QC Analyst, Life Sciences — GMP & On‑Site Role

Regeneron Pharmaceuticals, Inc (USA); United States; On-site; USD 52,000 - 92,000; 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, Inc. in Saratoga Springs, NY is hiring multiple Quality Control Analysts to support our new fully automated drug substance manufacturing facility.

The role involves performing chemical, biological, and microbial analyses across raw materials, in-process materials, products, and stability samples to support quality programs. Initial location is Rensselaer, NY with permanent on-site work in Saratoga Springs; shifts include 1st shift Mon-Fri and rotating 12-hour

Qualifications

• Requires B.S in Life Sciences or related field.
• Associate Quality Control Analyst: 0-2 years of experience.
• Quality Control Analyst: 2+ years of experience.
• Senior Quality Control Analyst I: 4+ years of experience.

Responsibilities

• Gather data and documents test results.
• Review test results for compliance and report quality anomalies.
• Comply with all pertinent regulatory agency requirements.
• Participate in GMP training activities.
• Maintain laboratory supplies.
• Conduct testing and sampling on raw materials, in-process, product, stability, and research samples.
• Write and revise control test procedures and 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

B.S in Life Sciences or related field

Job description

Regeneron Pharmaceuticals, Inc. in Saratoga Springs, NY is hiring multiple Quality Control Analysts to support our new fully automated drug substance manufacturing facility.

The role involves performing chemical, biological, and microbial analyses across raw materials, in-process materials, products, and stability samples to support quality programs. Initial location is Rensselaer, NY with permanent on-site work in Saratoga Springs; shifts include 1st shift Mon-Fri and rotating 12-hour