Quality Control Analyst — Cleanroom Lab, On-Site & Growth

Regeneron Pharmaceuticals; Saratoga Springs (UT); On-site; USD 34,000 - 61,000; Full time

Benefits offered by this job

Student loan paydown program & tuition

Family care benefits

Relocation assistance

Inclusion, culture and well-being

Job summary

Regeneron Pharmaceuticals in Saratoga Springs, NY, is hiring multiple Quality Control Analysts to perform chemical/biological analyses in a state-of-the-art facility. The role requires a B.S in Life Sciences and 0–8+ years of experience, with on-site work and rotating schedules as applicable.

You will collect and review test data, ensure regulatory compliance, participate in GMP training, and help develop analytical methods while supporting transfer from R&D.

Qualifications

• Requires B.S in Life Sciences or related field; or equivalent combination of education and experience
• Level will be determined based on experience

Responsibilities

• Gather data and documents test results
• Review test results to ensure compliance with standards; reports any quality anomalies
• Comply with all pertinent regulatory agency requirements
• Participate in required GMP training activities
• Maintain laboratory supplies
• Conduct testing and sampling on raw materials, in-process, product, stability, and/or research samples
• Write and revise control test procedures and standard operating procedures (SOPs)
• Complete test records and reviews data
• Calibrate or verify calibration of instruments/devices prior to use
• Interact with outside customers or functional peer groups
• Engage in exciting projects aligning to our scientific initiatives
• Devise or develop new analytical methods and techniques
• Assist in validation of methods
• Partner with internal teams on establishing the transfer of methodology from R&D

Education

BS in Life Sciences

Job description

Regeneron Pharmaceuticals in Saratoga Springs, NY, is hiring multiple Quality Control Analysts to perform chemical/biological analyses in a state-of-the-art facility. The role requires a B.S in Life Sciences and 0–8+ years of experience, with on-site work and rotating schedules as applicable.

You will collect and review test data, ensure regulatory compliance, participate in GMP training, and help develop analytical methods while supporting transfer from R&D.