Skip to main content

This job has expired

You will need to login before you can apply for a job.

QA Specialist (MES) - Fill Finish

Regeneron Pharmaceuticals, Inc.
East Greenbush, New York
Start date
Feb 10, 2024

View more

Clinical, Clinical Medicine, Quality
Required Education
Bachelors Degree
Position Type
Full time
Pharm Country, Best Places to Work

Job Details

We are currently looking to fill a Quality Assurance Specialist position to support the Manufacturing Execution System (MES). This position will support a cross functional team of MES Specialists by providing a QA perspective with regards to manufacturing business processes, documentation requirements, and overall design of records. We are looking for someone who can continuously provide QA input and feedback in accordance with regulations, policies and procedures.

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

Reviewing company documentation including SOPs, SPECS, Process Transmittals, and Manufacturing Batch Records to assess MES impact
Identifying difficulties and suggesting alternatives that are aligned with QA
Reviewing MES change controls and test plans
Working with Technical Trainers to develop QA training plans for MES users
Collaborating in the creation, review, and approval of validation documents
Reviewing and approving MES recipes, design specifications, master batch records, and electronic records to meet the requirements of manufacturing and QA users
Supporting Pre-Production Executions (Pre-PE) and delivering feedback
Providing end-user support for MES usage and working closely with IT to troubleshoot problems associated with QA functions
Support/lead efforts to establish new programs including start-up of formulation, filling, inspection, assembly, and pack and label team
Perform assessments of existing procedures/documents to gauge appropriateness for the inclusion of drug product operations; where current documents are not adequate, identify path forward for establishment of procedures
Develop, write, review, and approve SOPs, specifications, and other documents. This includes documents for operation and facility SOPs, quality training, batch documentation, etc.
Accountable for maintaining project timelines associated with quality assurance initiatives
Perform On-The-Floor quality review of documents
Review and approval of documents including executed Batch Records and SOPs (electronic and paper-based)
Execute daily operations per strategic direction in a multifaceted environment.
Provide mentorship during on-the-floor manufacturing
Support audits, inspections and investigations.

This role may be for you if you:

You have previous QA operations experience, particularly with batch record review / MES design, implementation or training
You are a strong communicator and can use effective communication while collaborating with other functions
You are driven and self-motivated
You seek out new ways to improve processes and make changes accordingly
You enjoy project work in a fast paced, startup type environment

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

Assoc QA Specialist 2+ years
QA Specialist 4+ years

Sr QA Specialist 6+ years

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


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 comprehensive benefits including health and wellness programs, fitness centers and 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. 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.

The salary ranges provided are shown in accordance with U.S. law and apply to U.S. based positions, where the hired candidate will be located in the U.S. If you are outside the U.S, please speak with your recruiter about salaries and benefits in your location.

Salary Range (annually)

$58,480.40 - $124,300.00


Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led for 30 years by physician-scientists, our unique ability to repeatedly and consistently translate science into medicine has led to seven FDA-approved treatments and numerous product candidates in development, all of which were homegrown in our laboratories. Our medicines and pipeline are designed to help patients with eye disease, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, infectious diseases, pain and rare diseases.
Regeneron is accelerating and improving the traditional drug development process through our proprietary VelociSuite® technologies, such as VelocImmune® which produces optimized fully-human antibodies, and ambitious research initiatives such as the Regeneron Genetics Center, which is conducting one of the largest genetics sequencing efforts in the world.

Stock Symbol: REGN

Stock Exchange: NASDAQ

FacebookTwitterInstagramYouTube Logo

Company info
Corporate Headquarters
777 Old Saw Mill River Road
New York
United States

Get job alerts

Create a job alert and receive personalized job recommendations straight to your inbox.

Create alert