Regeneron Pharmaceuticals, Inc

Process Development Engineer II, Analytics: Synthetic and Bioconjugation Scale-Up Technologies (SBST)

Regeneron Pharmaceuticals, Inc$93K — $153K *
Pharmaceuticals & Biotech
Less than 5 years of experience
Job Overview by Ladders

Qualifications

  • B.S. with 6+ years or M.S. with 4+ years in relevant scientific fields.
  • Hands-on experience in analytical method development for synthetic molecules.
  • Proficiency in techniques like HPLC, MS, UV spectroscopy, and associated software.
  • Experience in transferring methods and troubleshooting within development labs.
  • Strong written and verbal communication skills for diverse audiences.

Responsibilities

  • Design and execute analytical testing for bioconjugate development.
  • Compile and interpret complex datasets for actionable insights.
  • Lead analytical deliverables and coordinate with internal/external teams.
  • Provide technical support and troubleshoot analytical activities.
  • Author documentation to support program timelines.
  • Improve workflows for documentation and data management.
  • Train and mentor team members as necessary.

Benefits

  • Access to continuous learning and development programs.
  • Collaborative and innovative work environment.
  • Opportunities for career advancement.
  • Support for work-life balance with flexible scheduling.
Full Job Description
Regeneron's Preclinical Manufacturing & Process Development (PMPD) organization in Tarrytown, NY is seeking a highly motivated Process Development Engineer II to join our Synthetic and Bioconjugation Scale-up Technologies (SBST) Analytics group. In this role, you will serve as the analytical lead to develop fit-for-purpose analytical methods to characterize critical intermediates (small molecules, siRNA, and/or peptides) to support our growing and diverse bioconjugate pipeline. You will lead and implement analytical deliverables working closely with cross-functional teams and external collaborators (CDMOs) to advance bioconjugate programs from development to commercialization.

A Typical Day in the Role of Process Development Engineer II Might Look Like:

  • Design and execute analytical testing, method development and characterization of critical intermediates to enable bioconjugate development.
  • Compile, analyze, and interpret complex datasets; connect key findings across experiments and propose clear, actionable next steps.
  • Communicate results and recommendations clearly to technical and non-technical audiences to enable timely, data-driven decisions.
  • Serve as the analytical lead for critical intermediates and bioconjugates; coordinate internal and external analytical deliverables (development, transfer, and troubleshooting) to support program milestones.
  • Provide technical support and troubleshooting to receiving labs to keep analytical activities off the critical path.
  • Author high-quality documentation (e.g., procedures, method development reports, characterization reports, ELN entries) to support program timelines.
  • Build and improve business workflows for documentation standardization, data digitization, and sample management.
  • Maintain compliance with lab and environmental safety and promote a safe lab culture.
  • Support equipment upkeep, troubleshooting, maintain an organized workspace, and proactively plan for lab resources.
  • Train and mentor peers and junior team members as needed (directly and/or indirectly).


This Role May Be For You If You:
  • Enjoy hands-on lab work and consistently generate high-quality, reproducible data.
  • Take initiative, deliver on challenging work, and learn new technologies quickly.
  • Have hands-on experience with analytical techniques for synthetic molecules (i.e., peptide, siRNA, and small-molecule) characterization and relevant software's.
  • Possess a customer-centric mindset to analytical development and understand how analytical deliverables enable program decisions across drug development in different phases of the program
  • Thrive in a fast-paced, highly collaborative environment working on complex problems.
  • Communicate clearly (written and verbal), simplify messages for impact, and build strong working relationships.
  • Think critically and apply strong problem-solving skills, and comfortable navigating ambiguity.


This role requires B.S. with 6+ years of relevant experience, or M.S. with 4+ years of relevant experience, in analytical chemistry, biochemistry, biology, chemical engineering, or a related field. Hands-on experience with analytical method development for synthetic molecules (e.g., small molecules, PEG, peptides, and/or oligos), i.e. electrophoresis, HPLC, MS, UV spectroscopy and associated software (e.g., Empower). Experience transferring methods to internal/external development labs, and troubleshooting. Demonstrated experience serving as an analytical lead, working with internal teams and external CDMOs. Strong written and verbal communication skills, including the ability to present data clearly to diverse audiences. Ability to work with minimal guidance and collaboratively across cross-functional teams, with strong attention to detail and documentation practices. Demonstrated initiative, learning agility, and a growth mindset in a fast-paced environment. Experience with antibodies and/or bioconjugates is strongly preferred.

#pmpd

Salary Range (annually)

$93,900.00 - $153,300.00

About Regeneron Pharmaceuticals, Inc

Regeneron Pharmaceuticals is a biopharmaceutical company that discovers, develops, and commercializes pharmaceutical products for the treatment of serious medical conditions. The Company has therapeutic candidates in clinical trials for the potential treatment of cancer, eye diseases, and inflammatory diseases, and has preclinical programs in other diseases and disorders. The company’s product portfolio includes EYLEA, an aflibercept injection; ARCALYST, a rilonacept Injection for subcutaneous use; ZALTRAP for metastatic colorectal cancer; trap fusion proteins; and fully human monoclonal antibodies. On March 26, 2012, it was announced that Sanofi and Regeneron are in development with a new cholesterol drug which will help reduce cholesterol up to 72%. Regeneron Pharmaceuticals was founded in 1988 and is currently headquartered in New York, USA.

Regeneron Pharmaceuticals, Inc Careers

Join the innovative team at Regeneron Pharmaceuticals, Inc, a leading biotechnology company renowned for its commitment to science-driven solutions. This is an unparalleled opportunity to advance your career with a company at the forefront of medical breakthroughs and clinical research.

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Lead the way in biotechnological innovation with Regeneron. Our leadership is constantly looking towards the future, investing in cutting-edge technology and research that pave the way for medical advancements. At Regeneron, leadership and innovation go hand in hand, creating a dynamic where breakthroughs are common.

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Learn more about Regeneron Pharmaceuticals, Inc
Size
10,368 employees
Market Cap
$78.1 billion
Industry
Net Income
$3.5 billion
Founded
1988
5 Year Trend
+27%
Revenue
$8.4 billion
NASDAQ

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