Quality Control Technical Resources Specialist

Posted 13 Hours Ago
Be an Early Applicant
Rensselaer, IN
66K-127K Annually
Mid level
Biotech • Pharmaceutical
The Role
As a Quality Control Technical Resources Specialist, you will manage validation and qualification projects, collaborate with teams, write protocols, control test procedures, and communicate with management and partners on progress and discrepancies. You will thrive in a fast-paced environment, handling multiple tasks and driving scientific improvements.
Summary Generated by Built In

We are currently looking to fill a Technical Resources Specialist part of our QC Technical Resources Chemistry 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.

As a 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 be willing and able to work Monday-Friday, 8am-4:30pm. You must have a BS/BA in Chemistry, Biochemistry, Biology or related field with 3+ 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 have an inclusive and diverse culture that provides comprehensive benefits, which often include (depending on location) health and wellness programs, fitness centers, 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. The Company will also provide reasonable accommodation to the known disabilities or chronic illnesses of an otherwise qualified applicant for employment, unless the accommodation would impose undue hardship on the operation of the Company's business.

For roles in which the hired candidate will be working in the U.S., the salary ranges provided are shown in accordance with U.S. law and apply to U.S.-based positions. For roles which will be based in Japan and/or Canada, the salary ranges are shown in accordance with the applicable local law and currency. If you are outside the U.S, Japan or Canada, please speak with your recruiter about salaries and benefits in your location.

Please note that certain background checks will form part of the recruitment process. Background checks will be conducted in accordance with the law of the country where the position is based, including the type of background checks conducted. The purpose of carrying out such checks is for Regeneron to verify certain information regarding a candidate prior to the commencement of employment such as identity, right to work, educational qualifications etc.

Salary Range (annually)

$66,400.00 - $126,800.00

The Company
HQ: New York, New York
15,000 Employees
Hybrid Workplace
Year Founded: 1988

What We Do

At Regeneron we believe that when the right idea finds the right team, powerful change is possible. As we work across our expanding global network to invent, develop and commercialize life-transforming medicines for people with serious diseases, we’re establishing new ways to think about science, manufacturing and commercialization. And new ways to think about health. Connect with us so we can learn more about you, and you can learn more about our biopharmaceutical medicines. And join us, as we build a future we believe in.

Please visit www.regeneron.com/social-media-terms for information on how to engage with us on social media.

An important note about privacy: Regeneron is committed to your privacy and will not ask for sensitive personal information such as social security number, date of birth or bank account details via email or social media.

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