S

Société Générale de Surveillance

Testing, inspection, and certification services globally

Quality and Regulatory Specialist - Flamability Lab

Validation, Compliance & Quality SystemsConfirmed live in the last 24 hours
Full-timeFarmingdale, NY, USAIn-person

About the Job

Requirements

  • A high school diploma or equivalent is required.
  • A minimum of 5 years of relevant experience is required.
  • The ability to manage and coordinate multiple projects in a fast-paced, highly professional environment is required.
  • Familiarity with jurisdictional and ISO requirements is required.

Responsibilities

  • Maintain knowledge of Good Clinical Practices, Good Laboratory Practices, ISO 17025:2017, Standard Operating Procedures, and applicable federal regulations.
  • Review protocols, informed consents, and case report forms before study initiation and review revised documents.
  • Review company policies and procedures to ensure they meet regulatory standards.
  • Collaborate with operational teams to incorporate regulatory compliance into design processes and delivery scope.
  • Prepare and submit documentation to regulatory agencies and accrediting bodies as needed.
  • Stay up to date with changes in regulatory legislation, guidelines, and industry standards.
  • Monitor and set standards for quality control.
  • Investigate and set standards for safety and health.
  • Assess outcome, compliance, and operational risks and develop risk management strategies.
  • Conduct internal audits to measure and assure adherence to established quality assurance standards in accordance with applicable regulations and guidelines.
  • Train staff and team members on quality, regulatory, and compliance issues.
  • Maintain and organize necessary documentation.
  • Address non-compliance issues.
  • Work directly with international coordinators and project managers to ensure accurate client documentation.
  • Conduct audits of clinical trial master files, source data, and procedures for protocol, monitoring plan when applicable, Standard Operating Procedures, and Good Clinical Practice/International Council for Harmonisation compliance.
  • Assist with auditing company training files.
  • Assist with documenting root-cause analyses arising from internal non-conformances, corrective actions, and preventive actions.
  • Assist in reviewing clinical study protocol deviations.
  • Train new departmental staff.
  • Perform other duties or tasks assigned by a manager or supervisor.
  • Encourage prompt reporting of health and safety concerns.

Desired Qualifications

  • An Engineering Technology Diploma is preferred.
  • Supervisory experience is an asset.
  • Good organizational and time-management skills.

About the Company

Société Générale de Surveillance

Testing, inspection, and certification services globally

SGS provides testing, inspection, and certification services to help clients meet regulations, ensure quality and safety, and gain market access. It runs laboratory testing, on-site inspections, and certification against standards, often with training and consulting, across a wide range of industries. The services rely on a global network of laboratories and offices that deliver localized solutions with global expertise. What sets SGS apart is its large global footprint and its emphasis on quality, integrity, risk mitigation, and sustainability, enabling it to serve a diverse set of customers from small businesses to multinationals. The company's goal is to help customers comply with regulations, improve product quality and safety, reduce risk, and boost productivity across markets.

Company size
10,001+
Company stage
IPO
Headquarters
Geneva, Switzerland
Founded
1878

Recently Posted Jobs

Explore more opportunities at Société Générale de Surveillance

See more jobs