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MedPharm

Topical and transdermal drug delivery CDMO

Environmental Health & Safety Manager

Environmental Health & SafetyConfirmed live in the last 24 hours
Full-timeDurham, NC, USANo salary listedIn-person

About the Job

Requirements

  • A master's or bachelor's degree in EHS, Occupational Health, Engineering, Science, or a closely related discipline is desired, or equivalent technical experience plus demonstrated competence.
  • A minimum of 7 years of EHS-related experience within pharmaceutical manufacturing or R&D environments is required.
  • Demonstrated working experience implementing EHS regulations, conducting incident investigations, and interacting with regulatory agencies and external organizations.
  • Experience with pharmaceutical risk assessments and job hazard analysis.
  • Experience administering and ensuring compliance with DEA Controlled Substance licenses, including Schedule I through V compounds in a pharmaceutical research and manufacturing setting.
  • Familiarity with standard operating procedure authorship, change control systems, and document management practices as they apply to EHS program administration in a pharmaceutical contract research organization or R&D setting.
  • Demonstrated success exercising independent judgment, technical proficiency, and scientific creativity while collaborating with others in a current Good Manufacturing Practice environment.
  • Effective knowledge of applicable federal, state, and local regulations.
  • Familiarity with industry standards, including NFPA, ANSI, ACGIH, ISO, NIOSH, and ASME.
  • Familiarity with RCRA, CAA, CWA, NRC, EPA, DEP, and Residual Waste Regulations.

Responsibilities

  • Develop and maintain EH&S policies and procedures that comply with state, federal, and local regulatory requirements and company standards; implement compliant programs and procedures and assess their impact on affected areas.
  • Perform tasks across multiple EHS disciplines as needed and escalate compliance concerns to the management team based on risk exposure.
  • Analyze regulatory compliance data, including trends, and present it in management reviews.
  • Coordinate and conduct employee training in EH&S programs.
  • Coordinate and conduct safety inspections and audits, correlating inspection data with injury trends as needed.
  • Develop and manage an effective Emergency Response Program, including leading an Emergency Response Team.
  • Coordinate Occupational Health and Ergonomics Programs.
  • Coordinate with regulators, act as the primary contact at the sites, and follow appropriate escalation procedures.
  • Lead Material Risk Assessments for new compounds brought to any US site before they enter the facilities, and train affected individuals on safe handling.
  • Maintain records necessary to comply with local, state, and federal standards.
  • Define, report, and achieve EHS targets and key performance indicators.
  • Lead other professionals and management in applying standard EHS theories, concepts, and techniques.
  • Establish professional stakeholder relationships by developing rapport and understanding needs and shared goals.
  • Oversee accident and incident investigations and corrective actions.
  • Maintain EH&S training documentation so it is retrievable for client audits and regulatory inspections.
  • Guide the incident response team and Site Safety Committee.
  • Lead the site Hazardous Waste program and activities, and manage the introduction of new chemicals to the facility.
  • Lead regular site audits and risk assessments to ensure company and regulatory compliance; track and manage timely completion of corrective actions identified in audits or Failure Mode and Effects Analysis exercises.
  • Work with department leaders to develop and maintain safety training programs, ensuring training is documented, reviewed, effective, compliant, and timely.
  • At the R&D site, independently manage disposal of experimental compounds and study samples, including chain-of-custody documentation and client-specific destruction requirements consistent with records-retention standards.
  • Perform routine daily and weekly waste-management tasks, including biohazard waste pickups, chemical-waste container management and pickups, broken-glass disposal, and oil-waste collection.
  • Conduct routine safety and equipment inspections, coordinate scheduled preventive maintenance and testing with qualified external vendors, and maintain documentation for R&D and regulatory compliance.
  • Conduct routine eyewash and spill-station checks and coordinate annual preventive maintenance for emergency eyewash and safety-shower systems.
  • Manage the site pest-control program, including licensed-vendor coordination and service-record documentation.
  • Administer the Bloodborne Pathogen program, including maintaining the exposure-control plan, coordinating training, and managing post-exposure follow-up procedures for the research biology environment.
  • Plan, coordinate, and deliver annual EHS training for site personnel; ensure required curricula, including bloodborne pathogens and fire safety, are completed, documented, and retrievable for audits and inspections.
  • Maintain and renew the site's Controlled Substance License in compliance with DEA and applicable state requirements, including recordkeeping, inventory reconciliation, and reporting.
  • Coordinate and support annual fire-safety inspections, including scheduling, documentation preparation, and closure of findings, and maintain ongoing fire-extinguisher and suppression-system compliance.
  • Prepare and submit required OSHA year-end documentation, including OSHA 300, 300A, and 301 logs, and support related regulatory inquiries and inspections.
  • Author, review, and maintain EHS-related SOPs and supporting documents in the site quality-management system, aligning them with R&D requirements and participating in periodic reviews and change-control processes.
  • Support client audits and regulatory inspections by keeping EHS documentation, training records, waste manifests, and inspection logs current, organized, and retrievable.

Desired Qualifications

  • Certification in Safety (CSP), Industrial Hygiene (CIH), and/or Hazardous Materials Management (CHMM) is a plus.

About the Company

MedPharm

Topical and transdermal drug delivery CDMO

MedPharm is a contract development and manufacturing organization focused on topical, transdermal, and mucosal drug delivery. It provides end-to-end services from formulation development through clinical and commercial manufacturing, including analytical testing and regulatory support, and operates proprietary delivery platforms such as MedSpray, MedTherm, and AquaRMed to enable multiple administration routes. The company combines contract research with a patent portfolio and offers lifecycle support across development and manufacturing, differentiating itself from competitors. A July 2024 merger with Tergus Pharma expanded capabilities to include hormone-based and highly potent drugs, enhancing scale and scope with the aim of helping pharma and biotech move products from early formulation to scalable manufacturing.

Company size
Not listed
Company stage
Grant
Total funding
$390K
Headquarters
Guildford, United Kingdom
Founded
1999

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