Planet Pharma
Base pay range
$35.00/hr - $50.00/hr 2-year contract Description: Individual contributor responsible for project providing support for a wide variety PCQT (Product Care and Quality Team) projects. Performs reagent-based or assay-based investigations to address reagent quality, performance or compliance on-market product issues. Scope includes primary stains, advanced staining reagents, special stains, and bulk reagents used for automated H&E, IHC (immunohistochemistry) and ISH (in-situ hybridization) applications. Works collaboratively across functions including Global Operations or Manufacturing, Complaint Investigation and Resolution, Global Customer Support, Lifecycles, Product Development, Quality, Regulatory, and Global organizations.
Responsibilities Designs a wide range of experimental protocols. Executes bench experiments; makes detailed and general observations and analyzes data. Prepares technical reports, summaries and quantitative analyses. Maintains complete and accurate records. Normally receives general directions on routine and new assignments. Identifies and implements improvements to work processes and laboratory environment. Works on complex problems in which analysis of situations or data requires an in-depth evaluation of various factors. Exercises judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results. Participates in cross functional technical teams such as a failure investigation or core team. Works well in a team environment by being a productive project team member, suggesting creative solutions to problems and providing input to project planning. Establishes interfaces across other organizational groups. Troubleshoots problems and institutes corrective action. Prepares and presents experimental procedures and results in group and project teams. Monitors work to ensure quality, and continuously promote Quality First Time.
Qualifications Formal Training/Education: Req: Bachelor's Degree Experience: Req: 4 years relevant job experience.
Seniority level Associate
Employment type Contract
Job function Research
Industries Pharmaceutical Manufacturing Biotechnology Research Medical Equipment Manufacturing
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$35.00/hr - $50.00/hr 2-year contract Description: Individual contributor responsible for project providing support for a wide variety PCQT (Product Care and Quality Team) projects. Performs reagent-based or assay-based investigations to address reagent quality, performance or compliance on-market product issues. Scope includes primary stains, advanced staining reagents, special stains, and bulk reagents used for automated H&E, IHC (immunohistochemistry) and ISH (in-situ hybridization) applications. Works collaboratively across functions including Global Operations or Manufacturing, Complaint Investigation and Resolution, Global Customer Support, Lifecycles, Product Development, Quality, Regulatory, and Global organizations.
Responsibilities Designs a wide range of experimental protocols. Executes bench experiments; makes detailed and general observations and analyzes data. Prepares technical reports, summaries and quantitative analyses. Maintains complete and accurate records. Normally receives general directions on routine and new assignments. Identifies and implements improvements to work processes and laboratory environment. Works on complex problems in which analysis of situations or data requires an in-depth evaluation of various factors. Exercises judgment within broadly defined practices and policies in selecting methods, techniques and evaluation criteria for obtaining results. Participates in cross functional technical teams such as a failure investigation or core team. Works well in a team environment by being a productive project team member, suggesting creative solutions to problems and providing input to project planning. Establishes interfaces across other organizational groups. Troubleshoots problems and institutes corrective action. Prepares and presents experimental procedures and results in group and project teams. Monitors work to ensure quality, and continuously promote Quality First Time.
Qualifications Formal Training/Education: Req: Bachelor's Degree Experience: Req: 4 years relevant job experience.
Seniority level Associate
Employment type Contract
Job function Research
Industries Pharmaceutical Manufacturing Biotechnology Research Medical Equipment Manufacturing
#J-18808-Ljbffr