Project Specialist Quality Control
About The Position
Regeneron is hiring a Project Specialist for its Quality Control Technical Resources Team. The position supports project management of validation and qualification activities, transfers to partner and contract sites, and life cycle management of assays used in Quality Control testing. The role offers opportunities to develop scientifically and gain insight into other areas of the business in a fast-paced environment with a strong product pipeline. The position is based in Rensselaer, New York, and is scheduled Monday through Friday from 8:00 a.m. to 4:30 p.m. The posting notes that many Regeneron roles are performed onsite; candidates should discuss specific onsite expectations with their recruiter and hiring manager. A bachelor's degree in Chemistry, Biochemistry, Biology, or a related field and at least three years of relevant experience are required. Experience in project management and a GMP setting is also required. The level will be determined based on qualifications relevant to the role.
Requirements
- Bachelor's degree in Chemistry, Biochemistry, Biology, or a related field.
- At least 3 years of relevant experience.
- Experience with project management.
- Experience in a GMP setting.
- Working knowledge of Microsoft Word, Excel, and PowerPoint.
- Effective time-management skills and ability to meet deadlines.
- Ability to multitask, prioritize, and execute projects independently.
Responsibilities
- Project-manage validation and qualification activities within the QC Technical Resources Chemistry group.
- Collaborate with internal and external teams to coordinate project management activities.
- Write and revise assay transfer protocols for external partners and contract laboratories.
- Write and revise control test procedures and standard operating procedures.
- Coordinate and participate in weekly project update meetings.
- Communicate delays in validation and transfer timelines to management.
- 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.
- Multitask, prioritize, and execute projects independently.
- Write and review transfer documents, including protocols and reports.
- Communicate cross-functionally with business units.
- Develop and drive scientific or business-related improvement ideas.
- Manage time effectively and meet deadlines.
Benefits
- Health and wellness programs
- Fitness centers
- Stock for employees at all levels
- Annual bonuses or other incentive plans may be included, depending on country and role
- Equity awards may be included, depending on country and role
- Pension or retirement benefits may be included, depending on country and role
- 401(k) company match may be included, depending on country and role
- Insurance benefits, including medical, dental, vision, life, and disability insurance, may be included, depending on country and role
- Paid time off may be included, depending on country and role
- Family support benefits may be included, depending on country and role
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
