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Regeneron Pharmaceuticals

Develops biopharmaceutical therapies for serious diseases

Compliance Specialist - External Manufacturing

Regulatory & Quality (Life Sciences)Confirmed live in the last 24 hours
Full-timeEast Greenbush, NY, USA$62.4k - $128.7k /yr

About the Job

Requirements

  • A Bachelor of Science or Bachelor of Arts degree in a scientific field and related experience in current good manufacturing practice (cGMP) manufacturing operations: 0-2 years for Associate Specialist, 2 or more years for Specialist, or 5 or more years for Senior Specialist; level is determined based on experience.
  • Knowledge of drug product manufacturing from formulation through final packaging.
  • Basic knowledge of regulatory compliance, including cGMP, FDA regulations, familiarity with ICH guidelines, and European Union regulations.
  • Proficiency in Veeva, Opstrakker, Excel, PowerPoint, Visio, and Word, along with experience working in shared work environments.
  • Strong interpersonal, written, and oral communication skills, with an emphasis on technical writing.
  • Confidence and strong interpersonal and communication skills for providing team updates.
  • Resilience and flexibility when facing challenges and adversarial situations.
  • Ability to understand and listen to team members’ and stakeholders’ needs while supporting productive team environments toward a common objective.

Responsibilities

  • Lead and manage change controls, supplier corrective action requests (SCARs), SCNs, NPCs, and corrective and preventive actions (CAPAs).
  • Review and maintain procedures, policies, and other instructional documents, focusing on continuous improvement.
  • Maintain knowledge of current good manufacturing practices (cGMPs).
  • Support internal and external inspection and audit readiness activities.
  • Conduct periodic reviews of Drug Product Manufacturing documentation and records to assess compliance with established quality standards, policies, and procedures.
  • Maintain required training status on Regeneron-specific work instructions and standard operating procedures (SOPs).
  • Implement continuous process improvements.

Desired Qualifications

  • Experience collaborating with contract manufacturing organizations (CMOs) or contract research organizations (CROs).

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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