Project Manager, Neuchâtel

Vor 2 Tagen

Neuenburg, Schweiz TN Switzerland Vollzeit

CK QLS are recruiting for a highly skilled and experienced Project Manager, to join our client based in Neuchâtel on a 12 month contract basis. The successful candidate will be responsible for driving continuous improvement and optimization of business processes across all departments, collaborating with cross-functional partners to implement enhancements and improvements, and acting as a change champion to facilitate transformation.

Responsibilities:

  1. Provide expertise in business process management and modeling, ensuring alignment with the company's Business Process Architecture.
  2. Identify, map, and document current business processes, analyze for inefficiencies, and redesign processes to enhance efficiency and reduce costs.
  3. Develop agile and adaptable processes that can quickly respond to new opportunities or shifts in the industry landscape.
  4. Collaborate with colleagues to integrate new technologies, such as AI/ML and automation, into business processes.
  5. Establish metrics and KPIs to monitor the efficiency and effectiveness of newly implemented processes.
  6. Lead change management to ensure that changes in business processes are accepted and effectively implemented across the organization.

Qualifications:

  1. Minimum of 5+ years of experience in a manufacturing or operations management role, with a strong focus on Business Process Management and Business Process Reengineering (BPR), Operational Excellence, Continuous Improvement, or Lean Manufacturing.
  2. Bachelor’s degree in a technical field or equivalent work experience.
  3. Strong financial and business management acumen with an eye for identifying opportunities to achieve efficiencies.
  4. Experience managing cross-functional teams and driving projects from inception to successful completion.
  5. Excellent communication, leadership, coaching, and interpersonal skills, with the ability to influence and engage employees at all levels.
  6. Fluency in French and English language.
  7. A master's degree (MBA or M.Sc.).
  8. Knowledge of manufacturing software (e.g., SAP, MES, Minitab, etc.) and Business Process Management software.
  9. Experience in working with Pharmaceutical cGMP, regulatory compliance, and quality systems in a manufacturing environment.

Day-to-day:

The successful candidate will work on-site with daily interactions with manufacturing teams and cross-functional departments, and will be required to gown into ISO space. Occasional travel may be required to other sites or company locations.

Benefits:

  1. Competitive salary and benefits package.
  2. Opportunity to work in a dynamic and collaborative environment.
  3. Professional development and growth opportunities.
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