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Regeneron Pharmaceuticals

Project Specialist Quality Control

Regeneron Pharmaceuticals

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  • Date Posted

    Today

    New!
  • Remote Work Level

    Hybrid Remote

  • Location

    Hybrid Remote in Rensselaer, NY

  • Job Schedule

    Full-Time

  • Salary

    $67,400 - $110,000 ANNUALLY

  • Benefits

    401k Matching/Retirement Savings Dental Insurance Disability Insurance Health/Medical Insurance Life Insurance Vision Insurance Paid Vacation Parental and Family Leave Health & Wellness Programs

  • Categories

    Product Manager,  Project Manager,  Chemistry

  • Job Type

    Employee

  • Career Level

    Experienced

  • Travel Required

    No Specification

  • Education Level

    Bachelor's/Undergraduate Degree

About the Role

Project Specialist Quality Control

remote type

Hybrid

locations

RENSSELAER

time type

Full time

We are currently looking to fill a Project Specialist on our Quality Control Technical Resources Team. This position will be supporting project management of validation and qualification activities, transfer to partner and contract sites, and life cycle management of assays utilized in Quality Control testing. Regeneron has successfully commercialized numerous products and in this fast-paced environment with a strong pipeline, QC Technical Resources Specialists have the opportunity to develop scientifically and also gain insight into other areas of the business.

When & Where:

  • Monday–Friday, 8:00am–4:30pm
  • Location: Rensselaer, New York, United States

Discover your role:

  • Project manage validation and qualification activities within the QC TR Chemistry group
  • Collaborate with internal and external teams to coordinate project management activities
  • Write and revise assay transfer protocols to external partners and contract labs
  • Write and revise control test procedures and SOPs
  • Coordinate and participate in weekly project update meetings
  • Communicate to management any delay in validation/transfer timelines
  • Communicate method updates to partners and manage progress of updates
  • Coordinate post-transfer investigations between contract sites and collaborative partners
  • Raise discrepancies to management, as needed
  • Multi-task, prioritize and execute projects independently 
  • Write and review transfer documents such as protocols and reports
  • Communicate cross-functionally to business units
  • Develop and drive scientific and/or business-related improvement ideas
  • Possess effective time management skills, and the drive to meet deadlines
  • Have working knowledge of Microsoft Suite (Word, Excel, Powerpoint)

This role requires:

A BS/BA in Chemistry, Biochemistry, Biology or related field, with 3+ years of relevant experience.

Experience with project management and experience in a GMP setting.

Level is determined based on qualifications relevant to the role.

Where necessary, we disclose salary ranges for roles in all countries in which we operate.  The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits.  Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits.

For jobs in Canada: this posting is for an existing position.

Salary Range (annually)

$67,400.00 - $110,000.00

Apply

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