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We are currently looking to fill a QA Inspection Specialist position. This position will support Visual Inspection operations performed at Regeneron’s Internal Fill/Finish facility. This position will provide floor support during production activities and also contribute to establishing/updating procedures and policies to ensure assigned areas are operating to current FDA and International Regulatory Body requirements.

Available Working Schedules:

• Monday-Friday, 2nd shift (2p-10:30p)

• Monday-Friday, 1st shift (10a-6:30p)

In this role, a typical day might include the following:

• Oversee programs to support Visual Inspection Operations at the Drug Product facility.

• Ensure that facilities, equipment, materials, processes, and procedures comply with applicable regulations and requirements relating to Good Manufacturing Practices, Good Documentation Practices, Safety, and other Regeneron controls.

• Execute daily operations, including, but limited to:

• Providing Quality Oversight and guidance during on-the-floor manufacturing

• Executing daily on-the-floor duties to ensure facilities, equipment, materials, and documentation comply with SOPs and safety standards.

• Performing Quarantine and Segregation of material.

• Performing line clearances activities.

• Perform Acceptable Quality Level (AQL).

• Review and approve procedures, documents and records, including but not limited to Batch Production Records, and Protocols.

• Ensure that EBR/Batch Records are complete, accurate, and documented according the written procedure.

• Quality support in electronic batch record creation, review, and approval.

• Author/Review/Approve Quality documents, such as Standard Operating Procedures (SOP’s), Risk Assessment (RA), training materials, training documents, protocols and reports.

• Support and represent QA during audits and inspections; may directly interact with regulatory agencies during on-site inspections.

• Identification and implementation of continuous improvement opportunities within our processes and systems and contribute to the continuous improvement culture.

• Maintain project timelines associated with initiatives to support the evolving business.

This role may be for you if you:

• Must pass a visual acuity exam, including color assessment.

• Must successfully complete the visual inspection training and qualification program.

• Capable of building strong interpersonal skills with ability to collaborate on cross functional teams.

• Demonstrate ability in problem solving.

• Strong organizational skills, including to follow assignments through to completion.

• Ability to work in a fast-paced and dynamic environment.

• Apply critical thinking skills to ensure quality and compliance to GMP regulations for all area operations and associated processes.

To be considered for this role you must hold a Bachelor’s degree in Life Sciences or related field and the following minimum amounts of relevant experience for each level:

• Assoc Specialist – 2+ year

• Specialist – 4+ years

• Senior Specialist – 6+ years

May substitute proven experience for education requirement. Level is determined based on qualifications relevant to the role.

#REGNQA

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)

$58,480.40 - $124,300.00