Global Safety Governance and Compliance Manager

vor 2 Wochen

Zofingen, Schweiz Siegfried AG Vollzeit

Imagine leading the development, implementation, and continuous improvement of the SHE management system across all sites, ensuring every colleague returns home safe. As Global Safety Governance and Compliance Manager, you will strengthen the governance and compliance framework for Occupational Safety and Health while driving key initiatives to mitigate chemical process risks and machine safety.

This dynamic role can be based at any Siegfried European site, offering flexibility to work from either Spain, France, Germany, Switzerland, or Malta. It requires close collaboration with the Global SHE Team and approximately 40% travel.

Your role
  1. Lead SHE&S compliance programs, ensuring adherence to global standards, regulatory, insurance, and customer requirements through audits and site support.
  2. Success in this role is driven by your ability to empower teams, foster engagement, and drive sustainable improvements.
  3. Develop and oversee global SHE&S management systems aligned with ISO 45001/14001, establishing KPIs to track and report performance locally and globally for executive insights.
  4. Conduct root cause analyses for major incidents, guiding corrective and preventive actions in collaboration with site teams.
  5. Drive engagement with global safety programs (e.g., Passion for Zero, mySTOP Program, Life Saving Rules, Behavioral programs), ensuring adoption and evaluation for effectiveness.
  6. Collaborate with corporate sustainability teams to support climate goals and sustainability objectives.
  7. Act as a key point of contact for SHE&S events, ensuring swift resolution and escalation to corporate leadership when required.
Your profile

Experience:

  1. Our new colleague has spent more than 10 years in SHE&S roles, with at least 5 years in the Chemical manufacturing, oil & gas / Petrochemical, Biotechnology & Life Sciences, or other equivalent industries.
  2. An academic background in engineering, environmental science, occupational safety, or a related field will help you to understand topics.
  3. You have a strong understanding of pharmaceutical standards, including cGMP, GHS, REACH, and SHE&S implications in regulated environments, implementing and auditing ISO 45001 and ISO 14001.
  4. Knowledge of handling, storing, and transporting chemicals and hazardous materials in pharma settings. Proven expertise in HAZOP, FMEA, ATEX, process safety, fire protection, and SHE&S reporting, with strong analytical and redactional skills.
  5. Skilled in integrating SHE&S practices into lean manufacturing, Six Sigma, and safety management in pharma R&D, manufacturing, and maintenance environments.
  6. Business fluent English is important; any other European language is a plus.
  7. Strong communicator, simplifying complex SHE&S topics for diverse audiences while influencing senior leaders.
  8. Strategic problem-solver with adaptability to fast-paced, global, and highly regulated environments.

This role is available in Spain, France, Switzerland, Germany, or Malta. We expect our new colleague to travel 40% throughout the year.

Working at Siegfried
  1. Flexible working hours, allowing you to balance family, leisure, and work.
  2. Competitive salary and bonus.
  3. Employee Share Plan Participation.
  4. Opportunities for individual further training by arrangement.
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 Zofingen
  1. Development and commercial manufacture of active pharmaceutical ingredients (APIs) and corresponding intermediates.
  2. Fully compliant with cGMP and SHE (Safety, Health and Environmental) standards.
Special features
  1. Manufacture of high potency active ingredients in development and production.
  2. Micronization in development and production.
Strategic importance
  1. Contract manufacturing of new active ingredients.
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