CQV Engineer

Share: Information

• Location: Basel, Basel-City Switzerland
• Position: CQV Engineer
• Sector: Life Science
• Type of contract: Permanent contract
• Starting date: ASAP

agap2 is a European engineering and operational consulting group founded in 2005 and specialized in the industry. We work in the Pharma, Biotechnology, Medical Devices, Energy, Infrastructure, Transportation, Chemicals, and Information Technology sectors.

As a consultant, you will have to support our clients in the realization of their projects on site by bringing your expertise and your skills.

You are agile and eager to adapt to different work environments that will fuel your curiosity of seeing what’s behind closed doors of the biggest projects of our client’s portfolio.

Your main missions are:

As the Q&V Engineer you are primarily responsible for the preparation and the execution of the Commissioning, Qualification & Validation activities, including the following:

• Ensure milestone dates for commissioning and qualification are met. Prepare, execute, and approve Design Qualification (DQ) and release for Installation Qualification (IQ). Oversee commissioning, including vendor supervision and quality control.
• Prepare, execute, and approve Installation and Operational Qualification (OQ), and release for Operational Performance (OPS).
• Support DQ execution for other direct impact systems.
• Maintain control over activities and schedules for relevant systems.
• Report on key deliverables and align with project milestones.
• Assist in resolving project issues and maintaining non-conformance records.
• Evaluate project risks and the effectiveness of mitigation strategies.

This job is made for you if...

• Master or bachelor’s degree in chemical process, mechanical, pharmaceutical sciences or equivalent.
• 3+ years of years of experience in commissioning / qualification / validation (DQ, IQ, OQ, Commissioning) activities in the pharmaceutical/biotech environment.
• Preferably previous experience with Autoclaves qualification or clean rooms validation.
• GMP knowledge and knowledge of regulatory requirements.
• Fluent in German and English.

Working with us means...

Joining a group with strong development potential that aims to improve your employability on challenging and varied projects.

Joining a structure that has been established in Switzerland for a long time with a client portfolio that includes leaders in the sector.

Having a sustainable job with stability and access to a real collaboration.

Benefit from training with accredited and certified centers.

Having a local management team to support you in the achievement of your missions and in the development of your career.

Being part of a dynamic, committed team with real human values that we live by every day.

Thank you for your interest in this opportunity. Please note that only selected candidates will be contacted for an initial interview. In addition, only applications from Swiss and EU citizens can be considered. Please note that due to Brexit we are no longer accepting applications from the UK.