As a Lead QC Lab Instrumentation Analyst you would support the Quality Control (QC) and Process Sciences (PS) departments by maintaining their laboratory instrumentation in an operational, qualified state. This entails ensuring both instrument hardware and software qualifications are completed in a timely manner and keeping them in a qualified state.

Lead-Related Activities include, but are not limited to, the following:

Providing on-the-floor guidance and support to team membersEnsuring that the team’s timesheets are completed on timeMonitoring training to ensure that all requirements are met, including OJT.Maintaining up to date training records for self and direct reportsPerforming monthly performance feedback meetings with direct reportsEscalating all performance issues to management and/or HRScheduling and coordinating workload of the teamProjecting managing activities associated with the group

A typical day might include, but is not limited to, the following: 

Overseeing and managing equipment activities including but not limited to performing maintenance, repairing, relocating, and decommissioning.Facilitating all lifecycle activities in a timely manner to enable QC laboratories to execute their functions.Coordinationing of lab equipment sustaining programCoordinationing of activities relating to the calibration and maintenance of laboratory equipment and related systems.Scheduling and coordinating all preventive maintenance and repair work performed by outside contractors (includes ensuring vendors are in compliance with site requirements prior to performing equipment related services).Reviewing of vendor documentation in support of preventative maintenance, calibration and repair work including maintaining the ASL and resulting SLA’Communicating and coordinate with other departments or outside contractors/vendors to complete equipment related tasks and/or resolve issues.Ensuring calibration, maintenance and repair activities are communicated to and scheduled with the affected QC functional area and that the area manager(s) is informed.Ensuring the timely submission of work order requests for QC equipment and that scheduled work is completed appropriately.Supporting change control activities impacting QC equipment; provide impact assessments when required.Performing investigations of equipment related deviations as needed.Participating in Lab Maintenance activities as needed.Supervising technicians working to support QC equipment lifecycle activities.Serving as principal contact for QC equipment.Complying with all pertinent regulatory agency requirements.Writing and revise Equipment related SOPs as necessary

This role might be for you if:

You have current or prior experience working with instruments in a regulated environmentYou have a proven ability to work independently or as part of a teamYou possess strong trouble-shooting and problem solving skillsYou have strong attention to detail and excellent written and oral skills

To be considered for this opportunity you should hold a BS/BA in Chemistry, Life Sciences, Engineering, or related field preferred; will substitute relevant experience for education

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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.