General Information

Country United States

City Grafton, Wisconsin

Functional Area Operations

Job Group Site Management

Employment Type Permanent Contract

Working time Full-time

The Siegfried Group is a global life science company with a network of 13 sites across Europe, the USA, and Asia. Siegfried offers contract development and manufacturing of active pharmaceutical ingredients, intermediates, and drug products. Siegfried employs over 3,700 people and generated sales of 1.3 billion USD in 2023. Siegfried Holding AG is listed on the SIX Swiss Exchange (SIX: SFZN). 

Siegfried's Acceleration Hub is the latest addition to the Siegfried network. Located in Grafton (WI), we provide comprehensive support to customers in from early phase pre-clinical and clinical development, through scale up and validation up to and including commercial manufacturing of Drug Substances.

Within this context, we are currently looking to fill the position of Director Project Management to join a highly motivated, hands-on Site Leadership Team who is ‘all in’, growing to double new chemical entity capacity in the next two years with both facility and technology expansions. 

Your role

In this role you will be responsible for the overall strategy and execution of New Chemical Entities introduction and lifecycle management by providing project management leadership and management for projects evaluated and accepted by the Siegfried Acceleration Hub. This includes internal and external technical transfer projects, product development and potentially commercialization projects, as well as process improvement projects for the Grafton Site. In addition, you will have the chance to lead and further build up the newly set up project management team.

This role is an integral part of the Site Leadership Team and reports directly to the General Manager of the site.

Your tasks:

  • Lead and manage cross-functional project teams, coordinating activities across departments to ensure timely, quality, and budget-conscious project delivery from early phase to commercialization.
  • Collaborate closely with Business Development/Sales to secure new clients, support technical evaluations, review proposals, and contribute to customer questionnaires and inquiries.
  • Serve as the primary contact for client projects, including handling project changes (scope, schedule, and budget), preparing necessary documentation, and leading customer communications.
  • Drive internal and external meetings by setting agendas, tracking progress, issuing minutes, and ensuring action items are completed by deadlines.
  • Prepare and update detailed project plans, establish milestones, identify critical issues, and proactively implement solutions to mitigate risks.
  • Oversee project-related customer site visits during bidding and manufacturing, ensuring successful client engagement and satisfaction.
  • Act as a working manager by leading a team of Project Managers, providing direction and supporting their development and project success.

Your profile

  • Master's degree in Organic Chemistry, Engineering, or a related life sciences field required; PhD preferred.
  • 12-15+ years of experience in the pharmaceutical industry, with expertise in project management, matrix management, and team leadership.
  • Deep knowledge of pharmaceutical drug substance development, API manufacturing, Good Manufacturing Practices (GMPs), and ICH standards (e.g., Q7A).
  • Project Management certification (e.g., PMI, PMP) or equivalent experience strongly preferred.
  • Strong leadership skills with the ability to influence, guide, and manage teams to meet project timelines, budget commitments, and desired outcomes.
  • Experience managing multiple projects simultaneously and working directly with clients to exceed expectations.
  • Excellent communication skills, both verbal and written, with the ability to work cross-functionally across diverse teams and cultures.
  • Highly detail-oriented, self-motivated, and capable of working independently with minimal supervision.

Working at Siegfried

Siegfried's work environment is dynamic and international. With a highly professional and motivated team, the company operates in a future-oriented business field. Siegfried possesses a unique culture that leverages cultural differences to create a competitive advantage. Siegfried places highest priority on providing a flexible, diverse and discrimination-free working environment in which employees can develop personally and professionally, advance innovation and deliver superior performance. We strive to provide a work environment where employees can take on challenging jobs and associated responsibilities that best serve their personal and technical development and can benefit from the success of our company. The company regulations in respect of compensation and career development opportunities apply to all Siegfried sites. Additional conditions of employment are governed by location-specific circumstances, legislation and customs.

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 Grafton

The Siegfried Acceleration Hub in Grafton specializes in early-phase development and manufacturing services, including services for projects with highly potent APIs.


Competencies

·         Early-phase development and manufacturing



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