QC Analyst- Material Qualifications

Regeneron Pharmaceuticals

4d • $24 - $38 • Onsite

About The Position

Regeneron is currently looking for a Quality Control (QC) Analyst on our Materials team with a 1st shift, Monday-Friday, 8am-4:30pm schedule. Regeneron successfully manufactures a range of biopharmaceuticals for patients worldwide, including our approved therapeutic proteins and those involved in clinical studies. Our QC Analysts are responsible for the operations of the QC Reference Standard and QC Materials functional area activities. They openly communicate with Regeneron QC Laboratory Managers, Regeneron Regulatory Sciences, Regeneron Procurement, Regeneron Warehouse and Logistics (WHL), Regeneron Protein Group in Tarrytown, and partners. As a QC Analyst you will culture customer service for all internal and external clients. As a Quality Control Analyst - Materials, a typical day might include the following: Responsible for QC Reference Standard and Materials processes. Sets and maintains internal requirements for product reference standards. Ensures timely procurement and implementation of product reference standards and qualified materials. Oversee and maintain appropriate inventory levels of product reference standards and qualified materials. Work with members of QC Labs, Tarrytown, and Business Partners for reagent and product reference standard forecasts. Provide excellent customer service. Evaluates and documents deviations in the appropriate Quality System. Oversight of the preventive and corrective maintenance monitoring program. Prepare and provide regular data updates to the management and group. Lead and coordinate the improvement effort of streamlining processes. This role might be for you if : Data analysis using excel spreadsheets or other software applications. You can work independently and drive projects to completion. You have a passion for technical writing and excel at quickly understanding and interpreting complex or new information. You can adhere to established procedures. You can collaborate effectively with people who may not be on your immediate team and willing to ask others for information. Are familiar with GMP(good manufacturing practices) and GDP (good documentation practices). You can work independently and drive projects to completion. You can work in a hood in a lab and utilize a pipette. To be considered for the Quality Control Analyst on the Materials team you must be willing and able to work Monday-Friday, 8am-4:30pm.

Requirements

• BS/BA in Biology, Chemistry, Biochemistry or related Life Sciences field; or an equivalent combination of education and experience
• 12-18+ months of related experience
• Data analysis using excel spreadsheets or other software applications.
• You can work independently and drive projects to completion.
• You have a passion for technical writing and excel at quickly understanding and interpreting complex or new information.
• You can adhere to established procedures.
• You can collaborate effectively with people who may not be on your immediate team and willing to ask others for information.
• Are familiar with GMP(good manufacturing practices) and GDP (good documentation practices).
• You can work independently and drive projects to completion.
• You can work in a hood in a lab and utilize a pipette.

Responsibilities

• Responsible for QC Reference Standard and Materials processes.
• Sets and maintains internal requirements for product reference standards.
• Ensures timely procurement and implementation of product reference standards and qualified materials.
• Oversee and maintain appropriate inventory levels of product reference standards and qualified materials.
• Work with members of QC Labs, Tarrytown, and Business Partners for reagent and product reference standard forecasts.
• Provide excellent customer service.
• Evaluates and documents deviations in the appropriate Quality System.
• Oversight of the preventive and corrective maintenance monitoring program.
• Prepare and provide regular data updates to the management and group.
• Lead and coordinate the improvement effort of streamlining processes.

Benefits

• health and wellness programs (including medical, dental, vision, life, and disability insurance)
• fitness centers
• 401(k) company match
• family support benefits
• equity awards
• annual bonuses
• paid time off
• paid leaves (e.g., military and parental leave)

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Number of Employees: 5,001-10,000 employees