M

MedPharm

Topical and transdermal drug delivery CDMO

Environmental Health & Safety Manager

Full-Time
No salary listed
Senior
Bachelor's, Master's
Durham, NC, USA
In Person
Facilities OperationsEnvironmental Health & Safety

About the job

Requirements
  • A minimum of 7 years of EHS-related experience within pharmaceutical manufacturing or research and development environments.
  • Working experience implementing EHS regulations, conducting incident investigations, and interacting with regulatory agencies and external organizations.
  • Experience conducting risk assessments and job hazard analyses for pharmaceuticals.
  • Experience administering and maintaining 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 research and development setting.
  • Demonstrated success exercising independent judgment, technical proficiency, scientific creativity, and collaboration in a current Good Manufacturing Practice environment.
  • Effective knowledge of applicable federal, state, and local regulations.
  • Familiarity with industry standards including the National Fire Protection Association, American National Standards Institute, American Conference of Governmental Industrial Hygienists, International Organization for Standardization, National Institute for Occupational Safety and Health, and American Society of Mechanical Engineers.
  • Familiarity with the Resource Conservation and Recovery Act, Clean Air Act, Clean Water Act, Nuclear Regulatory Commission, Environmental Protection Agency, Department of Environmental Protection, and Residual Waste Regulations.
Responsibilities
  • Develop and maintain environmental health and safety policies and procedures in compliance with state, federal, and local regulatory requirements and company standards.
  • Implement EHS programs and procedures and assess their impact on affected areas.
  • Perform tasks across multiple EHS disciplines and escalate compliance concerns to the management team based on risk exposure.
  • Analyze regulatory compliance data, including trending and presentation in management reviews.
  • Coordinate and conduct employee training in EHS programs.
  • Coordinate and conduct safety inspections and audits, and correlate inspection data with injury trends as needed.
  • Develop and manage an Emergency Response Program, including leading an Emergency Response Team.
  • Coordinate the Occupational Health and Ergonomics Programs.
  • Coordinate with regulators as the primary site contact and follow appropriate escalation procedures.
  • Lead the Material Risk Assessment program for all new compounds brought into United States sites and train impacted individuals on safe compound handling.
  • Maintain records necessary for compliance 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 relationships with stakeholders by developing rapport and understanding their needs and common goals.
  • Oversee accident and incident investigations and corrective actions.
  • Maintain EHS training documentation so it is readily retrievable for client audits and regulatory inspections.
  • Guide the incident response team and Site Safety Committee.
  • Lead the site's hazardous waste program and activities, including the introduction of new chemicals to the facility.
  • Lead regular site audits and risk assessment activities and track and manage timely implementation of corrective actions identified during audits or Failure Mode and Effects Analysis exercises.
  • Engage department leaders to develop and maintain safety training programs, ensuring training is documented, reviewed for effectiveness, compliance, and timeliness.
  • Independently manage disposal of experimental compounds and study samples, including chain-of-custody documentation and client-specific destruction requirements.
  • Perform routine waste management tasks, including biohazard waste pickups, chemical waste container management and pickups, broken glassware disposal, and oil waste collection.
  • Perform routine safety and equipment inspections and coordinate preventive maintenance and testing with qualified external vendors while maintaining compliance documentation.
  • Conduct eyewash and spill station checks and coordinate annual preventive maintenance for emergency eyewash and safety shower systems.
  • Manage the site pest control program, including vendor coordination and service-record documentation.
  • Administer the Bloodborne Pathogen program, including exposure control plan maintenance, training coordination, and post-exposure follow-up procedures.
  • Plan, coordinate, and deliver annual EHS training programs, ensuring required curricula such as bloodborne pathogens and fire safety are completed and documented.
  • 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, finding closure, and ongoing fire extinguisher and suppression system compliance.
  • Prepare and submit OSHA year-end documentation, including OSHA 300, 300A, and 301 logs, and support regulatory inquiries or inspections.
  • Author, review, and maintain EHS-related standard operating procedures and supporting documents within the site quality management system, including periodic review and change control.
  • Support client audits and regulatory inspections by maintaining current, organized, and retrievable EHS documentation, training records, waste manifests, and inspection logs.
Desired Qualifications
  • A master's or bachelor's degree in EHS, Occupational Health, Engineering, Science, or a closely related discipline, or equivalent technical experience plus demonstrated competence.
  • Certification in Safety (CSP), Industrial Hygiene (CIH), and/or Hazardous Materials Manager (CHMM).

About the company

MedPharm is a contract development and manufacturing organization specializing in 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. Its capabilities cover dermal, pulmonary, nasal, ophthalmic, and other mucosal routes, combining research services with a patent portfolio to support product lifecycle needs. In 2024 it merged with Tergus Pharma to expand into hormone-based and highly potent drugs, with the goal of helping pharmaceutical and biotech customers move from early formulation to scalable, reliable manufacturing for clinical and commercial use.

Company Size

N/A

Company Stage

Grant

Total Funding

$390K

Headquarters

Guildford, United Kingdom

Founded

1999

Simplify Jobs

Simplify's Take

What believers are saying

  • February 2025 CEO Bill Humphries signals post-merger growth execution and commercial discipline.
  • The Durham $4 million expansion created space for over 100 skilled hires in RTP.
  • Palvella's positive March 2026 Phase 3 readout and Purna partnership strengthen sponsor validation.

What critics are saying

  • MedPharm depends on niche topical spending; a sponsor slowdown hits utilization fast in 2025-2026.
  • The 2024 merger left some Tergus leaders exiting, creating integration and execution risk.
  • Topical CDMO giants and captive pharma plants can compress margins and steal repeat programs.

What makes MedPharm unique

  • MedPharm remains the topical and transepithelial CDMO specialist after the 2024 Tergus merger.
  • Durham and Guildford sites give MedPharm integrated development, clinical manufacturing, and commercial production.
  • August 2026 Olink CSP status adds proprietary proteomics beyond formulation and in vitro testing.

Help us improve and share your feedback! Did you find this helpful?

Company News

FinSMEs
Jul 9th, 2024
MedPharm and Tergus Pharma Merge

MedPharm, a Guildford, UK-based topical and transdermal Contract Development and Manufacturing Organization (CDMO) and Ampersand Capital Partners portfolio company, announced a merger with Tergus Pharma, a Research Triangle Park, NC-based end-to-end contract service provider and a Great Point Partners portfolio company

FinSMEs
Jul 8th, 2024
MedPharm and Tergus Pharma Merge

MedPharm, a UK-based CDMO, has merged with Tergus Pharma, a US-based contract service provider. The combined entity will operate under the MedPharm name, offering end-to-end drug development and manufacturing services. Michael Kane, Tergus Pharma CEO, will become CEO of MedPharm, while Patrick Walsh remains Executive Chairman. Great Point Partners retains a significant minority stake, with Ampersand Capital Partners and Bourne Partners Strategic Capital holding majority ownership.