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Visp
6 months
41 hours
Start: February 3, 2025
Deadline: January 31, 2025

SL-000033

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SL-000033

Job description:

Your Responsibilities:

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.

About the customer:

Location: Visp

Contract Type: Contract

Duration: Until 16/07/2025

Start Date: ASAP

Workload: 100%

Requirements:

Your Background:

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:

What’s on Offer:

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

This role is handled by:

Veronika Nakev