Analytical Development Specialist at Regeneron Pharmaceuticals, Inc.

Regeneron is currently looking for an Analytical Development Specialist for our QC Analytical Sciences Bioassay team with a Monday-Friday, 8am-4:30pm schedule. The Analytical Development Specialist develops new Quality Control (QC) techniques and procedures for potency assays. Applies in-depth scientific knowledge to solve complex issues and advance the analytical strategy and technical capabilities of QC. Recognized Subject Matter Expert (SME) in QC. Incorporates new assays and techniques to increase efficiency or robustness of the analytical capabilities.

As an Analytical Development Specialist in the bioassay team, a typical day might include the following:

• Utilizes in-depth knowledge of state-of-the-art analytical instrumentation, methodology, and technology associated with developing MOA-reflective cell-based potency assays. Develops, writes and reviews protocols, reports and standard operating procedures at the qualification, validation, or transfer process.
• Applies a fundamental understanding of the science behind potency assays (mammalian cell culture, cell-based reporter assays, ELISA binding assays etc.) to perform advanced troubleshooting and complete complex analytical investigations.
• Owns or leads complex scientific projects or investigations.
• Independently designs and executes scientific experiments to assess new technology or troubleshoot and optimize existing assays. Assesses data and designs follow up experiments with no or limited supervision. May utilize statistical Design of Experiments (DOE) tools to streamline assay development and improve robustness.
• Stays current with industry trends in QC technology
• Proactively engages collaborators and equipment vendors to identify new technology and independently assesses the appropriateness of such technology for use in QC. Performs experiments using new technology as appropriate.
• Communicates clearly and effectively with management. Prepares thorough and clearly written scientific reports and standard operating procedures. Presents appropriate findings to management and group meetings.
• Readily shares information and willingly educates/trains other colleagues within and across departments.

This role might be for you if:

• Ability to make good and timely decisions. Proactively suggests experiments to management based on a broad and deep technical base.
• Leads by example and actively contributes to technical discussions.
• Seeks out opportunities and has a desire to learn both the technical aspects and IOPS culture;
• Meets commitments on time, safely, with quality
• Is a team player, is able to identify priorities within multiple tasks and is able to quickly transition and reprioritize when needed by the business.
• Is proactive in sharing knowledge and training others in multiple areas of expertise.
• Can independently design and execute complex scientific experiments to test hypothesis. Can analyze complex data and draw conclusions.
• Great written and oral communication skills

To be considered for the Analytical Development Specialist you must be willing and able to work Monday-Friday, 8am-4:30pm. For various levels you must have the following:

Associate Analytical Development Specialist: Requires a BS/BA in Life Sciences ; or equivalent combination of education and experience

Analytical Development Specialist: Requires a BS/BA in Life Sciences or related field and 2+ years of relevant experience; or equivalent combination of education and experience

Experience working in a cGMP/cGLP environment is preferred.

Experience with mammalian cell culture and cell-based potency assays is required.

Level is determined based on qualifications relevant to the role.

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 (annually)