Visp
6 months
41 hours
Start: February 3, 2025
Deadline: January 31, 2025
SL-000033
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.