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Materials Planning Specialist - External Manufacturing

Employer
Regeneron Pharmaceuticals, Inc.
Location
Troy, New York
Start date
Aug 4, 2022

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Job Details

We are currently looking to fill a Materials Planning Specialist position. The Materials Planning Specialist-External Manufacturing is a key member of an External Manufacturing Team who collaborates with various departments and manufacturing partners to ensure on-time delivery of materials and on-time production and release of parenteral medicines. This role works with minimal supervision, proactively identifies and resolves issues that could impact production schedules and is capable of identifying and implementing meaningful change.

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

  • External Manufacturing subject matter expert for Oracle to process CMO Quotes (Project Plans/Work Orders) and invoices, tracking the status of PO approval.
  • Maintains critical databases and ensures accuracy and integrity of the data.
  • Generates reports necessary to manage production activities and provides input on key decisions.
  • Ensure accessible history of allocations, knowledge of material consumptions and calculates manufacturing yields in Oracle and other designated systems.
  • Tracks, trends and monitors a wide variety of External Manufacturing data; prepares reports analyzing data and makes recommendations proactively with minimal supervision.
  • Collaborates directly with CMOs and relevant internal stakeholders to resolve errors and questions on invoices.
  • Leads and supports Continuous Improvement initiatives to improve efficiency and quality of processes and operations.
  • Identifies problems and takes the initiative to resolve them.
  • Collaborates with relevant internal stakeholders in coordinating shipments and ensures on-time deliveries.
  • Participates in key projects with the expectation to lead initiatives with increased importance to the EM organization.
  • Supports investigations if needed in accordance with Regeneron requirements.
  • May travel to contractor sites (>10%).

This role may be for you if you:
  • Proficient in Excel, PowerPoint, Word, etc. in addition to experience working within shared work environments (i.e. SharePoint, Box, eRoom).
  • Exhibits confidence and has strong interpersonal, written and oral communication skills for providing team updates.
  • Gains understanding from provided instructions and works towards goals with minimal supervision.
  • Experience working within GMP/Quality systems. Oracle
  • Exhibits a degree of ingenuity, creativity and resourcefulness in evolving and ambiguous environments.
  • Understands and listens to team members and stakeholders needs while supporting productive team environments toward one common objective.
  • Shows flexibility and willingness to collaborate in the face of challenges and adversarial situations.
  • To be considered for this role you must hold A
  • Associate Specialist: Requires BS/BA or equivalent combination of education and experience.
  • Specialist: Requires BS/BA and 2 years of related experience in cGMP manufacturing operations (clinical and/or commercial External Manufacturing) or equivalent combination of education and experience.
  • Senior Specialist: Requires BS/BA and 5 years of related experience in cGMP manufacturing operations (clinical and/or commercial External Manufacturing) or equivalent combination of education and experience

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 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.

Company

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

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Company info
Website
Phone
914-847-7000
Location
Corporate Headquarters
777 Old Saw Mill River Road
Tarrytown
New York
10591
United States

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