General Information

Country United States

City Pennsville, New Jersey

Functional Area Operations

Job Group SHE

Employment Type Permanent Contract

Working time Full-time

Join Siegfried, a leading CDMO in the chemical and pharmaceutical manufacturing industry, as our Senior Safety and Health Manager. If you are passionate about safety and health management and ready to take on a leadership role within, we invite you to apply and contribute to Siegfried’s commitment to excellence and continuous improvement in workplace safety.

Your role

The incumbent is responsible for implementing the site’s safety, health, risk management and associated programs to achieve compliance with applicable regulations and working towards continuously improving the work environment to eliminate workplace injuries and illnesses.

  • Implement and manage the OSHA PSM and ChemStewards® programs.
  • Participate in pre-startup safety reviews and manage S&H programs to ensure regulatory compliance (OSHA, DOT, NFPA, TCPA).
  • Review Management of Change submittals for S&H requirements and lead the Industrial Hygiene program.
  • Oversee the Accident/Incident investigation program and conduct all safety and health training.
  • Lead the Emergency Response Team and audit S&H programs for compliance, reporting findings to departmental managers.
  • Manage the MSDS Program, PPE, and other safety-related equipment.
  • Ensure adherence to the Siegfried Code of Conduct and compliance with all SHE and cGMP regulations.

Your profile

Education and Experience:

  • BS/BA Degree in Safety & Health, Occupational Safety, Chemical Engineering, Chemistry, or a related field.
  • 7+ years of experience in the chemical and/or pharmaceutical manufacturing industry.
  • Knowledge of ChemStewards®, OSHA VPP, ISO, or other management systems is a plus.
  • CSP or CIH certification is a plus.

What We Are Looking For:

  • Ability to handle multiple tasks effectively.
  • Strong communication skills.
  • Strong leadership abilities.
  • Conscientious and detail-oriented.
  • Team player with a self-starter and initiator mindset.

Working at Siegfried

  • Competitive performance-based bonus 
  • A generous Employee Share Matching Plan 
  • 401(k) Match
  • Medical, Dental, and Vision (employee contributes a small cost) 
  • Life, Sickness and Accident insurance, and Long-term disability (paid by company) 
  • Buy Up of Life Insurance (optional)

Who we are

In the Midst of People’s Lives – Across the Globe

The Siegfried Group is one of the world’s leading Custom Development and Manufacturing Organizations (CDMOs) developing and producing active pharmaceutical ingredients (API), intermediates and finished dosage forms. As our core competence, we successfully integrate chemical and pharmaceutical capabilities into a single business model. 

The Siegfried name stands for highest quality, efficiency, flexibility and safety. Present in Europe, Asia and North America, we serve a broad global customer base from major international pharmaceutical companies down to small biologic-pharmaceutical organizations. For them we develop and produce product innovations on a large scale to finished products. We integrate our offer seamlessly into the customers’ value chain. Our comprehensive services range from early-stage Research & Development services such as synthesis, scale-up, formulation development, stability studies and method development all the way through to manufacturing services, ranging from preclinical R&D material for clinical trial purposes to commercial production. 

We are able to produce about 200 of the approximately 1500 registered drug substances used in medicine. Moreover, we produce 20 percent of global demand for caffeine. Consequently, nearly 1 billion individuals come into contact with Siegfried products.

What we do in Pennsville

Pennsville is our drug substance manufacturing site for the US mar-ket and provides spray drying operations globally.


Main activities

  • Pilot and commercial manufacturing of drug substances (APIs) and related intermediates
  • All fully cGMP and SHE compliant

Features

  • 3 GMP pilot suites: 0.1–2 m³ reactors
  • 200m3 commercial capacity: 1–10 m³ reactors
  • Successful transfer of new products to the commercial scale - Powerful rectification
  • Spray drying in pilot and commercial scale for both isolation and dispersion technology
  • Micronization in pilot and commercial

Strategic importance

  • CMO for innovative drug substances and manufacturer of our opiates portfolio for the US market