R&D Associate (Quality Control)

Location
Tarrytown, NY, United States
Posted
Sep 15, 2020
Ref
20743BR
Discipline
Quality, Quality Control
Required Education
Bachelors Degree
Position Type
Full time
We are looking for an R&D Associate to perform a quality review of documentation that are routine in nature under the direct supervision of a supervisor/manager.

In this role, a typical day might include the following:
• Train, learn and follow established procedures and protocols to perform a quality review of routine assignments.
• Follow appropriate approaches or techniques to resolve findings, as directed.
• Collect and assemble all available resources to perform a quality review. Learns to evaluate the quality of documentation. May identify potential mistakes/issues that may result in a process improvement.
• Share information in a clear and transparent manner, and effectively take in information through strong listening skills. May participate in sub-group and/or department meetings and may share results of work with others.
• Demonstrates problem solving skills within defined procedures and practices to determine appropriate action. Learns to comfortably shift gears and priorities to meet changing needs as required.
• Executes vital operations in LIMS as needed and utilizes the ELN for documentation and review purposes.

This role may be for you if:
• You are a passionate learner who is open to feedback, learns from mistakes and participates in his/her own professional and personal development.
• You can optimally collaborate and engage with others while maintaining a productive working environment.
• You are willing to provide cross functional support when needed.
• You are able to begin to independently make detailed observations, interpret and report findings per defined procedures to team members and management.
• You can stay organized while multi-tasking across assignments and routinely performing high quality reviews.
• You possess knowledge of the basic principles of GxP, industry practices and standards.
• You can take direction and guidance from others in decision making.
• You act with integrity in all aspects of work to ensure ethical and professional conduct.

To be considered for this role, you must have ligand binding assay experience including ELISA, MSD, Gyros in GLP environment and/or protein biochemistry experience such as ELISA, chromatography (HPLC, FPLC), electrophoresis (SDS-PAGE, CE, Westerns, IEE), Mass Spectrometry and static or dynamic light scattering techniques. SoftMax Pro and Nautilus LIMS experience a plus. Computer proficiency including spreadsheets and databases is necessary. Proven understanding of Word and Excel required. Strong interpersonal and organization skills are required, as well as excellent communication skills (verbal and written.)

Does this sound like you? Apply now to take your first steps toward living the Regeneron Way! We have an inclusive and diverse culture that provides amazing benefits including health and wellness programs, fitness centers and stock for 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 maternity status, gender identity, gender reassignment, military or veteran status, or any other protected characteristic in accordance with applicable laws and regulations. We will ensure that individuals with disabilities are provided reasonable accommodations to participate in the job application process. Please contact us to discuss any accommodations you think you may need.