We are currently looking to fill a Technical Resources Specialist within our Quality Control team. This position is a Monday-Friday 8am-4:30pm schedule. 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.
As an QC Technical Resources Specialist, a typical day might include the following
- 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.
This role might be for you if you:
- Enjoy working in a fast-paced environment.
- Are able to multi-task, prioritize and execute projects independently
- Are able to write and review transfer documents such as protocols and reports
- Enjoy and are able to communicate cross-functionally to business units.
- Can take on new and sometimes ambiguous challenges and learn quickly.
- 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).
To be considered for the QC Technical Resources Specialist position you must have a BS/BA in Chemistry, Biochemistry, Biology, or related field, with 2+ years of experience. Experience with project management and experience in a GMP setting is preferred.
Level is determined based on qualifications relevant to the role.
Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture.
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 additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/. For other locations, additional information will be provided during the recruitment process. If you have any questions, please speak with your recruiter.
Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed onsite. Please speak with your recruiter and hiring manager for more information about onsite expectations for your role and location.
Salary Range (annually)
$67,400.00 - $110,000.00
