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- Aufgaben: Lead CAPEX projects in a commercial mammalian cell production line, ensuring compliance and operational excellence.
- Arbeitgeber: Join a key pharmaceutical client in Visp, Switzerland, making an impact in biopharmaceutical manufacturing.
- Mitarbeitervorteile: Enjoy a dynamic work environment with opportunities for professional growth and collaboration.
- Warum dieser Job: Be at the forefront of innovative projects that enhance production efficiency and quality standards.
- Gewünschte Qualifikationen: Bachelor’s or Master’s in Biochemical or Mechanical Engineering; 5+ years in biopharmaceutical project management required.
- Andere Informationen: Hands-on experience in GMP environments is essential; strong problem-solving and communication skills are a must.
Das voraussichtliche Gehalt liegt zwischen 72000 - 100000 € pro Jahr.
In partnership with our key pharmaceutical client in Visp, Switzerland, we are looking for a Technical Project Manager to play a critical role in overseeing the successful realization of CAPEX projects in a commercial mammalian cell production line.
ROLE
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Define the technical requirements and success criteria for the project, ensuring alignment with GMP standards, operational goals, and compliance expectations.
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Collaborate with stakeholders to integrate operational improvements into the overall project plan.
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Develop a comprehensive roadmap for the project lifecycle, from conceptual design through performance qualification (PQ).
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Act as the primary technical point of contact for the project, ensuring all mechanical adaptations and operational improvements meet required specifications.
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Coordinate with EPCM teams to ensure alignment of engineering deliverables with technical and operational requirements.
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Provide guidance and support to production staff implementing operational improvements.
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Ensure that all project activities comply with GMP regulations and internal quality standards.
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Collaborate with QA teams to manage GMP change control processes, including the preparation, review, and approval of Technical Change Requests (TCRs) and Change Records (CRs).
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Liaise with operations, maintenance, engineering, and quality teams to ensure seamless integration of mechanical adaptations into production.
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Facilitate communication and alignment between the production staff and the EPCM to address any technical challenges or deviations.
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Monitor the progress of technical and operational activities to ensure milestones are met on time and within budget.
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Conduct risk assessments and develop mitigation plans for potential project roadblocks.
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Provide regular updates and technical reports to project stakeholders.
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Lead the planning and execution of equipment commissioning, installation qualification (IQ), operational qualification (OQ), and performance qualification (PQ) activities.
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Oversee and coordinate with validation teams to ensure the effectiveness and reliability of the implemented changes.
PROFILE
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Bachelor’s or Master’s degree in Biochemical Engineering, Mechanical Engineering, Life Sciences, or a related field.
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5+ years of experience in biopharmaceutical manufacturing, with a strong focus on technical project management or operational excellence.
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Proven experience working on GMP-compliant projects, including change management and qualification activities.
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Hands-on experience in commissioning, qualification, and validation (CQV) of equipment and processes in a GMP environment.
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Strong knowledge of GMP regulations and biopharmaceutical manufacturing processes.
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Proficiency in project management tools and methodologies.
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Excellent problem-solving skills with the ability to manage technical challenges in a fast-paced environment.
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Effective communication and interpersonal skills to coordinate cross-functional teams.
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Detail-oriented with strong organizational skills for managing multiple workstreams.
Interested? Know someone that might be? Don’t hesitate to reach out on !
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Technical Project Manager Arbeitgeber: Panda International
Kontaktperson:
Panda International HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Technical Project Manager
✨Tip Number 1
Familiarize yourself with GMP regulations and biopharmaceutical manufacturing processes. Understanding these standards will not only help you in interviews but also demonstrate your commitment to compliance and quality.
✨Tip Number 2
Network with professionals in the biopharmaceutical industry, especially those who have experience in technical project management. Engaging with them can provide insights into the role and may even lead to referrals.
✨Tip Number 3
Prepare to discuss specific examples of your experience with commissioning, qualification, and validation (CQV) activities. Highlighting your hands-on experience will set you apart from other candidates.
✨Tip Number 4
Stay updated on the latest trends and technologies in biopharmaceutical manufacturing. Showing that you are proactive about learning can impress potential employers and demonstrate your passion for the field.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Technical Project Manager
Tipps für deine Bewerbung 🫡
Understand the Role: Make sure to thoroughly read the job description for the Technical Project Manager position. Understand the key responsibilities and required qualifications, especially the emphasis on GMP standards and project management in a biopharmaceutical context.
Tailor Your CV: Customize your CV to highlight relevant experience in biopharmaceutical manufacturing and technical project management. Emphasize your hands-on experience with commissioning, qualification, and validation processes, as well as any specific projects that align with the role.
Craft a Strong Cover Letter: Write a compelling cover letter that connects your background to the specific requirements of the job. Discuss your experience with GMP-compliant projects and how you have successfully managed cross-functional teams to achieve operational improvements.
Highlight Problem-Solving Skills: In your application, provide examples of how you've tackled technical challenges in previous roles. This will demonstrate your problem-solving abilities and readiness to handle the fast-paced environment described in the job listing.
Wie du dich auf ein Vorstellungsgespräch bei Panda International vorbereitest
✨Understand GMP Standards
Make sure you have a solid grasp of Good Manufacturing Practice (GMP) standards. Be prepared to discuss how your previous experiences align with these regulations and how you can ensure compliance in the projects you'll manage.
✨Showcase Your Project Management Skills
Highlight your experience with project management tools and methodologies. Be ready to provide examples of how you've successfully managed technical projects, particularly in biopharmaceutical manufacturing, and how you overcame challenges.
✨Prepare for Technical Questions
Expect to answer technical questions related to commissioning, qualification, and validation processes. Brush up on your knowledge of mechanical adaptations and operational improvements, as well as how they integrate into production lines.
✨Demonstrate Effective Communication
Since the role involves liaising with various teams, emphasize your communication skills. Prepare examples of how you've facilitated collaboration between cross-functional teams and resolved any technical challenges that arose during projects.
