for us. We are also renowned for providing training and long-term career opportunities to help our employees be the best they can be, so they can continue to deliver the expertise Real has become famous for.Relationships are at the heart of everything we do and ensure that our clients and candidates continue to work with us again and again. This ethos is also what shapes how we work as a business. We encourage and reward knowledge sharing and have various support networks and international forums to enable our employees to keep up-to-date with changes happening across their industries and share local insight to deliver true global perspectives.Job Description
Responsible for assisting with laboratory analysis for clinical release and routine stability testing. May conduct routine release and stability analyses of developmental compounds, prototype formulations and finished products in support of clinical testing for IND and NDA submissions.Perform laboratory analysis under guidance of a supervisor or designee.Responsibilities will include, but are not limited to, the following:Able to conduct testing independently and may assist other analysts in analytical testing including HPLC, dissolution, Karl Fischer, UV/Vis and other analytical laboratory testing.Conducts routine analytical experiments using analytical methods and procedures.Draws basic conclusions from data and results and communicates with other analysts and management.Performs instrument/method troubleshooting within analytical method parameters and management guidance.Performs testing for development and commercial samples, release and stability samples in accordance with established methods, specifications and protocols with limited supervision.Good laboratory documentation skills.Documents/reviews laboratory work using laboratory notebooks/worksheets that is detailed, timely and in compliance with GLP/cGMP requirements.Other duties as assigned by management.Qualifications
BS/MS Chemistry or relevant discipline with equivalent experience.Minimum 2 - 4 years recent cGMP/GLP pharmaceutical laboratory experience.Experience with HPLC, dissolution, FT-IR, UV/Vis spectrophotometry, KF.Able to work well in team environment to achieve results.Exhibits sound scientific judgment based on reasonable assumptions and available information.
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Responsible for assisting with laboratory analysis for clinical release and routine stability testing. May conduct routine release and stability analyses of developmental compounds, prototype formulations and finished products in support of clinical testing for IND and NDA submissions.Perform laboratory analysis under guidance of a supervisor or designee.Responsibilities will include, but are not limited to, the following:Able to conduct testing independently and may assist other analysts in analytical testing including HPLC, dissolution, Karl Fischer, UV/Vis and other analytical laboratory testing.Conducts routine analytical experiments using analytical methods and procedures.Draws basic conclusions from data and results and communicates with other analysts and management.Performs instrument/method troubleshooting within analytical method parameters and management guidance.Performs testing for development and commercial samples, release and stability samples in accordance with established methods, specifications and protocols with limited supervision.Good laboratory documentation skills.Documents/reviews laboratory work using laboratory notebooks/worksheets that is detailed, timely and in compliance with GLP/cGMP requirements.Other duties as assigned by management.Qualifications
BS/MS Chemistry or relevant discipline with equivalent experience.Minimum 2 - 4 years recent cGMP/GLP pharmaceutical laboratory experience.Experience with HPLC, dissolution, FT-IR, UV/Vis spectrophotometry, KF.Able to work well in team environment to achieve results.Exhibits sound scientific judgment based on reasonable assumptions and available information.
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