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Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Analytical Technology & Operations Specialist

Regulatory & Quality (Life Sciences)Updated on Nov 11
Full-timeRensselaer, NY, USA$62.4k - $131.3k /yr

About the Job

Requirements

  • A BS/BA in Engineering, Chemistry, or Life Sciences is required, though relevant experience may substitute for education.
  • Relevant experience requirements vary by level: Associate Specialist requires 0–2+ years; Specialist requires 2+ years; Senior Specialist requires 5+ years.
  • Familiarity with data integrity principles (ALCOA+), 21 CFR Part 11, Annex 11, and GxP requirements, with an ability to apply them under guidance.

Responsibilities

  • Gather and document assay-to-space model inputs for the assigned area, including equipment lists, footprint measurements, and bench linear feet.
  • Support development of User Requirement Specification content by documenting equipment and network/instrument integration details, and escalate integration decisions.
  • Maintain integration documentation for laboratory systems connecting to the lab bus, and flag data integrity or control gaps.
  • Document material, sample, and personnel flow for the assigned area from receipt through login, preparation, analysis, retain, and waste, based on approved process maps.
  • Support data integrity risk and gap assessment activities by collecting evidence, completing checklists, and organizing findings for the Senior Specialist’s review.
  • Prepare supporting materials and impact documentation for design reviews and proposed value-engineering changes.
  • Coordinate day-to-day logistics for instrument delivery, installation, and FAT/SAT activities against the first test-date schedule.
  • Execute qualification protocols and pre-defined acceptance-criteria testing for laboratory-critical functionality.
  • Support LIMS configuration and laboratory digital integration tasks.
  • Assist in maintaining integration requirement documentation for lab bus-connected systems and escalate design-versus-installation discrepancies.
  • Draft and revise SOPs for the assigned space, covering access and gowning, sample receipt and handling, instrument operation, cleaning and sanitization, waste, cold chain, and retain management.
  • Participate in and help execute dry runs of the sample-to-result path, and support engineering runs for the assigned area.
  • Provide day-to-day post-handover support to the site QC testing team by triaging routine issues, helping execute change control and corrective actions, and escalating complex or ambiguous issues to the Senior Specialist.

Desired Qualifications

  • Exposure to laboratory system integration, including CDS, LIMS, instrument interfacing, or networked data acquisition.
  • Exposure to a laboratory build, relocation, fit-out, or instrument implementation project.

About the Company

Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Regeneron Pharmaceuticals develops and commercializes medicines for serious diseases, with a focus on cancer, eye diseases, allergic and inflammatory diseases, and infectious diseases. Its products come from using proprietary research capabilities and technologies to discover and develop therapies, often in collaboration with academic, research, and industry partners. Revenue comes from selling approved medicines and from licensing its technologies and entering co-development and co-commercialization partnerships. The company works with healthcare providers and regulators to ensure treatment delivery and safety. Its goal is to improve patient outcomes by bringing life-transforming medicines to market through rigorous R&D and strategic collaborations, maintaining leadership in biopharmaceutical innovation.

Company size
10,001+
Company stage
IPO
Headquarters
Town of Mount Pleasant, New York
Founded
1988

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