The TPM is leading the technical project team to achieve project goals and milestones and is responsible for the development of the Basis of design and subsequently execute it until end of OQ. Role also acts as the SME of the design phase of the project, working with MSAT and Operations. Overall, the role supports the development of a project plan and schedule technical activities and works with the project controls team to manage the project budget and costs by helping to evaluate and mitigate project risks.
Responsibilities:
- The Technical Project Manager is responsible for ensuring that all technical deliverables are completed , equipment is installed and qualified, and that all documentation is completed and stored according to regulatory and industry standards.
- Responsible for the management and coordination of the Engineering, Construction, CQV, Operations and QA.
- The Technical Project Manager needs to coordinate the activities, project Team and documentation according to Project Schedule and Critical Path. A regular review of the schedule and targets will be coordinated by the TPM
- The Technical Project Manager must support the identification, evaluation, and mitigation of risks throughout the project lifecycle. They must have a clear understanding of the potential risks associated with the project and develop contingency plans to address them.
- Supporting the management of the project budget and control costs to ensure that the project stays within its financial constraints. This includes monitoring expenses, identifying cost-saving opportunities, and reporting on financial performance to stakeholders.
- The Technical Project Manager must be able to solve complex technical problems that arise during the project. This requires a deep understanding of the technical aspects of the project, as well as effective problem-solving skills and the ability to work collaboratively with cross-functional teams
Candidate Profile:
- Education: Bachelor or Master degree in Engineering (process, pharmaceutical, biochemical or equivalent)
- Experience
- 10+ years in project engineering and project management for chemical, biochemical, pharmaceutical industries with international experience.
- Broad technical knowledge of the Various Engineering Disciplines in the Pharmaceutical environment, both on clean and black utilities, process, automation, Instrumentation and Civil Engineering
- Task orientated person who is very comfortable working towards set objectives and has a track record of achieving results in this regard.
- Proven experience in scheduling related to investment projects .
- Experience in engineering aspects of facility design to build a compliant but cost effective plant.
- Knowledge of modern CQV approaches to minimize the time from construction completion to routine production while maintaining compliance.
- Excellent knowledge of computer systems (i.e. Microsoft Word, Excel, PowerPoint, and Visio).
- Good understanding of how the CDMO industry/business works.
- Experience at working both independently and in a team-oriented, collaborative environment is essential.
- Strong verbal and written communication skills (English and German).
- Effective influencing skills. Ability to communicate to varying levels and functions of the organization.
- Strong collaborative mindset.
- Proven ability to lead, mentor and coach direct reports and teams with or without direct line responsibility.
- Strong organizational skills, ability to balance multiple priorities simultaneously.
- Ability to solve problems, understanding details and strategic picture, providing practical solutions.
- Strong project management skills.
- Strong experience in Engineering and cGMP Manufacturing of chemical and biological APIs.
Key Skills
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- Posted
- Jul 28, 2025
- Type
- Contract
- Level
- Mid-Senior
- Location
- Stein
- Company
- Lonza
Industries
Categories
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3 roles aligned with this opportunity
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