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Technical Project Manager

Infos sur l'emploi

  • Annonce expirée
  • Taux d'activité :45%
  • Type de contrat :Temporaire
  • Lieu de travail :Visp

We are seeking a Technical Project Manager to lead capital investment projects in a GMP-regulated mammalian cell production line, driving…

Job description:

We are seeking a Technical Project Manager to lead capital investment projects in a GMP-regulated mammalian cell production line, driving initiatives from design to qualification.

About the customer:

The client is a leader in the Pharmaceutical industry, renowned for its innovative solutions and commitment to quality in healthcare.

Requirements:

Project Scope and Strategy Development:

  • Define project requirements, align with GMP standards, and integrate operational improvements.
  • Develop a roadmap covering design through performance qualification (PQ).

Technical Leadership:

  • Act as the primary technical contact, ensuring specifications are met.
  • Coordinate with EPCM teams and support production staff in operational improvements.

Quality and Compliance Oversight:

  • Ensure compliance with GMP regulations and manage change control processes with QA teams.

Cross-Functional Coordination:

  • Collaborate with operations, maintenance, engineering, and quality teams to integrate mechanical adaptations and resolve challenges.

Project Execution and Monitoring:

  • Track progress, address risks, and deliver regular updates to stakeholders.

Testing and Qualification:

  • Lead commissioning, installation (IQ), operational (OQ), and performance qualification (PQ) activities.

Competences:

Education:

  • Bachelor's or Master's degree in Biochemical Engineering, Mechanical Engineering, Life Sciences, or a related field.

Experience:

  • Minimum of 5 years' experience in biopharmaceutical manufacturing, with a focus on technical project management or operational excellence.
  • Proven track record in GMP-compliant projects, including change management and qualification activities.
  • Hands-on experience in commissioning, qualification, and validation (CQV) of equipment and processes.

Skills:

  • Strong knowledge of GMP regulations and biopharmaceutical manufacturing processes.
  • Proficiency in project management tools and methodologies.
  • Excellent problem-solving skills to manage technical challenges in a fast-paced environment.
  • Effective communication and interpersonal skills for coordinating cross-functional teams.
  • Detail-oriented with strong organizational skills for managing multiple workstreams

Compensation benefits:

  • Opportunity to contribute to impactful projects within a leading biopharmaceutical organization.
  • A collaborative and innovative work environment.
  • Professional growth and development opportunities.

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