Quality Control Data Analyst

We are looking to hire a Quality Control (QC) Data Analyst for a 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 on the front line, performing a variety of activities to support release and stability programs of these life changing products to ensure that they are safe for our patients. 

As a Quality Control Analyst, a typical day might include the following:

• Compile internally and externally generated data in support of compiling CofAs and SofAs.
• Prepare and provide CofAs and SofAs for all lot release materials
• Work with members of manufacturing, QA, RA, and R/D to provide updates/status of CofAs, SofAs, testing issues, etc.
• Trend QC product release data to support lot release and regulatory filings

• Act as a liaison between QC, Process Analytical Sciences, and Manufacturing group to provide trending analyses to support various activities such as manufacturing investigations, and validation studies.
• Assist in the implementation and maintenance of product release and stability data trending program for each product candidate
•  Presents trending data at the in-depth product review
•  Write product annual release data trending reports
• Write lot specific data trending reports for each lot to be released
• Prepare and populate matrices (databases, spreadsheets) designed to track testing and review status of release and stability samples, lot release data, etc.
• Compile data to support QC department metrics and performance tracking
• Assist with the improvement effort of streamlining the review and release process
• Attend meetings as required on behalf of Quality Control to update partners (Drug Supply, External Manufacturing, QA) as to status issues pertaining to release data
• Attend meetings to keep informed of development and manufacturing priorities and activities
• Ensures compliance with applicable cGMP regulations and SOPs
• Maintain and update relevant SOPs for data review and reporting as needed
• Meet specified timelines to support release and regulatory filings
•  Complies with all pertinent regulatory agency requirements.
• Participates in required training activities.

This role might be for you if:

• Enjoy working in a fast-paced environment and you have the innate ability to balance multiple tasks, prioritize them and execute them independently, while excelling at keeping all impacted parties well advised
• Have a basic understanding of Microsoft Suite (Word, Excel, Powerpoint)
• Can follow a set of instructions with exceptional attention to detail
• Ability to work in a team environment and communicate effectively to accomplish shared goals
• Develop and drive scientific and/or business-related improvement ideas

To be considered for the Quality Control Analyst you must be willing and able to work 1st shift, Monday-Friday, 8am-4:30pm schedule. You must have a BS/BA in Chemistry, Biochemistry or related field and some relevant work experience. Experience working in a cGMP pharmaceutical Quality Control Laboratory is preferred but not required.

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, equity awards, annual bonuses, and paid time off for eligible employees at all levels!

Regeneron is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, nationality, national or ethnic origin, civil status, age, citizenship status, membership of the Traveler community, sexual orientation, disability, genetic information, familial status, marital or registered civil partnership status, pregnancy or parental status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.

For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions.  For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.

Please note that certain background checks will form part of the recruitment process.  Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.

Salary Range (hourly)